Salbutamol
Regulatory milestones approvals, filings & regulatory actions · 14 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Label expansion | US (FDA) | PROAIR RESPICLICK | — | 2016-04-28 | fda.gov ↗ |
| Label expansions (2) | US (FDA) | PROAIR HFA | — | 2006-02-03 – 2008-09-16 | fda.gov ↗ |
| Label expansion | US (FDA) | VENTOLIN HFA | — | 2008-03-26 | fda.gov ↗ |
| Label expansions (2) | US (FDA) | PROVENTIL-HFA | — | 1998-09-23 – 1999-06-02 | fda.gov ↗ |
| Label expansion | US (FDA) | VOLMAX | — | 1997-10-08 | fda.gov ↗ |
| Label expansions (3) | US (FDA) | PROVENTIL | — | 1984-09-13 – 1997-09-18 | fda.gov ↗ |
| Label expansions (3) | US (FDA) | VENTOLIN | — | 1990-09-24 – 1997-06-16 | fda.gov ↗ |
| Approved | US (FDA) | VENTOLIN | — | 1981-05-01 | fda.gov ↗ |
Trials 199 · started per year
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 05 trials | ||||||
| Phase 0 | NCT07591558 | Jun → Oct 2026 expected | diabetes mellitus, lung disorder | King Abdullah University Hospital | Not yet recruiting | No outcome recorded |
| Phase 0 | NCT06319183 | Mar → Jun 2024 | — | Tongji University | Unknown | No outcome recorded |
| Phase 0 | NCT06139029 | Nov 2022 → Mar 2023 | acute bronchiolitis | Mardan Medical Complex | Completed | No outcome recorded |
| Phase 0 | NCT03889379 | Jan 2019 → Jun 2021 | — | University of Arizona | Withdrawn | No outcome recorded |
| Phase 0 | NCT02135965 | Apr 2009 → Aug 2011 | — | Pennington Biomedical Research Center | Completed | No outcome recorded |
| Phase 129 trials | ||||||
| Phase 1 | NCT06514157 | Aug → Sep 2024 | — | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT06433921 | Aug 2024 → Feb 2027 expected | asthma | GlaxoSmithKline | Recruiting | No outcome recorded |
| Phase 1 | NCT06921291 | Aug → Dec 2024 | — | Khyber Teaching Hospital | Completed | No outcome recorded |
| Phase 1 | NCT06433908 | Jun → Oct 2024 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT06290102 | May → Oct 2024 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT06271408 | Feb → Apr 2024 | chronic obstructive pulmonary disease | Polarean, Inc. | Unknown | No outcome recorded |
| Phase 1 | NCT06027606 | Sep 2023 → Sep 2025 | — | University of Alberta | Completed | No outcome recorded |
| Phase 1 | NCT05791565 | Apr → May 2023 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT03436225 | Feb 2019 | respiratory syncytial virus bronchiolitis | Assiut University | Unknown | No outcome recorded |
| Phase 1 | NCT03772223 | Jan → May 2019 | — | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT03514615 | Jan → Jul 2018 | — | University Hospitals, Leicester | Completed | No outcome recorded |
| Phase 1 | NCT03373409 | Nov 2017 → May 2018 | asthma | Concentrx Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT03098680 | Apr 2017 → Feb 2020 | cardiovascular disorder | Cambridge University Hospitals NHS Foundation Trust | Terminated | No outcome recorded |
| Phase 1 | NCT03480997 | Dec 2016 → Apr 2017 | chronic obstructive pulmonary disease | Pneuma Respiratory, Inc | Completed | No outcome recorded |
| Phase 1 | NCT02566252 | Jul 2015 → Jan 2016 | — | Pulmotect, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT01984086 | Oct 2013 → May 2014 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT01895998 | Aug 2013 → Apr 2014 | sickle cell disease | Duke University | Completed | No outcome recorded |
| Phase 1 | NCT01844401 | Apr → Aug 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT01859624 | Jun 2012 → Apr 2013 | glycogen storage disease due to acid maltase deficiency, late-onset | Duke University | Completed | No outcome recorded |
| Phase 1 | NCT01457261 | Apr 2012 → Nov 2014 | idiopathic pulmonary fibrosis | Royal Brompton & Harefield NHS Foundation Trust | Completed | No outcome recorded |
| Phase 1 | NCT01263197 | Dec 2010 → Mar 2011 | major depressive disorder | Eli Lilly and Company | Completed | No outcome recorded |
| Phase 1 | NCT01203592 | Sep 2010 → Aug 2013 | congenital myasthenic syndrome | Mayo Clinic | Completed | No outcome recorded |
| Phase 1 | NCT02207452 | Aug 2010 → Jul 2011 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT01056159 | Jan → Jun 2010 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT00674050 | May → Sep 2008 | diabetes mellitus | Mannkind Corporation | Completed | No outcome recorded |
| Phase 1 | NCT00549120 | Aug → Oct 2007 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT00649987 | Sep → Oct 2005 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT00649779 | Sep → Oct 2005 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT02173678 | Oct → Nov 1999 | — | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 1/22 trials | ||||||
| Phase 1/2 | NCT01799538 | Jun 2013 → Nov 2027 expected | lymphangioleiomyomatosis | National Heart, Lung, and Blood Institute (NHLBI) | Recruiting | No outcome recorded |
| Phase 1/2 | NCT01885936 | Jun 2013 → Dec 2016 | glycogen storage disease II | Duke University | Completed | No outcome recorded |
| Phase 222 trials | ||||||
| Phase 2 | NCT06644924 | Feb → Jun 2025 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT05860244 | Sep 2024 → Jul 2025 | amyotrophic lateral sclerosis | Assistance Publique - Hôpitaux de Paris | Unknown | No outcome recorded |
| Phase 2 | NCT03643874 | Jun → Aug 2018 | asthma | Concentrx Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT03371459 | Dec 2017 → Mar 2018 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT03364608 | Dec 2017 → Mar 2018 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT03270332 | Oct 2017 → Jul 2020 | pulmonary hypertension | University of Miami | Completed | No outcome recorded |
| Phase 2 | NCT02542254 | Oct → Dec 2015 | chronic obstructive pulmonary disease | Verona Pharma, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01957293 | Oct 2013 → Jan 2014 | — | University of Basel | Completed | No outcome recorded |
| Phase 2 | NCT01252758 | Nov 2012 → Apr 2013 | asthma | Acerus Pharmaceuticals Corporation | Withdrawn | No outcome recorded |
| Phase 2 | NCT01581177 | Apr → Jul 2012 | asthma | Amphastar Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01958814 | Feb 2012 → Jul 2015 | respiratory failure | University Hospital, Tours | Completed | No outcome recorded |
| Phase 2 | NCT01470755 | Jan 2012 → Jan 2014 | asthma | Assistance Publique - Hôpitaux de Paris | Completed | No outcome recorded |
| Phase 2 | NCT01189396 | Jul → Dec 2010 | asthma, chronic obstructive pulmonary disease | Amphastar Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01174732 | Jul → Oct 2010 | asthma | Amphastar Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01058863 | Feb → Jun 2010 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT00818454 | Dec 2008 → Sep 2009 | asthma | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2 | NCT00696540 | Jun → Sep 2008 | bronchiolitis | University Diego Portales | Unknown | No outcome recorded |
| Phase 2 | NCT00310401 | Apr 2007 → May 2011 | pulmonary edema | Vanderbilt University Medical Center | Completed | No outcome recorded |
| Phase 2 | NCT00358488 | Apr 2006 → Jan 2007 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 2 | NCT00320034 | Apr 2006 → Jun 2008 | asthma | Hamilton Health Sciences Corporation | Completed | No outcome recorded |
| Phase 2 | NCT00096616 | Nov 2004 → Mar 2006 | asthma | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2 | NCT02182674 | Oct 2000 → Aug 2001 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2/34 trials | ||||||
| Phase 2/3 | NCT06815679 | Mar 2025 → Jan 2026 overdue | acute respiratory failure, pneumonia | Università degli Studi di Ferrara | Not yet recruiting | No outcome recorded |
| Phase 2/3 | NCT03914638 | Apr 2019 → Oct 2021 | generalized myasthenia gravis | University of Aarhus | Unknown | No outcome recorded |
| Phase 2/3 | NCT01375361 | Apr 2009 → Jul 2010 | congestive heart failure | University of California, San Francisco | Withdrawn | No outcome recorded |
| Phase 2/3 | NCT00755079 | Apr 2007 → Aug 2012 | spinal cord injury | US Department of Veterans Affairs | Completed | No outcome recorded |
| Phase 348 trials | ||||||
| Phase 3 | NCT06664619 | Dec 2024 → Sep 2026 expected | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Recruiting | No outcome recorded |
| Phase 3 | NCT06471257 | Jun 2024 → Oct 2026 expected | asthma | AstraZeneca | Recruiting | No outcome recorded |
| Phase 3 | NCT06307665 | May 2024 → Oct 2027 expected | asthma | AstraZeneca | Recruiting | No outcome recorded |
| Phase 3 | NCT06245551 | Dec 2023 → Jun 2024 | exercise-induced bronchoconstriction | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT06154304 | Dec 2023 → Sep 2024 | asthma | Cipla Ltd. | Completed | No outcome recorded |
| Phase 3 | NCT05653024 | Jul 2023 → May 2025 | food allergy | Philippe Bégin | Terminated | No outcome recorded |
| Phase 3 | NCT05505734 | Sep 2022 → Aug 2024 | asthma | Bond Avillion 2 Development LP | Completed | No outcome recorded |
| Phase 3 | NCT06946264 | Jul 2022 → Dec 2029 expected | bronchiolitis | Nemours Children's Clinic | Recruiting | No outcome recorded |
| Phase 3 | NCT04234464 | Jan → Aug 2020 | exercise-induced bronchoconstriction | Bond Avillion 2 Development LP | Completed | No outcome recorded |
| Phase 3 | NCT03449056 | Jan 2019 → Jan 2020 | chronic obstructive pulmonary disease | Poitiers University Hospital | Unknown | No outcome recorded |
| Phase 3 | NCT03528577 | Sep 2018 → Mar 2019 | asthma | Sun Pharmaceutical Industries, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT03816267 | May 2018 → Mar 2019 | asthma | Suez Canal University | Completed | No outcome recorded |
| Phase 3 | NCT03256695 | Sep 2017 → Apr 2018 | chronic obstructive pulmonary disease | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT03169504 | May 2017 → May 2018 | chronic obstructive pulmonary disease | Henan University of Traditional Chinese Medicine | Unknown | No outcome recorded |
| Phase 3 | NCT02969408 | Feb 2017 → Feb 2018 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT03208894 | Nov 2016 → May 2017 | persistent tachypnoe of infancy, usual | Armed Forces Hospital, Pakistan | Completed | No outcome recorded |
| Phase 3 | NCT02885636 | Sep 2016 → Sep 2017 | left ventricular failure | Mayo Clinic | Completed | No outcome recorded |
| Phase 3 | NCT02782052 | Jul 2016 → Oct 2018 | pulmonary arterial hypertension | Assistance Publique - Hôpitaux de Paris | Withdrawn | No outcome recorded |
| Phase 3 | NCT02160548 | Apr → Dec 2015 | organophosphate poisoning | Sylhet M.A.G.Osmani Medical College | Completed | No outcome recorded |
| Phase 3 | NCT02126839 | May 2014 → Feb 2015 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01836016 | May 2013 → May 2015 | chronic obstructive pulmonary disease | Henan University of Traditional Chinese Medicine | Unknown | No outcome recorded |
| Phase 3 | NCT01857323 | May → Aug 2013 | asthma, chronic obstructive pulmonary disease | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01791972 | Mar → May 2013 | exercise-induced bronchoconstriction | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01424813 | Dec 2012 → Oct 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01747629 | Dec 2012 → Oct 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01698320 | Oct 2012 → Dec 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01218009 | Oct → Dec 2010 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Terminated | No outcome recorded |
| Phase 3 | NCT01095016 | Mar 2010 → Sep 2012 | asthma | Taiwan Otsuka Pharm. Co., Ltd | Completed | No outcome recorded |
| Phase 3 | NCT01096017 | Mar → Apr 2010 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT01076322 | Mar 2009 → Jun 2010 | asthma | Taiwan Otsuka Pharm. Co., Ltd | Completed | No outcome recorded |
| Phase 3 | NCT00669617 | Apr → Aug 2008 | chronic obstructive pulmonary disease | Novartis | Completed | No outcome recorded |
| Phase 3 | NCT00634517 | Mar → Dec 2008 | asthma | Amphastar Pharmaceuticals, Inc. | Terminated | No outcome recorded |
| Phase 3 | NCT00634829 | Feb → Oct 2008 | exercise-induced bronchoconstriction | Amphastar Pharmaceuticals, Inc. | Terminated | No outcome recorded |
| Phase 3 | NCT00528723 | Nov 2007 → Jan 2009 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 3 | NCT00635505 | Sep 2007 → Aug 2008 | asthma | Amphastar Pharmaceuticals, Inc. | Terminated | No outcome recorded |
| Phase 3 | NCT00577655 | Aug 2007 → Jul 2008 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT00990847 | Jun 2007 → Apr 2008 | acute asthma | PT Otsuka Indonesia | Completed | No outcome recorded |
| Phase 3 | NCT00462540 | May → Sep 2007 | chronic obstructive pulmonary disease | Dey | Completed | No outcome recorded |
| Phase 3 | NCT00400153 | Nov 2006 → Apr 2008 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00308685 | Jun → Dec 2006 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT00252863 | Dec 2004 → May 2006 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00144846 | Sep 2004 → Feb 2006 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT00085774 | Jun → Sep 2004 | exercise-induced bronchoconstriction | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02177253 | Oct 2002 → Mar 2004 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00382889 | Aug 2002 → Sep 2004 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 3 | NCT00665600 | Feb 2002 → Mar 2003 | chronic obstructive pulmonary disease | Sumitomo Pharma America, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02182700 | Jul 1998 → Dec 1999 | asthma | Boehringer Ingelheim | Terminated | No outcome recorded |
| Phase 3 | NCT00000577 | Sep 1993 → Jul 2008 | asthma, lung disorder | Milton S. Hershey Medical Center | Withdrawn | No outcome recorded |
| Phase 445 trials | ||||||
| Phase 4 | NCT07426458 | Apr 2026 → Apr 2028 expected | asthma | University of Miami | Recruiting | No outcome recorded |
| Phase 4 | NCT07166939 | Nov 2025 → Jun 2027 expected | acute asthma | Massachusetts General Hospital | Recruiting | No outcome recorded |
| Phase 4 | NCT06825013 | Nov 2024 → Jan 2027 expected | chronic obstructive pulmonary disease | Dr. J. Alberto Neder | Recruiting | No outcome recorded |
| Phase 4 | NCT06563102 | Sep 2024 → Feb 2026 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT06158893 | Aug 2024 → Aug 2025 | — | Assiut University | Unknown | No outcome recorded |
| Phase 4 | NCT06422689 | May 2024 → Feb 2027 expected | asthma | AstraZeneca | Active not recruiting | No outcome recorded |
| Phase 4 | NCT04184609 | Jul → Nov 2023 | childhood onset asthma, obesity disorder | Ohio State University | Withdrawn | No outcome recorded |
| Phase 4 | NCT05084222 | Nov 2021 → Jun 2023 | asthma | Orion Corporation, Orion Pharma | Completed | No outcome recorded |
| Phase 4 | NCT05087693 | Nov 2021 → Aug 2023 | bronchial disorder | University of British Columbia | Completed | No outcome recorded |
| Phase 4 | NCT04677959 | Feb 2021 → Mar 2022 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 4 | NCT04606394 | Dec 2020 → Dec 2021 | chronic obstructive pulmonary disease | Pulmonary Research Institute of Southeast Michigan | Completed | No outcome recorded |
| Phase 4 | NCT03890666 | Oct 2020 → Oct 2021 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 4 | NCT04012138 | Dec 2019 → Dec 2025 | — | Nantes University Hospital | Completed | No outcome recorded |
| Phase 4 | NCT04207840 | Dec 2019 | anaphylaxis, asthma | Amphastar Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 4 | NCT03924635 | Aug 2019 → Dec 2022 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT03586544 | Sep 2018 → Mar 2020 | childhood onset asthma, exercise-induced bronchoconstriction, obesity disorder | University of Nevada, Las Vegas | Terminated | No outcome recorded |
| Phase 4 | NCT02966184 | Sep → Oct 2018 | status asthmaticus | Norton Healthcare | Terminated | No outcome recorded |
| Phase 4 | NCT03493503 | Apr 2017 → May 2019 | status asthmaticus | Erasmus Medical Center | Completed | No outcome recorded |
| Phase 4 | NCT02914652 | Oct 2016 → Jul 2017 | ventricular septal defect | University of Aarhus | Completed | No outcome recorded |
| Phase 4 | NCT03044938 | Aug 2016 | asthma | Ibirapuera University | Completed | No outcome recorded |
| Phase 4 | NCT02797275 | Jun 2016 → Dec 2026 expected | obstructive lung disease | University of California, San Francisco | Active not recruiting | No outcome recorded |
| Phase 4 | NCT03199976 | Apr 2016 → Nov 2020 | asthma, bronchitis, obstructive lung disease | Helsinki University Central Hospital | Terminated | No outcome recorded |
| Phase 4 | NCT02447250 | Oct 2013 → Dec 2014 | bronchopulmonary dysplasia | Oregon Health and Science University | Completed | No outcome recorded |
| Phase 4 | NCT02405598 | Oct 2013 → Jul 2015 | glycogen storage disease due to acid maltase deficiency, infantile onset | National Taiwan University Hospital | Completed | No outcome recorded |
| Phase 4 | NCT01903785 | May 2013 → Dec 2014 | exercise-induced bronchoconstriction | University of British Columbia | Completed | No outcome recorded |
| Phase 4 | NCT01721291 | Oct 2012 → Nov 2017 | asthma, chronic obstructive pulmonary disease | Imperial College London | Completed | No outcome recorded |
| Phase 4 | NCT02103374 | Jan 2012 → Dec 2015 | chronic obstructive pulmonary disease | University Hospital, Tours | Completed | No outcome recorded |
| Phase 4 | NCT01112241 | Apr → May 2010 | transplant-related bronchiolitis obliterans | IRCCS Azienda Ospedaliera Universitaria San Martino - IST Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy | Completed | No outcome recorded |
| Phase 4 | NCT02877537 | Oct 2008 → Apr 2012 | asthma | Central Hospital, Nancy, France | Completed | No outcome recorded |
| Phase 4 | NCT00783250 | Sep 2008 → Aug 2011 | chronic obstructive pulmonary disease | IRCCS Azienda Ospedaliero-Universitaria di Bologna | Terminated | No outcome recorded |
| Phase 4 | NCT00440245 | Feb 2007 → Jul 2010 | asthma, chronic obstructive pulmonary disease | University of Saskatchewan | Completed | No outcome recorded |
| Phase 4 | NCT00388882 | Oct 2006 → Oct 2007 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00385359 | Oct 2006 → ? | asthma | University Health Network, Toronto | Unknown | No outcome recorded |
| Phase 4 | NCT00359788 | Jul 2006 → Apr 2008 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00354354 | Mar 2006 → Jul 2009 | chronic obstructive pulmonary disease | Queen's University | Completed | No outcome recorded |
| Phase 4 | NCT00273689 | Dec 2005 → Sep 2007 | exercise-induced bronchoconstriction | University of New Mexico | Completed | No outcome recorded |
| Phase 4 | NCT00325767 | May 2004 → Sep 2005 | mucus inspissation of respiratory tract | Johns Hopkins University | Completed | No outcome recorded |
| Phase 4 | NCT00272753 | Apr 2004 → Nov 2005 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT07436104 | Jan 2004 → Dec 2015 | asthma, chronic diarrheal disease, chronic obstructive pulmonary disease, hypertensive disorder +2 | MAHAN Trust | Completed | No outcome recorded |
| Phase 4 | NCT00273962 | May 2002 → Nov 2003 | asthma | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00361452 | Dec 2000 → May 2001 | respiratory syncytial virus bronchiolitis | Rambam Health Care Campus | Terminated | No outcome recorded |
| Phase 4 | NCT02235428 | Sep 1998 | asthma | Boehringer Ingelheim | Terminated | No outcome recorded |
| Phase 4 | NCT02182713 | May → Sep 1998 | asthma | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT02182856 | Feb 1998 → Jul 2000 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 4 | NCT00940927 | Jul 1993 → Oct 1994 | asthma | Nemours Children's Clinic | Completed | No outcome recorded |
| Phase not applicable44 trials | ||||||
| — | NCT07378605 | Jan → Mar 2026 overdue | — | Saglik Bilimleri Universitesi Gazi Yasargil Training and Research Hospital | Not yet recruiting | No outcome recorded |
| — | NCT06426082 | Nov 2024 → Aug 2025 overdue | cardiovascular-kidney-metabolic syndrome | Universidad de Almeria | Not yet recruiting | No outcome recorded |
| — | NCT06276231 | Jul 2024 → Mar 2026 | urinary tract obstruction | Oman Medical Speciality Board | Unknown | No outcome recorded |
| — | NCT06754631 | Apr → Sep 2024 | childhood onset asthma | Muhammad Aamir Latif | Completed | No outcome recorded |
| — | NCT05932316 | May 2023 → Apr 2024 | bronchiectasis, bronchiolitis, cystic fibrosis, immunodeficiency disease +1 | Rambam Health Care Campus | Unknown | No outcome recorded |
| — | NCT05914285 | Apr 2023 → Jun 2025 overdue | chronic obstructive pulmonary disease | Yonsei University | Active not recruiting | No outcome recorded |
| — | NCT05786950 | Jan → Jul 2023 | chronic obstructive pulmonary disease | The First Affiliated Hospital of Guangzhou Medical University | Completed | No outcome recorded |
| — | NCT05589441 | Oct 2022 → Oct 2023 | — | First Affiliated Hospital Xi'an Jiaotong University | Unknown | No outcome recorded |
| — | NCT04912596 | Aug 2022 → Jan 2025 overdue | asthma | Intech Biopharm Ltd. | Recruiting | No outcome recorded |
| — | NCT04402658 | Aug 2022 → May 2023 | substance abuse | Norwegian School of Sport Sciences | Withdrawn | No outcome recorded |
| — | NCT05241288 | Mar 2022 → Feb 2023 | chronic obstructive pulmonary disease | University of North Carolina, Chapel Hill | Completed | No outcome recorded |
| — | NCT04914273 | Jun → Aug 2021 | — | Fraunhofer-Institute of Toxicology and Experimental Medicine | Completed | No outcome recorded |
| — | NCT04615611 | Nov 2020 → Nov 2021 | — | University of Copenhagen | Unknown | No outcome recorded |
| — | NCT04558190 | Sep 2020 → Nov 2021 | — | University of Copenhagen | Completed | No outcome recorded |
| — | NCT03524066 | Apr → Dec 2018 | — | Fraunhofer-Institute of Toxicology and Experimental Medicine | Completed | No outcome recorded |
| — | NCT03091504 | Sep 2017 → Mar 2018 | — | Rush University Medical Center | Completed | No outcome recorded |
| — | NCT03071731 | Apr 2017 → Jun 2019 | chronic obstructive pulmonary disease | Laval University | Unknown | No outcome recorded |
| — | NCT03271905 | Apr 2017 → Dec 2018 | asthma, chronic obstructive pulmonary disease | Federal University of Rio Grande do Norte | Unknown | No outcome recorded |
| — | NCT02925130 | Oct 2016 → Sep 2017 | — | University Hospital, Grenoble | Completed | No outcome recorded |
| — | NCT02818270 | Jun → Dec 2016 | chronic obstructive pulmonary disease | Chang Gung University | Completed | No outcome recorded |
| — | NCT02740660 | Apr 2016 → Oct 2017 | — | Pennington Biomedical Research Center | Completed | No outcome recorded |
| — | NCT02678949 | Mar → Aug 2016 | childhood onset asthma | Hospital Infantil de Mexico Federico Gomez | Unknown | No outcome recorded |
| — | NCT02802111 | Jun 2015 → Sep 2017 | — | Children's Hospital Los Angeles | Completed | No outcome recorded |
| — | NCT02296047 | Dec 2014 → May 2015 | chronic obstructive pulmonary disease | Zhujiang Hospital | Completed | No outcome recorded |
| — | NCT03062904 | Feb 2014 → Dec 2019 | — | Assistance Publique - Hôpitaux de Paris | Unknown | No outcome recorded |
| — | NCT02551276 | Nov 2013 → Nov 2014 | upper limb hypertrophy | University of Copenhagen | Completed | No outcome recorded |
| — | NCT02218398 | May 2013 → Jun 2015 | chronic obstructive pulmonary disease | Beijing Chao Yang Hospital | Unknown | No outcome recorded |
| — | NCT01655199 | Sep 2012 → Jul 2014 | chronic obstructive pulmonary disease | Laval University | Unknown | No outcome recorded |
| — | NCT01799109 | Nov 2011 → Jan 2012 | asthma | Chongqing Medical University | Completed | No outcome recorded |
| — | NCT01323010 | Sep 2011 → Dec 2013 | asthma | University of Sao Paulo | Completed | No outcome recorded |
| — | NCT01521572 | Jun 2011 → Jan 2012 | obstructive lung disease | Rio de Janeiro State University | Unknown | No outcome recorded |
| — | NCT01255449 | Dec 2010 → Mar 2012 | disease related to hematopoietic stem cell transplant, transplant-related bronchiolitis obliterans | IRCCS Azienda Ospedaliera Universitaria San Martino - IST Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy | Completed | No outcome recorded |
| — | NCT01196377 | Sep → Oct 2010 | acute asthma | Vanderbilt University Medical Center | Completed | No outcome recorded |
| — | NCT01067534 | Feb 2010 → Jan 2011 | isoproterenol-mediated vasodilatation | University of Patras | Completed | No outcome recorded |
| — | NCT01880723 | May 2009 → Jul 2012 | cystic fibrosis | University of Arizona | Completed | No outcome recorded |
| — | NCT00498251 | Sep 2004 → Jun 2007 | acute lung injury | University Hospital, Geneva | Completed | No outcome recorded |
| — | NCT00114478 | Nov 2003 → May 2006 | bronchiolitis | Kern Medical Center | Unknown | No outcome recorded |
| — | NCT00162422 | Aug 2003 → ? | asthma | Hadassah Medical Organization | Unknown | No outcome recorded |
| — | NCT00162487 | Aug 2002 → ? | chronic renal failure syndrome | Hadassah Medical Organization | Unknown | No outcome recorded |
| — | NCT00039988 | Nov 2001 → Mar 2006 | multiple sclerosis | National Institute of Allergy and Infectious Diseases (NIAID) | Completed | No outcome recorded |
| — | NCT00027391 | Sep 2001 → Aug 2004 | muscular dystrophy, scapulohumeral | FDA Office of Orphan Products Development | Completed | No outcome recorded |
| — | NCT00162396 | Aug 1999 → ? | asthma | Hadassah Medical Organization | Unknown | No outcome recorded |
| — | NCT00004685 | Jan 1998 → Sep 2000 | facioscapulohumeral muscular dystrophy | Ohio State University | Completed | No outcome recorded |
| — | NCT00005110 | — | cystic fibrosis | National Center for Research Resources (NCRR) | Suspended | No outcome recorded |
Also used as a comparator or background therapy in 223 trials
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 01 trial | ||||||
| Phase 0 | NCT04901715 Comparator | Jun 2021 → Jul 2024 | primary ciliary dyskinesia | University of North Carolina, Chapel Hill | Completed | No outcome recorded |
| Phase 114 trials | ||||||
| Phase 1 | NCT05366764 Background | Jun 2022 → Feb 2023 | asthma | Sanofi | Completed | No outcome recorded |
| Phase 1 | NCT05035862 Background | Mar → Dec 2022 | asthma | Emory University | Terminated | No outcome recorded |
| Phase 1 | NCT04929626 Comparator | Jan → Nov 2022 | status asthmaticus | Ziauddin University | Completed | No outcome recorded |
| Phase 1 | NCT04848662 Background | May → Jul 2021 | asthma | Bond Avillion 2 Development LP | Completed | No outcome recorded |
| Phase 1 | NCT04488705 Background | Aug 2020 → May 2021 | — | Enterprise Therapeutics Ltd | Completed | No outcome recorded |
| Phase 1 | NCT03934333 Background | May → Sep 2019 | — | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT02401074 Background | Nov 2018 → Jun 2020 | asthma | Lu Yuan Lee | Withdrawn | No outcome recorded |
| Phase 1 | NCT03287310 Background | Oct 2017 → Jul 2019 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 1 | NCT03059017 Comparator | Feb 2017 | lung disorder | British University In Egypt | Completed | No outcome recorded |
| Phase 1 | NCT02872597 Background | Sep 2016 → Aug 2018 | status asthmaticus | University Hospitals Cleveland Medical Center | Completed | No outcome recorded |
| Phase 1 | NCT05006235 Comparator | Feb 2014 → Dec 2015 | persistent tachypnoe of infancy, usual | Ahmed Noaman | Completed | No outcome recorded |
| Phase 1 | NCT00869596 Comparator | Mar → Sep 2009 | lower respiratory tract disorder | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 1 | NCT00673621 Background | May → Nov 2008 | asthma, diabetes mellitus | Mannkind Corporation | Completed | No outcome recorded |
| Phase 1 | NCT00565591 Comparator | Nov 2007 → Jan 2008 | allergic asthma | Respirics Inc. | Completed | No outcome recorded |
| Phase 1/21 trial | ||||||
| Phase 1/2 | NCT04433104 Background | Jun 2020 → Jul 2021 | chronic obstructive pulmonary disease | Vinmec Research Institute of Stem Cell and Gene Technology | Completed | No outcome recorded |
| Phase 239 trials | ||||||
| Phase 2 | NCT06676319 Background | Nov 2024 → Jun 2027 expected | asthma | Sanofi | Active not recruiting | No outcome recorded |
| Phase 2 | NCT06482294 Background | Jun 2024 → May 2025 | asthma | Università degli Studi di Ferrara | Unknown | No outcome recorded |
| Phase 2 | NCT06095258 Comparator | Dec 2023 → Nov 2025 | long COVID-19 | Chinese University of Hong Kong | Unknown | No outcome recorded |
| Phase 2 | NCT05819541 Background | Oct 2023 → Mar 2026 | status asthmaticus | Vanderbilt University Medical Center | Completed | No outcome recorded |
| Phase 2 | NCT05987371 Background | Aug 2023 → Jan 2024 | chronic obstructive pulmonary disease | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Completed | No outcome recorded |
| Phase 2 | NCT05363670 Comparator | Jul 2022 → Feb 2024 | asthma | ARS Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT04589663 Background | Jun 2021 → Apr 2022 | asthma | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT04643158 Background | Mar 2021 → Jul 2023 | asthma | AstraZeneca | Terminated | No outcome recorded |
| Phase 2 | NCT04565847 Comparator | Nov 2020 → Dec 2021 | — | McMaster University | Completed | No outcome recorded |
| Phase 2 | NCT03707678 Background | Jan → Dec 2019 | asthma | GlaxoSmithKline | Withdrawn | No outcome recorded |
| Phase 2 | NCT03345407 Background | Nov 2017 → Jan 2019 | chronic obstructive pulmonary disease | GlaxoSmithKline | Terminated | No outcome recorded |
| Phase 2 | NCT03012061 Background | Jan 2017 → May 2018 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 2 | NCT02794519 Background | Sep → Oct 2016 | asthma | GlaxoSmithKline | Withdrawn | No outcome recorded |
| Phase 2 | NCT02720081 Background | May 2016 → Aug 2017 | asthma | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 2 | NCT02573870 Background | Dec 2015 → Jul 2016 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 2 | NCT02479412 Background | Jun 2015 → Feb 2016 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT02427165 Comparator | Apr → Nov 2015 | asthma | Verona Pharma, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT02299375 Background | Dec 2014 → Jun 2016 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 2 | NCT02271334 Comparator | Aug → Oct 2014 | asthma | Amphastar Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT02210806 Comparator | Jul → Sep 2014 | asthma | Amphastar Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT02108743 Comparator | Jun 2014 → Jul 2016 | idiopathic pulmonary arterial hypertension | American Medical Association Foundation | Withdrawn | No outcome recorded |
| Phase 2 | NCT01899144 Comparator | Jul → Oct 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01854047 Background | Jun 2013 → Nov 2014 | asthma | Sanofi | Completed | No outcome recorded |
| Phase 2 | NCT02162784 Comparator | Feb 2013 → Aug 2014 | asthma | Intech Biopharm Ltd. | Completed | No outcome recorded |
| Phase 2 | NCT01772368 Background | Jan → Jun 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01615874 Background | Jan → Sep 2013 | asthma | Organon and Co | Withdrawn | No outcome recorded |
| Phase 2 | NCT01641692 Background | May 2012 → Feb 2013 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 2 | NCT01576718 Background | Apr 2012 → Jul 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01479621 Background | Jan 2012 → Jul 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01425801 Comparator | Aug 2011 → Feb 2012 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT01312961 Background | Mar 2011 → Oct 2012 | asthma | Sanofi | Completed | No outcome recorded |
| Phase 2 | NCT00677729 Comparator | Nov 2008 → Apr 2009 | bronchiolitis | Queen's University | Completed | No outcome recorded |
| Phase 2 | NCT00632502 Background | May 2008 → Feb 2009 | asthma | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 2 | NCT00545272 Background | Oct 2007 → Apr 2008 | asthma | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT00557466 Background | Oct 2007 → May 2008 | chronic obstructive pulmonary disease | Novartis | Completed | No outcome recorded |
| Phase 2 | NCT00441701 Background | Dec 2006 → Oct 2008 | chronic obstructive pulmonary disease | Merck Sharp & Dohme LLC | Terminated | No outcome recorded |
| Phase 2 | NCT00410150 Background | Apr 2006 → Dec 2007 | status asthmaticus | Children's Hospital Medical Center, Cincinnati | Terminated | No outcome recorded |
| Phase 2 | NCT00117182 Background | Jul 2005 → Aug 2006 | chronic obstructive pulmonary disease | Syntara | Completed | No outcome recorded |
| Phase 2 | NCT00054964 Comparator | Mar → Aug 2003 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 2/33 trials | ||||||
| Phase 2/3 | NCT06657066 Background | Dec 2021 → Apr 2022 | asthma | King Edward Medical University | Completed | No outcome recorded |
| Phase 2/3 | NCT00434993 Comparator | Aug 2007 → Sep 2008 | adult acute respiratory distress syndrome | National Heart, Lung, and Blood Institute (NHLBI) | Terminated | No outcome recorded |
| Phase 2/3 | NCT00633919 Comparator | Jul 2006 → Dec 2008 | allergic disease | ALK-Abelló A/S | Completed | No outcome recorded |
| Phase 360 trials | ||||||
| Phase 3 | NCT05776927 Background | May 2026 → Dec 2028 expected | asthma | Novartis Pharmaceuticals | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT06473779 Background | Sep 2024 → Jun 2027 expected | asthma | AstraZeneca | Active not recruiting | No outcome recorded |
| Phase 3 | NCT06502366 Comparator | Jul 2024 → Mar 2026 overdue | asthma | AstraZeneca | Active not recruiting | No outcome recorded |
| Phase 3 | NCT06429475 Comparator | Jun 2024 → Dec 2028 expected | asthma | University of KwaZulu | Recruiting | No outcome recorded |
| Phase 3 | NCT06261957 Comparator | May 2024 → Sep 2025 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT06052267 Comparator | Aug 2023 → Oct 2026 expected | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Active not recruiting | No outcome recorded |
| Phase 3 | NCT05884970 Comparator | Mar 2023 → Mar 2024 | childhood onset asthma | Canisius-Wilhelmina Hospital | Unknown | No outcome recorded |
| Phase 3 | NCT05555290 Background | Sep 2022 → Nov 2024 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT05527704 Comparator | Dec 2021 → Nov 2025 overdue | pulmonary hypertension, neonatal, respiratory failure | Medical University of Warsaw | Active not recruiting | No outcome recorded |
| Phase 3 | NCT04446637 Comparator | Sep 2021 → Sep 2022 | chronic obstructive pulmonary disease | Neutec Ar-Ge San ve Tic A.Ş | Withdrawn | No outcome recorded |
| Phase 3 | NCT03847896 Comparator | Mar 2019 → Jul 2021 | asthma | Bond Avillion 2 Development LP | Completed | No outcome recorded |
| Phase 3 | NCT03376932 Background | Jan 2019 → Feb 2021 | asthma | GlaxoSmithKline | Withdrawn | No outcome recorded |
| Phase 3 | NCT03769090 Comparator | Dec 2018 → Aug 2021 | asthma | Bond Avillion 2 Development LP | Completed | No outcome recorded |
| Phase 3 | NCT03562195 Background | Aug 2018 → Sep 2022 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT03745261 Background | Jun 2018 → Dec 2019 | chronic obstructive pulmonary disease | Henan University of Traditional Chinese Medicine | Unknown | No outcome recorded |
| Phase 3 | NCT03468790 Background | May 2018 → Jan 2021 | allergic asthma | Shanghai Biomabs Pharmaceutical Co., Ltd. | Completed | No outcome recorded |
| Phase 3 | NCT03549897 Comparator | Mar → Aug 2018 | asthma | Amneal Ireland Limited | Unknown | No outcome recorded |
| Phase 3 | NCT03137303 Background | Jul 2017 → Sep 2019 | — | University of Illinois at Chicago | Completed | No outcome recorded |
| Phase 3 | NCT03184987 Background | Jun 2017 → Jun 2019 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02924688 Background | Oct 2016 → Feb 2019 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02729051 Background | Jun 2016 → May 2017 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02731846 Background | Jun → Nov 2016 | chronic obstructive pulmonary disease | GlaxoSmithKline | Withdrawn | No outcome recorded |
| Phase 3 | NCT02741271 Background | May 2016 → Dec 2017 | asthma | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT02528214 Background | Oct 2015 → Sep 2017 | asthma | Sanofi | Completed | No outcome recorded |
| Phase 3 | NCT02483975 Background | Oct 2015 → Jun 2016 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02513160 Background | Sep 2015 → Mar 2016 | chronic asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02502734 Background | Sep → Dec 2015 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02478398 Background | Jul 2015 → Nov 2018 | seasonal allergic rhinitis | Merck Sharp & Dohme LLC | Completed | No outcome recorded |
| Phase 3 | NCT02477397 Comparator | May 2015 → Jun 2019 | chronic obstructive pulmonary disease | University Medical Center Groningen | Unknown | No outcome recorded |
| Phase 3 | NCT02414854 Background | Apr 2015 → Jul 2017 | asthma | Sanofi | Completed | No outcome recorded |
| Phase 3 | NCT02127697 Background | Mar 2015 → May 2017 | asthma | Novartis Pharmaceuticals | Withdrawn | No outcome recorded |
| Phase 3 | NCT02345161 Background | Jan 2015 → Apr 2016 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02257385 Background | Oct 2014 → May 2015 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT02175771 Background | Jul 2014 → Jul 2015 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02139644 Background | Jun 2014 → Sep 2015 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02141854 Background | Jun 2014 → Sep 2015 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02040779 Background | Dec 2013 → Dec 2014 | chronic asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02031640 Background | Dec 2013 → Nov 2014 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT02040766 Background | Dec 2013 → Feb 2016 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 3 | NCT01987219 Comparator | Mar 2013 → Dec 2014 | Riley-Day syndrome | NYU Langone Health | Completed | No outcome recorded |
| Phase 3 | NCT01687296 Background | Nov 2012 → Jun 2013 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT01706328 Background | Oct 2012 → Jun 2013 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT01613326 Background | Jun 2012 → Jan 2013 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01490125 Background | Oct 2011 → Aug 2012 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01431950 Background | Sep 2011 → Oct 2012 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT01323621 Background | Mar 2011 → Jan 2012 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT01313494 Background | Mar 2011 → May 2012 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT01120691 Background | Apr 2010 → Jul 2012 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT01019694 Comparator | Nov 2009 → Apr 2011 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 3 | NCT00861926 Comparator | Mar 2009 → Dec 2010 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 3 | NCT00550550 Background | Nov 2007 → Sep 2009 | allergic rhinitis, conjunctivitis | ALK-Abelló A/S | Completed | No outcome recorded |
| Phase 3 | NCT00562159 Background | Nov 2007 → Sep 2009 | allergic disease, conjunctivitis, rhinitis | ALK-Abelló A/S | Completed | No outcome recorded |
| Phase 3 | NCT00588406 Background | Sep 2007 → Dec 2009 | asthma | Northwell Health | Completed | No outcome recorded |
| Phase 3 | NCT00394329 Background | Nov 2006 → Dec 2011 | asthma | Milton S. Hershey Medical Center | Completed | No outcome recorded |
| Phase 3 | NCT00384189 Comparator | Sep 2006 → Aug 2007 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00497523 Comparator | Mar 2006 → Jan 2007 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 3 | NCT00628758 Background | Dec 2005 → Sep 2008 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00646620 Comparator | Apr → Sep 2003 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00646009 Comparator | Mar → Aug 2003 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT00685126 Comparator | Feb 2001 → Jul 2002 | reactive airway disease | Sumitomo Pharma America, Inc. | Completed | No outcome recorded |
| Phase 460 trials | ||||||
| Phase 4 | NCT07052942 Comparator | Aug 2025 → Nov 2029 expected | acute asthma | DARTNet Institute | Recruiting | No outcome recorded |
| Phase 4 | NCT06816342 Comparator | Nov 2024 → Feb 2025 overdue | asthma | Beni-Suef University | Recruiting | No outcome recorded |
| Phase 4 | NCT07633223 Comparator | Sep 2024 → Aug 2025 | asthma | Beni-Suef University | Completed | No outcome recorded |
| Phase 4 | NCT06152653 Background | Apr 2024 → Apr 2027 expected | asthma, chronic obstructive pulmonary disease | University of California, San Francisco | Recruiting | No outcome recorded |
| Phase 4 | NCT06272370 Comparator | Feb → Sep 2024 | asthma, hypersensitivity reaction disease, obstructive lung disease, respiratory tract infectious disorder | DARTNet Institute | Completed | No outcome recorded |
| Phase 4 | NCT05977699 Comparator | Jan → Nov 2024 | asthma | University of Saskatchewan | Completed | No outcome recorded |
| Phase 4 | NCT06918418 Comparator | Jan → Jun 2024 | acute asthma | Children's Hospital and Institute of Child Health, Multan | Completed | No outcome recorded |
| Phase 4 | NCT05667727 Comparator | Oct 2023 → Jun 2025 | childhood onset asthma | Oman Medical Speciality Board | Completed | No outcome recorded |
| Phase 4 | NCT06036823 Comparator | Oct 2023 → Sep 2025 | mineral metabolism disease | Oman Medical Speciality Board | Completed | No outcome recorded |
| Phase 4 | NCT05173584 Comparator | Nov → Dec 2021 | — | University of Aleppo | Unknown | No outcome recorded |
| Phase 4 | NCT04584034 Comparator | Sep 2021 → Apr 2023 | — | UMC Utrecht | Withdrawn | No outcome recorded |
| Phase 4 | NCT04276233 Background | Jun 2021 → Oct 2023 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT04655170 Comparator | Dec 2020 → Jan 2023 overdue | chronic obstructive pulmonary disease | University of Tennessee Graduate School of Medicine | Recruiting | No outcome recorded |
| Phase 4 | NCT04159519 Background | Jul 2020 → Jan 2023 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT03880903 Background | Jul 2020 → Mar 2021 | acute bronchiolitis | Assiut University | Unknown | No outcome recorded |
| Phase 4 | NCT03952286 Background | Aug 2019 → Dec 2020 | childhood onset asthma | University of Arizona | Completed | No outcome recorded |
| Phase 4 | NCT03822637 Background | Feb 2019 → Feb 2025 | asthma | University of California, San Francisco | Terminated | No outcome recorded |
| Phase 4 | NCT04750603 Comparator | Dec 2018 → Jan 2020 | childhood onset asthma | Rambam Health Care Campus | Completed | No outcome recorded |
| Phase 4 | NCT03478683 Background | Jun 2018 → Mar 2019 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT03478696 Background | Jun 2018 → Mar 2019 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT03474081 Background | Mar 2018 → Jul 2019 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT03363191 Background | Mar 2018 → May 2019 | asthma | GlaxoSmithKline | Withdrawn | No outcome recorded |
| Phase 4 | NCT03380429 Background | Jan 2018 → Jan 2019 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT03405090 Comparator | Sep 2017 → Mar 2022 | chronic obstructive pulmonary disease | Dr. Denis O'Donnell | Completed | No outcome recorded |
| Phase 4 | NCT02889809 Background | Jul 2017 → Apr 2021 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT03333395 Comparator | Feb → Sep 2017 | — | Ain Shams University | Completed | No outcome recorded |
| Phase 4 | NCT02799784 Background | Jul 2016 → Apr 2017 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT02508311 Comparator | Jun 2016 → Mar 2022 | myopathy, spinal cord injury | VA Office of Research and Development | Terminated | No outcome recorded |
| Phase 4 | NCT02319564 Comparator | Apr → Oct 2016 | — | University of Calgary | Withdrawn | No outcome recorded |
| Phase 4 | NCT02654145 Background | Mar 2016 → May 2017 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT02584738 Background | Sep 2015 → Jan 2016 | asthma | Hospital General Naval de Alta Especialidad - Escuela Medico Naval | Unknown | No outcome recorded |
| Phase 4 | NCT02371629 Background | Jun 2015 → Nov 2016 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT02275052 Background | Jan 2015 → Jun 2016 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT02233803 Background | Nov 2014 → Dec 2015 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT02257372 Background | Sep 2014 → Mar 2015 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT01997463 Background | Aug 2014 → Jun 2016 | childhood onset asthma | University of Arizona | Completed | No outcome recorded |
| Phase 4 | NCT01978418 Comparator | Nov 2013 → Sep 2015 | lung disorder | Sture Andersson | Unknown | No outcome recorded |
| Phase 4 | NCT01951378 Comparator | Sep 2013 → Jun 2016 | asthma | Seton Healthcare Family | Terminated | No outcome recorded |
| Phase 4 | NCT01907334 Comparator | Aug 2013 → May 2014 | asthma | University of Florida | Completed | No outcome recorded |
| Phase 4 | NCT01922271 Background | Aug 2013 → Jan 2014 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT01691482 Comparator | Jul → Oct 2012 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT01471340 Background | Jan 2012 → Nov 2016 | asthma | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT01515995 Background | Jan 2012 → Oct 2015 | asthma | University of Texas Southwestern Medical Center | Completed | No outcome recorded |
| Phase 4 | NCT01338311 Comparator | Mar 2011 → Mar 2012 | asthma | University of Saskatchewan | Completed | No outcome recorded |
| Phase 4 | NCT00831376 Comparator | Jan 2009 → Apr 2012 | asthma | University of Dundee | Completed | No outcome recorded |
| Phase 4 | NCT00830882 Comparator | Jan 2009 → Jan 2010 | asthma | University of Dundee | Withdrawn | No outcome recorded |
| Phase 4 | NCT00900874 Comparator | Jan 2009 → May 2010 | asthma | All India Institute of Medical Sciences | Unknown | No outcome recorded |
| Phase 4 | NCT01151579 Comparator | Dec 2008 → Nov 2009 | chronic obstructive pulmonary disease, infectious disease with sepsis | Fahim Khorfan, MD | Completed | No outcome recorded |
| Phase 4 | NCT00911651 Comparator | Jun → Jul 2008 | chronic obstructive pulmonary disease | University Hospital, Antwerp | Completed | No outcome recorded |
| Phase 4 | NCT00567476 Comparator | Nov 2007 → Apr 2010 | asthma | Novartis | Completed | No outcome recorded |
| Phase 4 | NCT00487773 Comparator | Sep 2007 → Sep 2008 | asthma | Medical University of Lodz | Completed | No outcome recorded |
| Phase 4 | NCT00530062 Comparator | Jul 2007 → Oct 2008 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | No outcome recorded |
| Phase 4 | NCT00393367 Background | Dec 2006 → Nov 2007 | acute asthma, reactive airway disease | Children's Hospital of Philadelphia | Completed | No outcome recorded |
| Phase 4 | NCT00363480 Background | May 2006 → Sep 2007 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT01091337 Comparator | May 2006 → Sep 2009 | asthma | Otsuka Pharmaceutical Co., Ltd. | Completed | No outcome recorded |
| Phase 4 | NCT00315744 Background | Nov 2004 → Apr 2007 | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT00600639 Background | Jan 2004 → Dec 2007 | acute respiratory failure | IRCCS Azienda Ospedaliero-Universitaria di Bologna | Terminated | No outcome recorded |
| Phase 4 | NCT00070707 Background | Apr → Nov 2003 | asthma, seasonal allergic rhinitis | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT00667797 Comparator | Mar 2003 → May 2005 | asthma, chronic obstructive pulmonary disease | Sumitomo Pharma America, Inc. | Completed | No outcome recorded |
| Phase 4 | NCT00189436 Comparator | Mar 2003 → Jan 2009 | asthma | Deborah Gentile | Completed | No outcome recorded |
| Phase not applicable45 trials | ||||||
| — | NCT07350421 Comparator | Jan 2026 → Jan 2027 expected | — | Latakia University | Not yet recruiting | No outcome recorded |
| — | NCT07037511 Comparator | Oct 2025 → Dec 2029 expected | asthma | University of British Columbia | Recruiting | No outcome recorded |
| — | NCT06609941 Background | Jun 2024 → Jan 2025 overdue | asthma | Foundation University Islamabad | Recruiting | No outcome recorded |
| — | NCT05550402 Comparator | Feb → Jun 2024 | asthma, obstructive lung disease, parasympathetic nervous system disorder | Hat Yai Medical Education Center | Unknown | No outcome recorded |
| — | NCT05724745 Background | May 2023 → May 2028 expected | asthma, chronic obstructive pulmonary disease | French Alternative Energies and Atomic Energy Commission | Recruiting | No outcome recorded |
| — | NCT05930847 Background | Feb → Apr 2022 | childhood onset asthma | Ege University | Completed | No outcome recorded |
| — | NCT05099107 Comparator | Oct 2021 → Mar 2025 | centronuclear myopathy, nemaline myopathy, neuromuscular disease | Vastra Gotaland Region | Completed | No outcome recorded |
| — | NCT02509299 Background | Sep → Nov 2019 | chronic obstructive pulmonary disease | University of Granada | Completed | No outcome recorded |
| — | NCT03902106 Comparator | Mar 2019 → Jun 2021 | — | University of Copenhagen | Unknown | No outcome recorded |
| — | NCT03620422 Comparator | Jan 2019 → Jan 2020 | asthma | McMaster University | Completed | No outcome recorded |
| — | NCT03814954 Comparator | Jan 2019 → Aug 2021 | — | Makassed General Hospital | Completed | No outcome recorded |
| — | NCT03842839 Background | Oct 2018 → Dec 2022 | — | Guangzhou Institute of Respiratory Disease | Unknown | No outcome recorded |
| — | NCT03556683 Background | Oct 2018 → Jun 2024 | asthma | University of North Carolina, Chapel Hill | Completed | No outcome recorded |
| — | NCT03296579 Background | Jun → Nov 2018 | acute asthma, childhood onset asthma | University of British Columbia | Unknown | No outcome recorded |
| — | NCT03522831 Comparator | May 2018 → Dec 2027 expected | cystic fibrosis, lung disorder | University of British Columbia | Active not recruiting | No outcome recorded |
| — | NCT03430505 Comparator | Jun 2017 → Jul 2018 | asthma | University of Nove de Julho | Completed | No outcome recorded |
| — | NCT02790047 Background | Oct 2016 → Jan 2018 | chronic obstructive pulmonary disease | Khon Kaen University | Unknown | No outcome recorded |
| — | NCT02766673 Comparator | Aug 2016 → Jun 2018 | bronchopulmonary dysplasia | Children's Hospital of Philadelphia | Completed | No outcome recorded |
| — | NCT02686086 Comparator | Feb 2016 → Jul 2017 | chronic obstructive pulmonary disease | Beaumont Hospital | Completed | No outcome recorded |
| — | NCT02499887 Background | Jan → Sep 2016 | asthma, chronic obstructive pulmonary disease | State University of New York at Buffalo | Terminated | No outcome recorded |
| — | NCT02566902 Background | Oct 2015 → Jun 2017 | asthma | Seton Healthcare Family | Completed | No outcome recorded |
| — | NCT02523833 Background | Sep 2015 → Jun 2017 | hypersensitivity pneumonitis | University of Sao Paulo General Hospital | Completed | No outcome recorded |
| — | NCT02515318 Comparator | Sep 2015 → Mar 2017 | chronic obstructive pulmonary disease | University of Granada | Unknown | No outcome recorded |
| — | NCT02458482 Comparator | Jul 2015 → Nov 2020 | asthma | Vanderbilt University Medical Center | Withdrawn | No outcome recorded |
| — | NCT02252302 Comparator | May 2015 → Aug 2016 | exercise-induced bronchoconstriction | University of British Columbia | Completed | No outcome recorded |
| — | NCT02073747 Comparator | Apr → Jul 2015 | asthma | University Medical Center of Southern Nevada | Completed | No outcome recorded |
| — | NCT02159196 Comparator | Jul 2014 → Mar 2017 | respiratory failure | Academic Medical Center - University of Amsterdam | Completed | No outcome recorded |
| — | NCT02341573 Comparator | Mar 2013 → Jun 2015 | childhood onset asthma | Children's Hospital of Fudan University | Completed | No outcome recorded |
| — | NCT01714401 Comparator | Mar 2012 → May 2013 | — | Medical University of Gdansk | Completed | No outcome recorded |
| — | NCT02453750 Background | Feb 2012 → Oct 2013 | congenital diaphragmatic hernia | The Hospital for Sick Children | Completed | No outcome recorded |
| — | NCT02069665 Comparator | Dec 2011 → Jul 2013 | pneumonia | Liaoning University of Traditional Chinese Medicine | Completed | No outcome recorded |
| — | NCT01856959 Comparator | Nov 2011 → Mar 2013 | asthma | Chongqing Medical University | Completed | No outcome recorded |
| — | NCT01447069 Comparator | Oct 2011 → Mar 2012 | cardiomyopathy, heart failure | Rabin Medical Center | Unknown | No outcome recorded |
| — | NCT01415596 Comparator | Aug 2011 → Aug 2012 | — | Bispebjerg Hospital | Unknown | No outcome recorded |
| — | NCT01187589 Background | Dec 2010 → Sep 2011 | chronic obstructive pulmonary disease | Respinova LTD | Completed | No outcome recorded |
| — | NCT01238848 Background | Dec 2010 → Oct 2011 | acute bronchiolitis | Hospital General de Niños Pedro de Elizalde | Completed | No outcome recorded |
| — | NCT00981851 Comparator | Sep 2009 → May 2011 | cardiovascular disorder, chronic obstructive pulmonary disease | Radboud University Medical Center | Completed | No outcome recorded |
| — | NCT01073527 Comparator | Jan 2009 → Jul 2011 | asthma | Wolfson Medical Center | Completed | No outcome recorded |
| — | NCT00876135 Comparator | Dec 2008 → May 2013 | asthma | Laval University | Completed | No outcome recorded |
| — | NCT00608790 Background | Feb 2008 → Dec 2012 | tuberculosis | University of Cape Town | Unknown | No outcome recorded |
| — | NCT00521222 Background | Jun 2007 → Nov 2010 | asthma | Columbia University | Completed | No outcome recorded |
| — | NCT00388739 Background | Nov 2006 | asthma | Baylor College of Medicine | Withdrawn | No outcome recorded |
| — | NCT00180843 Comparator | Sep 2005 → Feb 2008 | chronic obstructive pulmonary disease | Imperial College London | Terminated | No outcome recorded |
| — | NCT01143688 Comparator | Jan 2005 → Jan 2009 | — | Brigham and Women's Hospital | Completed | No outcome recorded |
| — | NCT00319488 Comparator | Feb 2004 → Nov 2006 | asthma, lung disorder | National Heart, Lung, and Blood Institute (NHLBI) | Completed | No outcome recorded |
Press releases naming this drug 13 releases
| Date | Issuer | Release |
|---|---|---|
| 2022-09-07 | Teva Branded Pharmaceutical Products R&D, Inc. | CONNECT1 Study Published in Journal of Allergy and Clinical Immunology: In Practice Evaluates the Potential of ProAir® Digihaler® (albuterol sulfate) Inhalation Powder and Digihaler System to Help Improve Asthma Management tevapharm.com ↗ |
| 2022-08-29 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva to Present First Data Set from the CONNECT1 Clinical Trial on ProAir® Digihaler® (albuterol sulfate) Inhalation Powder at the European Respiratory Society (ERS) International Congress 2022 tevapharm.com ↗ |
| 2022-05-17 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces New Findings Highlighting Potential of ProAir® Digihaler® (albuterol sulfate) Inhalation Powder to Address Asthma Treatment Challenges tevapharm.com ↗ |
| 2022-05-12 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva to Present Findings on Short-Acting Beta Agonist (SABA) Use in Asthma Patients and the Potential of ProAir® Digihaler® (albuterol sulfate) Inhalation Powder to Help Inform Treatment Decisions at American Thoracic Society 2022 Annual Meeting tevapharm.com ↗ |
| 2020-07-13 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces Availability of ProAir® Digihaler® (albuterol sulfate 117 mcg) Inhalation Powder for Patients with Asthma and COPD tevapharm.com ↗ |
| 2018-12-21 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces FDA Approval of First and Only Digital Inhaler with Built-In Sensors – ProAir® Digihaler™ (albuterol sulfate 117 mcg) Inhalation Powder tevapharm.com ↗ |
| 2016-04-29 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces FDA Approval of ProAir RespiClick® (albuterol sulfate) Inhalation Powder for Pediatric Asthma Patients Ages 4 to 11 tevapharm.com ↗ |
| 2015-09-10 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces FDA Acceptance of a Supplemental New Drug Application for ProAir® RespiClick (albuterol sulfate) Inhalation Powder for Pediatric Patients tevapharm.com ↗ |
| 2014-11-07 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Presents Data for Investigational Short-Acting Beta-Agonist Inhaler (Albuterol MDPI) at 2014 Annual Scientific Meeting of the American College of Allergy, Asthma & Immunology tevapharm.com ↗ |
| 2014-07-14 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva Announces FDA Acceptance of NDA Filing for Investigational Short-Acting Beta-Agonist (SABA) Inhaler (Albuterol MDPI) tevapharm.com ↗ |
| 2014-06-20 | Otsuka Pharmaceutical Development & Commercialization, Inc. | Meptin, a Fast-acting Bronchodilator to Treat Asthma and COPD, Will Become Available in Japan on July 2 in a New Form as Meptin Swinghaler 10μg 100Puffs®®® otsuka.co.jp ↗ |
| 2014-02-17 | Otsuka Pharmaceutical Development & Commercialization, Inc. | Meptin Swinghaler, Easy-to-inhale Bronchodilator for COPD and Asthma Patients, Approved in Japan otsuka.co.jp ↗ |
| 2008-09-24 | Teva Branded Pharmaceutical Products R&D, Inc. | Teva's Proair® HFA, the Market Leading Albuterol Inhaler, Receives New Pediatric Indication tevapharm.com ↗ |
Evidence & citations 58 cited values
Every value below carries the sentence it was read from. 433 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | salbutamol | “A short-acting β2-adrenergic agonists (SABA), albuterol/salbutamol hydrofluoroalkane (HFA) metered dose inhaler (MDI), was provided to be used as needed for the relief of...” NCT01479621 ↗229“A short-acting β2-adrenergic agonists (SABA), albuterol/salbutamol hydrofluoroalkane (HFA) metered dose inhaler (MDI), was provided to be used as needed for the relief of...” NCT01576718 ↗ “A short-acting β2-adrenergic agonists (SABA), albuterol/salbutamol hydrofluoroalkane (HFA) metered dose inhaler (MDI), was provided to be used as needed for the relief of...” NCT02139644 ↗ “Each patient's current rescue medication was replaced with study-supplied albuterol/salbutamol hydrofluoroalkane (HFA) metered-dose inhaler (MDI) (90 mcg ex-actuator) or...” NCT02513160 ↗ “A Study Designed to Determine if the Drugs Albuterol (Salbutamol) and Fluticasone Have an Effect on the Pharmacokinetics of the Investigational Product Technosphere® Insulin...” NCT00674050 ↗ “Rescue medication (albuterol/salbutamol hydrofluoroalkane (HFA) MDI [90 mcg ex-actuator] or equivalent) for use on an as-needed basis for the immediate relief of asthma...” NCT02040766 ↗ “Rescue medication (albuterol/salbutamol hydrofluoroalkane (HFA) MDI [90 mcg ex-actuator] or equivalent) for use on an as-needed basis for the immediate relief of asthma...” NCT02040779 ↗ “Salbutamol Sulphate Inhalation Aerosol (Ventolin®, GlaxoSmithKline Australia Pty Ltd.), 100 μg/press, 200 press, 100 μg each time (when needed), no more than 8 press daily for 12 weeks.” NCT03169504 ↗ “In addition to study intervention, all participants will be provided with a SABA as rescue medication (eg, salbutamol/albuterol), to be used throughout the Run-in and Treatment Periods.” NCT04643158 ↗ “Three concentrations of topical salbutamol gel will be compared, in a group-wise fashion, with a placebo administration at one incision site on each arm of the trial subjects.” NCT03514615 ↗ “Albuterol/salbutamol will be available as an inhalation via metered-dose inhaler (MDI) with a spacer and will be issued for reversibility testing at Visit 1” NCT02345161 ↗ “The salbutamol collected on the filter was extracted with 90% acetonitrile and sonicated for 3 minutes, a process validated to recover the full drug dose.” NCT06816342 ↗ “Albuterol/salbutamol will be provided as an inhalation via MDI with a spacer or nebules and will be given as a rescue medication throughout the study.” NCT03474081 ↗ “A bronchodilator (Salbutamol 200 mcg or 2 puffs inhaled via spacer device) will be administered to all subjects in the pulmonary function laboratory.” NCT02453750 ↗ “Albuterol/salbutamol HFA metered dose inhaler (MDI) was supplied to participants throughout the study to be used as needed as a rescue medication.” NCT02175771 ↗ “Participant choice of short-acting beta-2 agonist (salbutamol/albuterol), anticholinergic, or combination medication as needed for asthma symptoms” NCT00632502 ↗ “One year Diskus® fluticasone/salmeterol 500/50 μg one inhalation twice daily + salbutamol 100 μg as needed with a maximum of 8 inhalations daily.” NCT02477397 ↗ “Albuterol/salbutamol will be supplied as an inhalation spray via metered dose inhaler and will be issued for reversibility testing at Visit 1.” NCT02799784 ↗ “All subjects will be provided albuterol/salbutamol inhalation aerosol, to use as needed to treat acute asthma symptoms throughout the study.” NCT02483975 ↗ “Albuterol/salbutamol will be administered via metered-dose inhaler (MDI) with a spacer as needed throughout the study as a rescue medication” NCT02731846 ↗ “Albuterol/salbutamol MDI (metered-dose inhaler) or nebules will be permitted throughout the study as rescue medication, for use as-needed.” NCT02275052 ↗ “Subjects will be provided short-acting albuterol/salbutamol as-rescue medication to be used on an as-needed basis throughout the study.” NCT03478683 ↗ “Rescue medication (albuterol/salbutamol) was dispensed at each visit, if needed, as determined by the investigational center personnel.” NCT02141854 ↗ “Rescue medication (salbutamol/albuterol) shall be supplied to subjects at Screening for use when needed during the study.” NCT02794519 ↗ “PT027 is a fixed-dose combination of albuterol (salbutamol) and budesonide in a single pressurized metered-dose inhaler.” PMID 34699967 ↗ Oct 2021 “Albuterol/salbutamol is to be administered via metered-dose inhaler as a rescue drug on need basis throughout the study.” NCT03012061 ↗ “Home use of nebulized Β2-agonist such as salbutamol 5 mg or terbutaline 10 mg for symptoms of intercurrent bronchospasm.” NCT00567476 ↗ “Any therapy that is prescribed as per asthma guidelines i.e. beclomethasone, budesonide and salbutamol, montelukast etc” NCT06429475 ↗ “Test of Bronchodilatation (combined Salbutamol 200μg and Ipratropium bromure 80μg; 2 inhalations): wait 30 min and then” NCT03062904 ↗ “Albuterol/salbutamol metered dose inhalers (MDIs) will be provided as rescue medication during treatment period.” NCT02654145 ↗ “Subjects will also receive albuterol/salbutamol as a rescue medication when needed during the treatment period.” NCT02729051 ↗ “Salbutamol/albuterol - 2 puffs of salbutamol/albuterol approximately every 4 hours as needed for dyspnea relief” NCT00441701 ↗ “Asthma therapy: budesonide and salbutamol being the most frequently used (excluding MF and indacaterol acetate)” NCT04589663 ↗ “100 μg / 90 μg salbutamol/albuterol Metered Dose Inhaler (MDI) or equivalent dose of Dry Powder Inhaler (DPI).” NCT00557466 ↗ “100 μg/ 90 μg salbutamol/albuterol Metered Dose Inhaler (MDI) or equivalent dose of Dry Powder Inhaler (DPI).” NCT00545272 ↗ “Albuterol/Salbutamol MDI will be administered for symptom relief from screening to the end of the study.” NCT03707678 ↗ “In addition, all subjects will be provided with albuterol/salbutamol for relief of asthma symptoms.” NCT01431950 ↗ “Albuterol (Salbutamol) MDI or nebules will be provided to all subjects as a rescue medication.” NCT03345407 ↗ “albuterol MDI 90 mcg OR or salbutamol HFA MDI 100 mcg for rescue medication, taken as directed” NCT01615874 ↗ “Albuterol/salbutamol MDI or nebules for as needed use will be issued throughout the study.” NCT02257385 ↗ “Salbutamol(200µg), Salmeterol (50µg) and Fluticasone propionate (500µg) by inhalation” NCT03524066 ↗ “Salbutamol/albuterol was available for rescue medication use throughout the study.” NCT01120691 ↗ “0.5 mg ipratropium bromide + 2.5 mg salbutamol will be inhaled via nebulizer” NCT03405090 ↗ “Albuterol/salbutamol will be supplied as inhalation aerosol or nebulizer.” NCT02889809 ↗ “Albuterol/salbutamol will be delivered as a rescue medication via MDI.” NCT03376932 ↗ “Short acting inhaled β2 agonists ( salbutamol and terbutaline)” NCT02515318 ↗ “Short acting inhaled β2 agonists ( salbutamol and terbutaline)” NCT02509299 ↗ “Albuterol (salbutamol) is a widely used asthma medication” NCT00385359 ↗ “400 mcg salbutamol administered per metered dose inhaler” NCT04914273 ↗ “of Salbutamol Sulfate, 288 mcg of Ipratropium Bromide” NCT02173678 ↗ “Albuterol/Salbutamol 90 mcg - 100 mcg per inhalation” NCT02720081 ↗ “Combivent®, ipratropium 0.5 mg + salbutamol 2.5 mg” NCT00354354 ↗ “Salbutamol inhaler (Short acting bronchodilator)” NCT06609941 ↗ “Albuterol/salbutamol Metered Dose Inhaler (MDI)” NCT02257372 ↗ “Ventolin® MDI * Ingredient: Salbutamol sulfate” NCT01076322 ↗ “Albuterol 90 mcg /salbutamol 100 mcg HFA MDI” NCT01471340 ↗ “Salbutamol 100μg / Albuterol 90μg” NCT05776927 ↗ “Salbutamol(Albuterol) Sulfate” NCT03098680 ↗ “Albuterol/salbutamol (daily)” NCT01691482 ↗ “Salbutamol 200 µg/dose dmDPI” NCT05084222 ↗ “Salbutamol (oral or inhaler)” NCT02790047 ↗ “Drug: Albuterol/Salbutamol” NCT02414854 ↗ “Albuterol/Salbutamol PRN” NCT02741271 ↗ “Salbutamol, Terbutaline” NCT04433104 ↗ “albuterol (salbutamol)” NCT00114478 ↗ “salbutamol inhalation” NCT03208894 ↗ “Albuterol/salbutamol” NCT02924688 ↗ “albuterol/salbutamol” NCT03478696 ↗ “Albuterol/salbutamol” NCT02031640 ↗ “Albuterol/Salbutamol” NCT02528214 ↗ |
| Known as | A004 | “This 12-week clinical study evaluates the safety and efficacy of Albuterol Sulfate HFA Inhalation Aerosol (Albuterol-HFA, or: A004), Armstrong's proposed HFA formulation of...” NCT00635505 ↗ |
| Known as | A006 | “A006 (Albuterol Dry Powder Inhaler (DPI)), in comparison with those of an active control, Proventil-HFA (Albuterol Metered Dose Inhaler (MDI))” NCT01189396 ↗3“A006 albuterol inhalation powder, 120 mcg/inhalation, one inhalation” NCT01174732 ↗ “A006, an Albuterol dry powder inhaler (DPI)” NCT01581177 ↗ |
| Known as | ABS | “This is a Phase 3B, 12-week, multicenter, open-label study to evaluate the relationship between albuterol sulfate (ABS) eMDPI and clinical asthma exacerbation (CAE) in adult...” NCT02969408 ↗2“Albuterol sulfate (ABS) dry powder inhaler with an integrated electronic module (eMDPI)” NCT06664619 ↗ “fluticasone propionate (Fp) and albuterol sulfate (ABS), delivered in combination” NCT06290102 ↗ |
| Known as | aerolin nebulis | “Nebulized bronchodilator drugs will be Salbutamol Sulfate (aerolin nebulis) and ipratropium bromide (atrovent) diluted in a saline solution (saline 0.9%) in 3 ml.” NCT03271905 ↗ |
| Known as | ALB | “comparing the fixed combination of ipratropium and albuterol (IB+ALB) to albuterol alone (ALB).” PMID 18403223 ↗ Mar 2008 |
| Known as | ALB-HFA | “albuterol hydrofluoroalkaline (ALB-HFA) alone after 4 weeks” PMID 27130202 ↗ Apr 2016 |
| Known as | albuterol | “BACKGROUND: Treatment guidelines recommend the regular use of inhaled corticosteroids for patients with mild persistent asthma. We investigated whether the symptom-driven use...” PMID 17507703 ↗ May 2007211“Participants were randomly assigned in a 1:1 ratio to a fixed-dose combination of 180 μg of albuterol and 160 μg of budesonide (with each dose consisting of two inhaler...” PMID 40388330 ↗ May 2025 “participants will use either a combination of budesonide/formoterol or mometasone/formoterol as both controller and rescue therapy or a stand alone inhaled steroid...” NCT06272370 ↗ “This study evaluates the efficacy, dose-ranging and safety profiles of A006, an Albuterol dry powder inhaler (DPI), in the dose range of 110 to 220 mcg per dose in comparison...” NCT02210806 ↗ “The aim is to asses that using Nebulized Hypertonic Saline with bronchodilators (albuterol) may reduce the days of hospitalization and improve clinical outcomes in patients...” NCT01238848 ↗ “The effects of albuterol delivered via AS MDI and Proventil on bronchodilation were equivalent, supporting the selection of AS MDI 180 µg to be taken into Phase III clinical...” PMID 34089147 ↗ Jun 2021 “The purpose of the project is to investigate whether the use of a WADA approved dose of salbutamol (albuterol/Ventoline) has a performance-enhancing effect on sprint...” NCT04402658 ↗ “All subjects received fluticasone furoate/vilanterol ELLIPTA dry-powder inhalers for maintenance and salbutamol/albuterol metered-dose inhalers for rescue, with a sensor...” PMID 33334936 ↗ Jun 2021 “In addition to study intervention, all participants will be provided with a SABA as rescue medication (eg, salbutamol/albuterol), to be used throughout the Run-in and Treatment Periods.” NCT04643158 ↗ “FDA approval of Airsupra (with both albuterol and budesonide in one inhaler) provides a unique opportunity to introduce ICS (along with albuterol) to ED patients with acute asthma.” NCT07166939 ↗ “Salbutamol/Albuterol, short-activing beta agonist provided to all subjects to be taken as needed for the relief of asthma symptoms.throughout the study period” NCT01641692 ↗ “Participant choice of short-acting beta-2 agonist (salbutamol/albuterol), anticholinergic, or combination medication as needed for asthma symptoms” NCT00632502 ↗ “Combination Product: Budesonide/albuterol sulfate metered-dose inhaler 80/90 μg per puff. Two puffs to administer 160/180 μg dose.” NCT04848662 ↗ “Rescue medication (salbutamol/albuterol) shall be supplied to subjects at Screening for use when needed during the study.” NCT02794519 ↗ “Patients with moderate to severe COPD were randomized to ipratropium bromide/albuterol (20/100mcg) Respimat inhaler” PMID 20172704 ↗ Feb 2010 “Salbutamol/albuterol - 2 puffs of salbutamol/albuterol approximately every 4 hours as needed for dyspnea relief” NCT00441701 ↗ “salbutamol/albuterol (containing CFC-free propellant -HFA 134a) inhaler used as rescue medication when needed.” NCT01490125 ↗ “100 μg / 90 μg salbutamol/albuterol Metered Dose Inhaler (MDI) or equivalent dose of Dry Powder Inhaler (DPI).” NCT00557466 ↗ “When administered PT007, participants will receive 2 actuations of albuterol administered as oral inhalations.” NCT05555290 ↗ “100 μg/ 90 μg salbutamol/albuterol Metered Dose Inhaler (MDI) or equivalent dose of Dry Powder Inhaler (DPI).” NCT00545272 ↗ “Subjects will also be given a short-acting beta agonist, albuterol (2 puffs, 180 mcg) prior to bronchoscopy.” NCT02401074 ↗ “Salbutamol/albuterol will be supplied to all subjects for use as rescue medication during the study.” NCT03287310 ↗ “The short-acting β2-agonist salbutamol/albuterol was available for rescue use throughout the study.” NCT00669617 ↗ “albuterol MDI 90 mcg OR or salbutamol HFA MDI 100 mcg for rescue medication, taken as directed” NCT01615874 ↗ “budesonide/albuterol sulfate pressurized inhalation suspension metered dose inhaler (BDA MDI)” NCT03934333 ↗ “the study intervention of 15 mg of albuterol diluted in 22 ml of magnesium sulfate solution” NCT01515995 ↗ “Salbutamol/albuterol was available for rescue medication use throughout the study.” NCT01120691 ↗ “Albuterol extended release belongs to a class of drugs known as bronchodilators.” NCT00755079 ↗ “salbutamol/albuterol given as a rescue medication via inhaler when needed” NCT01613326 ↗ “Albuterol/salbutamol will be supplied as inhalation aerosol or nebulizer.” NCT02889809 ↗ “PROAIR® HFA (Albuterol Sulfate) Inhalation Aerosol, eq 90 mcg Base” NCT03549897 ↗ “Budesonide/albuterol pressurized inhalation suspension, HFO” NCT06502366 ↗ “or be converted to budesonide/albuterol as rescue therapy” NCT07052942 ↗ “Albuterol Syrup (1mL= Salbutamol 0.4mg, 60ml/bot)” NCT02405598 ↗ “Albuterol DPI with 180 mcg Albuterol/inhalation” NCT01189396 ↗ “albuterol hydrofluoroalkane (HFA) inhalers” PMID 27523719 ↗ Aug 2016 “as-needed albuterol 180 µg” PMID 41791845 ↗ Mar 2026 “Salbutamol (Albuterol)” NCT00673621 ↗ “Salbutamol (Albuterol)” NCT07350421 ↗ “salbutamol/ albuterol” NCT02127697 ↗ “Salbutamol/Albuterol” NCT03363191 ↗ “Salbutamol/albuterol” NCT01854047 ↗ “Albuterol” NCT03549897 ↗ |
| Known as | Albuterol eMDPI | “Albuterol sulfate electronic multidose dry powder inhaler (Albuterol eMDPI) DS with 4 component devices:” NCT03890666 ↗ |
| Known as | Albuterol eMDPI DS | “Albuterol sulfate electronic multidose dry powder inhaler (Albuterol eMDPI) DS with 4 component devices:” NCT03890666 ↗ |
| Known as | Albuterol HCl | “Albuterol HCl Inhalation Solution” NCT00685126 ↗ |
| Known as | albuterol MDPI | “OBJECTIVE: To evaluate albuterol MDPI efficacy and safety in patients with exercise-induced bronchoconstriction (EIB).” PMID 26475054 ↗ Sep 2015 |
| Known as | Albuterol Spiromax | “Albuterol Spiromax is an inhalation-driven, multi-dose dry powder inhaler (DPI) containing a blend of albuterol sulfate with alpha-lactose monohydrate.” NCT01791972 ↗4“Albuterol Spiromax® 180 mcg (administered as 2 actuations of 90 mcg of albuterol base/actuation ex-mouthpiece) orally inhaled, single dose” NCT01844401 ↗ “Open-Label Assessment of the Albuterol Spiromax® Dry Powder Inhaler (DPI)” NCT01857323 ↗ “Albuterol Spiromax® delivers 90 mcg albuterol per inhalation.” NCT01058863 ↗ |
| Known as | albuterol Sulfate | “Study to demonstrate the comparability of two puffs of Combivent hydrofluoroalkane (HFA) inhalation aerosol (18 mcg ipratropium bromide/100 mcg albuterol sulfate / per puff) to...” NCT02182674 ↗42“The objective of this study was to investigate the bioequivalence of Mylan's albuterol sulfate extended-release 8 mg tablets to Pliva's VoSpire™ ER 8 mg tablets following a...” NCT00649779 ↗ “This is a Phase 3B, 12-week, multicenter, open-label study to evaluate the relationship between albuterol sulfate (ABS) eMDPI and clinical asthma exacerbation (CAE) in adult...” NCT02969408 ↗ “Albuterol sulfate inhalation aerosol 108 mcg/inhalation was administered via inhalation at a dose of 2 inhalations every 4 to 6 hours as rescue medication among participants...” NCT00550550 ↗ “Albuterol sulfate inhalation aerosol 108 mcg/inhalation was administed via inhalation at a dose of 2 inhalations every 4 to 6 hours, as needed, as rescue medication for asthma.” NCT00562159 ↗ “Measurements were made at baseline and at 30, 60 and 90 min following the administration of a nebulized β(2)-agonist (albuterol sulfate, 2.5 mg diluted in 3 ml normal saline).” PMID 21889619 ↗ Aug 2011 “Co-suspension Delivery™ Technology has been developed for the administration of albuterol sulfate pressurised inhalation suspension via metered-dose inhaler (AS MDI, PT007).” PMID 34089147 ↗ Jun 2021 “Co-suspension Delivery™ Technology has been developed for the administration of albuterol sulfate pressurised inhalation suspension via metered-dose inhaler (AS MDI, PT007).” PMID 34089147 ↗ Jun 2021 “The drug product albuterol sulfate DPI, TBS-7, is a single dose inhalation product of albuterol sulfate containing 240 ug albuterol sulphate (200 ug of albuterol)” NCT01252758 ↗ “Participants will receive Albuterol Sulfate MDI 90 μg per Actuation 1 to 6 doses (2 inhalations/dose) per day as needed via Oral inhalation route.” NCT05505734 ↗ “Combination Product: Budesonide/albuterol sulfate metered-dose inhaler 80/90 μg per puff. Two puffs to administer 160/180 μg dose.” NCT04848662 ↗ “Albuterol sulfate electronic multidose dry powder inhaler (Albuterol eMDPI) Digital System (DS) with 3 component devices:” NCT05241288 ↗ “Albuterol sulfate electronic multidose dry powder inhaler (Albuterol eMDPI) DS with 4 component devices:” NCT03890666 ↗ “fluticasone propionate (Fp) and albuterol sulfate (ABS), delivered in combination” NCT06290102 ↗ “Albuterol sulfate, USP, solution for inhalation will be diluted as follows:” NCT00434993 ↗ “3. albuterol sulfate as needed for relief of acute respiratory symptoms” NCT03952286 ↗ “Albuterol sulfate, a β2-adrenergic agonist, reduces IL-12 expression” PMID 20837847 ↗ Sep 2010 “PROAIR® HFA (Albuterol Sulfate) Inhalation Aerosol, eq 90 mcg Base” NCT03549897 ↗ “PROAIR™ HFA (Albuterol Sulfate) Breath Actuated Inhalation Aerosol” NCT00308685 ↗ “Albuterol Sulfate, 2.5 Mg/3 mL (0.083%) Inhalation Solution” NCT06271408 ↗ “Albuterol Sulfate, 2.5 Mg/3 mL (0.083%) Inhalation Solution” NCT06946264 ↗ “Albuterol Sulfate Inhalation Aerosol (90 mcg per actuation)” NCT06154304 ↗ “Ipratropium bromide 18 mcg and albuterol sulfate 103 mcg” NCT00462540 ↗ “Albuterol Sulfate metered dose inhaler [AS MDI] - PT007)” NCT06644924 ↗ “Treatment C (Albuterol Sulfate metered dose inhaler)” NCT03772223 ↗ “fluticasone propionate/albuterol sulfate combination” NCT06664619 ↗ “Albuterol Sulfate Extended-Release Tablets 8 mg” NCT00649987 ↗ “Albuterol sulfate metered-dose inhaler (AS MDI)” NCT06307665 ↗ “Albuterol sulfate inhalation aerosol” NCT03769090 ↗ “Albuterol Sulfate (Provenetil-HFA)” NCT00634829 ↗ “Salbutamol(Albuterol) Sulfate” NCT03098680 ↗ “Drug: albuterol Sulfate” NCT00667797 ↗ “Drug: Albuterol Sulfate” NCT00665600 ↗ |
| Known as | Albuterol Sulfate Acu-30 DPI | “A Stepwise, Rising Dose Study of Male Subjects With Mild Intermittent Asthma to Assess the Topical Safety and Tolerability of Albuterol Sulfate Acu-30™ DPI Compared With...” NCT00565591 ↗ |
| Known as | Albuterol Sulfate HFA | “Proair HFA (Albuterol Sulfate) or FDA authorized generic: Albuterol Sulfate HFA (Teva Pharmaceutical USA, Inc.) Inhalation Aerosol 108 mcg per actuation” NCT04912596 ↗ |
| Known as | albuterol sulphate | “The drug product albuterol sulfate DPI, TBS-7, is a single dose inhalation product of albuterol sulfate containing 240 ug albuterol sulphate (200 ug of albuterol)” NCT01252758 ↗1“Albuterol-sulphate (Proventil ®) Beta-2-adrenergic agonist 2.5 mg 3 cc inhalation Peak effect 15 - 30 mins. Mean duration of effect 3 hours” NCT01987219 ↗ |
| Known as | Albuterol-HFA | “This 12-week clinical study evaluates the safety and efficacy of Albuterol Sulfate HFA Inhalation Aerosol (Albuterol-HFA, or: A004), Armstrong's proposed HFA formulation of...” NCT00635505 ↗ |
| Known as | Albuterol/Salbutamol | ClinicalTrials.gov intervention name — accepted as the source's own label NCT02478398 ↗ |
| Known as | Armstrong Albuterol HFA | “albuterol (Armstrong Albuterol HFA)” NCT00634829 ↗ |
| Known as | AS MDI | “Co-suspension Delivery™ Technology has been developed for the administration of albuterol sulfate pressurised inhalation suspension via metered-dose inhaler (AS MDI, PT007).” PMID 34089147 ↗ Jun 20212“Albuterol Sulfate metered dose inhaler [AS MDI] - PT007)” NCT06644924 ↗ “Albuterol sulfate AS MDI (PT007)” NCT03847896 ↗ |
| Known as | etinoline | “At the acute stage of asthma : etinoline,twice a day for 7 days” NCT02341573 ↗ |
| Known as | Meptin swinghaler | ClinicalTrials.gov intervention name — accepted as the source's own label NCT01095016 ↗ |
| Known as | Pro-Air | “Albuterol (Pro-Air) hydrofluoroalkane (HFA) metered dose inhaler (MDI), was provided to be used as needed for the relief of asthma symptoms during both the run-in and treatment...” NCT01772368 ↗ |
| Known as | PROAIR HFA | “Proair HFA (Albuterol Sulfate) or FDA authorized generic: Albuterol Sulfate HFA (Teva Pharmaceutical USA, Inc.) Inhalation Aerosol 108 mcg per actuation” NCT04912596 ↗6“ProAir® HFA 180 mcg (administered as 2 actuations of 90 mcg of albuterol base/actuation ex-mouthpiece) orally inhaled, single dose” NCT01844401 ↗ “PROAIR® HFA (Albuterol Sulfate) Inhalation Aerosol, eq 90 mcg Base” NCT03549897 ↗ “PROAIR™ HFA (Albuterol Sulfate) Breath Actuated Inhalation Aerosol” NCT00308685 ↗ “ProAir® HFA delivers 90 mcg of albuterol per inhalation.” NCT01058863 ↗ “PROAIR® HFA (albuterol sulfate) Inhalation Aerosol” NCT03528577 ↗ |
| Known as | ProAir RespiClick | “ProAir® RespiClick, Albuterol multi-dose dry powder inhaler (MDPI)” NCT01857323 ↗ |
| Known as | ProAir RespiClick, Albuterol multi-dose dry powder inhaler (MDPI) | “ProAir® RespiClick, Albuterol multi-dose dry powder inhaler (MDPI)” NCT01218009 ↗1“ProAir® RespiClick, Albuterol multi-dose dry powder inhaler (MDPI)” NCT01058863 ↗ |
| Known as | Proventil | “The effects of albuterol delivered via AS MDI and Proventil on bronchodilation were equivalent, supporting the selection of AS MDI 180 µg to be taken into Phase III clinical...” PMID 34089147 ↗ Jun 2021 |
| Known as | Proventil HFA | “A recent study demonstrated that patients with mild asthma and the Arg/Arg variant at the 16th amino acid position have improved lung function and asthma control when albuterol...” NCT00521222 ↗2“A006 (Albuterol Dry Powder Inhaler (DPI)), in comparison with those of an active control, Proventil-HFA (Albuterol Metered Dose Inhaler (MDI))” NCT01189396 ↗ “Proventil® HFA (albuterol sulfate) Inhalation Aerosol (Key Pharmaceuticals) was used as rescue medication in this study.” NCT00577655 ↗ |
| Known as | PT007 | “Co-suspension Delivery™ Technology has been developed for the administration of albuterol sulfate pressurised inhalation suspension via metered-dose inhaler (AS MDI, PT007).” PMID 34089147 ↗ Jun 20212“Albuterol Sulfate metered dose inhaler [AS MDI] - PT007)” NCT06644924 ↗ “Albuterol sulfate AS MDI (PT007)” NCT03847896 ↗ |
| Known as | Racemic albuterol | “Racemic albuterol (0.63, 1.25 mg or 2.5 mg); the first three doses will be delivered every 20 minutes for the first hour.” NCT00685126 ↗ |
| Known as | racemic salbutamol | ClinicalTrials.gov intervention name — accepted as the source's own label NCT00830882 ↗ |
| Known as | S-albuterol | ClinicalTrials.gov intervention name — accepted as the source's own label NCT00320034 ↗ |
| Known as | SALB | “Or nebulized combination ipratropium bromide with salbutamol (IB+SALB; 0.5mg/2mL + 2.5mg/2.5mL).” NCT02782052 ↗ |
| Known as | SalbG | “(Salbutamol Generic, SalbG)” NCT05884970 ↗ |
| Known as | SalbR | “reference product (Ventolin, Salbutamol Reference, SalbR)” NCT05884970 ↗ |
| Known as | Salbultamol | ClinicalTrials.gov intervention name — accepted as the source's own label NCT00990847 ↗ |
| Known as | Salbutamol Generic | “(Salbutamol Generic, SalbG)” NCT05884970 ↗ |
| Known as | Salbutamol Reference | “reference product (Ventolin, Salbutamol Reference, SalbR)” NCT05884970 ↗ |
| Known as | Salbutamol Sandoz | “"100 mcg Salbutamol Sandoz" and "300 mcg Salbutamol Sandoz"” NCT05884970 ↗ |
| Known as | Salbutamol Sulfate | “Each participant received aerosolized salbutamol sulfate consisting of 1 mL Farcolin® solution containing 6050 µg salbutamol sulfate diluted with 2 mL normal saline placed...” NCT07633223 ↗8“Nebulized bronchodilator drugs will be Salbutamol Sulfate (aerolin nebulis) and ipratropium bromide (atrovent) diluted in a saline solution (saline 0.9%) in 3 ml.” NCT03271905 ↗ “Nebulization of ipratropium bromide/salbutamol sulfate (500 µg/2.5 mg) before the administration of the Glittre ADL-test” NCT03071731 ↗ “Salbutamol will be delivered using a Babyhaler spacer device. Ventolin will be used, brandname for Salbutamol sulfate.” NCT04584034 ↗ “Fluticasone Propionate/Salbutamol Sulfate. Oral inhalation powder.” NCT06052267 ↗ “Salbutamol sulfate 120 mcg + Ipratropium bromide 20 mcg per puff” NCT02182713 ↗ “Salbutamol (as Salbutamol Sulfate) 2 Mg Oral Tablet” NCT05099107 ↗ “Ventolin® MDI * Ingredient: Salbutamol sulfate” NCT01076322 ↗ |
| Known as | salbutamol sulphate | “As needed use of salbutamol sulphate aerosol (Ventolin) when exacerbation happens” NCT03842839 ↗5“120 mcg salbutamol sulphate (equivalent to 100 mcg of the base)” NCT02182713 ↗ “Salbutamol sulphate (2.5 mg) + ipratropium bromide (0.5 mg)” NCT06825013 ↗ “VENTOLIN TABLETS 2MG (SALBUTAMOL SULPHATE)” NCT02405598 ↗ “Drug: Salbutamol sulphate” NCT01521572 ↗ |
| Known as | Salbutamol Sulphate BP | “Salbutamol 5mg/2.5ml Nebulizer Solution (one Ventolin nebule containing a preservative-free solution of Salbutamol Sulphate BP 2.5mg, GlaxoSmithKline Inc.)” NCT03333395 ↗ |
| Known as | Salbutamol Sulphate Inhalation Aerosol (Ventolin) | “Salbutamol Sulphate Inhalation Aerosol (Ventolin®)” NCT03169504 ↗ |
| Known as | Salbutamol Ventolin GSK | “"100 mcg Salbutamol Ventolin GSK" and "300 mcg Salbutamol Ventolin GSK"” NCT05884970 ↗ |
| Known as | TBS-7 | “The drug product albuterol sulfate DPI, TBS-7, is a single dose inhalation product of albuterol sulfate containing 240 ug albuterol sulphate (200 ug of albuterol)” NCT01252758 ↗ |
| Known as | Ventilastin | “Salbutamol inhaler (200 µg per puff; a short acting β2-agonist; Ventilastin®).” NCT00633919 ↗ |
| Known as | Ventolin | “cough medicine (such as codeine), bronchodilators (such as ventolin), expectorants (such as fluimucil) and so on are used to treat cough, shortness of breath, or other...” NCT06095258 ↗22“Patients assigned to the active group will be treated with 0.15 mg/kg body weight (diluted in 3 mL 0.9% NaCl) nebulized salbutamol (Ventolin®, GlaxoSmithKline, Dublin, Ireland)...” NCT05527704 ↗ “Salbutamol 5mg/2.5ml Nebulizer Solution (one Ventolin nebule containing a preservative-free solution of Salbutamol Sulphate BP 2.5mg, GlaxoSmithKline Inc.)” NCT03333395 ↗ “The bronchodilator used in the study is the Salbutamol as Ventolin ® (GSK) suspension for inhalation as an aerosol at a dose of 100μg per puff.” NCT01470755 ↗ “Salbutamol will be delivered using a Babyhaler spacer device. Ventolin will be used, brandname for Salbutamol sulfate.” NCT04584034 ↗ “Nebulized salbutamol (Ventolin respiratory solution) 2.5 mg stat and once only with standard care” NCT02160548 ↗ “Salbutamol will be used to Group A patients: Salbutamol (Ventolin®, GlaxoSmithKline) 100μg/dose.” NCT03745261 ↗ “Ipratropium Bromide (Atrovent) & Albuterol (Ventolin) as Standard of Care” NCT04655170 ↗ “The drugs used by the children were zespira and ventolin.” NCT05930847 ↗ “Ventolin tb, syrup, intravenous(IV),5mgx10 ampule(amp)” NCT00628758 ↗ “Tiotropium (Spiriva) + Salbutamol (Ventolin)” NCT00981851 ↗ “VENTOLIN TABLETS 2MG (SALBUTAMOL SULPHATE)” NCT02405598 ↗ “100 μg of albuterol (Ventolin®)” NCT01112241 ↗ “Salbutamol (Ventolin®)” NCT07591558 ↗ “Salbutamol (Ventolin®)” NCT06918418 ↗ “Salbutamol (Ventolin®)” NCT07378605 ↗ “Salbutamol (Ventolin®)” NCT06921291 ↗ “Ventolin” NCT01997463 ↗ |
| Known as | Ventolin (salbutamol) | “Ventolin (salbutamol)” NCT00876135 ↗1“VENTOLIN (salbutamol)” NCT03924635 ↗ |
| Known as | ventolin 2.5 Nebules 2.5mg/2.5 ml | “2.5 mL solution containing salbutamol (ventolin 2.5 Nebules 2.5mg/2.5 ml, a bronchodilator)” NCT02159196 ↗ |
| Known as | Ventolin MDI | “Ventolin® MDI * Ingredient: Salbutamol sulfate” NCT01076322 ↗ |
| Known as | Ventoline | “The purpose of the project is to investigate whether the use of a WADA approved dose of salbutamol (albuterol/Ventoline) has a performance-enhancing effect on sprint...” NCT04402658 ↗ |
| Known as | VentolinTM | “Salbutamol (VentolinTM) is a short acting beta agonist (SABA) which is used to treat wheezing, dyspnea and breathing difficulties caused by asthma and COPD.” NCT00911651 ↗ |
| Known as | Volmax | “Volmax tb 4 mg/8 mg” NCT00628758 ↗ |
| Known as | VoSpire ER | “The objective of this study was to investigate the bioequivalence of Mylan's albuterol sulfate extended-release 8 mg tablets to Pliva's VoSpire™ ER 8 mg tablets following a...” NCT00649779 ↗ |
| Action | Inhibit | “reduces IL-12 expression” PMID 20837847 ↗ Sep 2010 |
| Modality | Other / unclassified | “aerosolized β₂-agonist” PMID 21562125 ↗ Sep 2011 |
| Route | Inhaled | “inhaled albuterol” NCT00000577 ↗ |