Salbutamol
Regulatory milestones approvals, filings & regulatory actions · 15 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Label expansion | US (FDA) | PROAIR RESPICLICK | — | 2016-04-28 | fda.gov ↗ |
| Filed | US (FDA) | ProAir® RespiClick | asthma, exercise-induced bronchoconstriction | 2015-09-10 | “the U.S. Food and Drug Administration (FDA) has accepted for review the company’s supplemental new drug application (sNDA) for ProAir® RespiClick (albuterol sulfate) Inhalation Powder” tevapharm.com ↗ |
| Filed | US (FDA) | — | asthma, exercise-induced bronchoconstriction | 2014-07-14 | “the U.S. Food and Drug Administration (FDA) has accepted for review the company’s new drug application (NDA) for albuterol multi-dose dry-powder inhaler (MDPI)” tevapharm.com ↗ |
| 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 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 198 · 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| Phase 0 | NCT03889379 | Jan 2019 → Jun 2021 | — | University of Arizona | Withdrawn | No outcome recorded |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 | Mixed |
| 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 Stop: Enrollment |
| 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 | NCT00649779 | Sep → Oct 2005 | — | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1 | NCT00649987 | 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 · 4 met primary · 1 missed | ||||||
| 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 | Met primary |
| Phase 2 | NCT03364608 | Dec 2017 → Mar 2018 | asthma | AstraZeneca | Completed | Met primary |
| 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 | NCT01174732 | Jul → Oct 2010 | asthma | Amphastar Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01189396 | Jul → Dec 2010 | asthma, chronic obstructive pulmonary disease | Amphastar Pharmaceuticals, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01058863 | Feb → Jun 2010 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | Met primary |
| Phase 2 | NCT00818454 | Dec 2008 → Sep 2009 | asthma | Boehringer Ingelheim | Completed | Met primary |
| 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 | Missed primary |
| Phase 2 | NCT00320034 | Apr 2006 → Jun 2008 | asthma | Hamilton Health Sciences Corporation | Completed | No outcome recorded |
| Phase 2 | NCT00358488 | Apr 2006 → Jan 2007 | chronic obstructive pulmonary disease | GlaxoSmithKline | 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 Stop: Enrollment |
| Phase 2/3 | NCT00755079 | Apr 2007 → Aug 2012 | spinal cord injury | US Department of Veterans Affairs | Completed | No outcome recorded |
| Phase 347 trials · 13 met primary | ||||||
| Phase 3 | NCT06664619 | Dec 2024 → Nov 2026 expected | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Active not recruiting | No outcome recorded |
| Phase 3 | NCT06261957 | May 2024 → Sep 2025 | asthma | GlaxoSmithKline | Completed | Met primary |
| 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 | Met primary |
| 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 Stop: Enrollment |
| Phase 3 | NCT05505734 | Sep 2022 → Aug 2024 | asthma | Bond Avillion 2 Development LP | Completed | Met primary |
| 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 | Met primary |
| 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 | Mixed |
| 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 | Met primary |
| 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 | Met primary |
| Phase 3 | NCT01857323 | May → Aug 2013 | asthma, chronic obstructive pulmonary disease | 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 | NCT01791972 | Mar → May 2013 | exercise-induced bronchoconstriction | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | Met primary |
| Phase 3 | NCT01747629 | Dec 2012 → Oct 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | Met primary |
| Phase 3 | NCT01424813 | Dec 2012 → Oct 2013 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | Met primary |
| 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 | 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 | Met primary |
| Phase 3 | NCT00400153 | Nov 2006 → Apr 2008 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | Met primary |
| Phase 3 | NCT00308685 | Jun → Dec 2006 | asthma | Teva Branded Pharmaceutical Products R&D, Inc. | Completed | Met primary |
| 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 | Met primary |
| 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 · 2 met primary · 2 missed | ||||||
| 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 Stop: Enrollment |
| 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 | Missed primary |
| 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 | Missed primary |
| 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 | Met primary |
| 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 | Met primary |
| 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 · 2 met primary · 1 missed | ||||||
| — | 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 | Met primary |
| — | 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 | Missed primary |
| — | 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 | Met primary |
| — | 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 |
| Comparator or background therapy221 trials | ||||||
| Phase 0 | NCT04901715 Comparator | Jun 2021 → Jul 2024 | primary ciliary dyskinesia | University of North Carolina, Chapel Hill | Completed | No outcome recorded |
| 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 Stop: Business |
| 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 |
| Show all 221 trials opens the full record — a long page | ||||||
News releases announcing trial results or a regulatory action · 27
| Date | Issuer | Release |
|---|---|---|
| 2025-10-22 | GlaxoSmithKline | Results GSK announces positive pivotal phase III data for next-generation low carbon version of Ventolin (salbutamol) metered dose inhaler gsk.com ↗
Data confirm that the formulation of salbutamol MDI containing an innovative low carbon propellant HFA-152a shows therapeutic equivalence and is comparable in safety to salbutamol MDI containing the current propellant, HFA-134a. |
| 2025-05-19 | AstraZeneca | Results Statistically significant and clinically meaningful BATURA Phase III trial results provide new evidence for Airsupra as standard of care for as-needed rescue treatment in asthma astrazeneca.com ↗
The BATURA trial demonstrated treatment with Airsupra significantly reduced the risk of a severe exacerbation by 47% (5.1%, 9.1%, hazard ratio [HR] 0.53; 95% confidence interval [CI], 0.39, 0.73; p<0.001) when compared with albuterol alone. |
| 2024-10-07 | AstraZeneca | Results Airsupra demonstrated statistically significant and clinically meaningful reduction in the risk of severe exacerbations in patients with intermittent or mild persistent asthma in BATURA Phase III trial astrazeneca.com ↗
Independent Data Monitoring Committee recommended trial stop early due to overwhelming efficacy at pre-planned analysis |
| 2024-10-06 | DevPro Biopharma | Results DevPro Biopharma and Bespak Complete Early Feasibility Studies devprobiopharma.com ↗
DevPro Biopharma and Bespak Complete Early Feasibility Studies |
| 2024-05-22 | Amphastar Pharmaceuticals, Inc. | Regulatory Amphastar Receives FDA Approval for Albuterol Sulfate Inhalation Aerosol amphastar.com ↗
Amphastar Pharmaceuticals, Inc. (NASDAQ:AMPH) today announced that the U.S. Food and Drug Administration ("FDA") has granted approval for the Company's Abbreviated New Drug Application ("ANDA") for Albuterol Sulfate Inhalation Aerosol, previously known as AMP-008. |
| 2023-01-11 | AstraZeneca | Regulatory Airsupra (PT027) approved in the US for asthma astrazeneca.com ↗
Airsupra (albuterol/budesonide), formerly known as PT027, has been approved in the US for the as-needed treatment or prevention of bronchoconstriction and to reduce the risk of exacerbations in people with asthma aged 18 years and older. |
| 2022-11-09 | AstraZeneca | Regulatory PT027 recommended by FDA Advisory Committee as new rescue treatment for asthma astrazeneca.com ↗ |
| 2022-09-07 | Teva Branded Pharmaceutical Products R&D, Inc. | Results 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 ↗
The study found patients who used the ProAir Digihaler had reductions in weekly average daily short-acting beta agonist (SABA) inhalations and an increase in weekly number of SABA-free days. |
| 2022-05-17 | Teva Branded Pharmaceutical Products R&D, Inc. | Results Teva Announces New Findings Highlighting Potential of ProAir® Digihaler® (albuterol sulfate) Inhalation Powder to Address Asthma Treatment Challenges tevapharm.com ↗
Among the study findings, nearly one-third of asthma patients made 138 or more inhalations during the 12-week study period, which was equivalent to 600 or more inhalations, or three or more canisters, per year. |
| 2022-05-15 | AstraZeneca | Results PT027, a novel fixed-dose combination of albuterol and budesonide, used as an as-needed rescue medicine, significantly reduced the risk of a severe exacerbation compared to albuterol by 27% in patients with asthma astrazeneca.com ↗
Compared with albuterol rescue, PT027 at the 180mcg albuterol/160mcg budesonide dose reduced the risk of a severe exacerbation by 27% (p<0.001) in adults and adolescents. |
| 2021-09-09 | AstraZeneca | Results Fixed-dose combination of albuterol and budesonide (PT027) demonstrated significant benefits for asthma patients in MANDALA and DENALI Phase III trials astrazeneca.com ↗
The MANDALA trial met the primary endpoint, with PT027 demonstrating statistically significant and clinically meaningful reductions in the risk of severe exacerbations compared to albuterol, when used as a rescue medicine in response to symptoms. |
| 2021-05-10 | Teva Branded Pharmaceutical Products R&D, Inc. | Results Teva to Highlight Research in Respiratory Care at Upcoming 2021 American Thoracic Society International Conference tevapharm.com ↗
Teva Pharmaceuticals, a U.S. affiliate of Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA),today announced that it will present two new e-posters at the upcoming American Thoracic Society (ATS) International Conference, taking place virtually May 14-19, 2021. |
| 2021-03-15 | CuraSen Therapeutics, Inc. | Results CuraSen Therapeutics Announces Phase 1 Clinical Data Demonstrating that Salbutamol, a Beta-2 Adrenoceptor Agonist, Significantly Increases Cerebral Perfusion, a Key Marker in Neurodegenerative Disease curasen.com ↗
CuraSen Therapeutics, Inc., a privately held, clinical-stage biotechnology company, announced Phase 1 proof-of-principle data demonstrating that salbutamol, a drug approved to treat respiratory disease, significantly improved brain perfusion as measured by increased cerebral blood flow (CBF) in healthy subjects. |
| 2020-08-25 | Lupin Limited | Regulatory Lupin Receives Approval for Generic Albuterol Sulphate MDI lupin.com ↗
Lupin Limited (Lupin) announced today that it has received approval from the United States Food and Drug Administration (U.S. FDA) for its Albuterol Sulfate Inhalation Aerosol, 90 mcg (base)/actuation, a generic version of ProAir® HFA. |
| 2020-05-19 | Teva Canada | Regulatory Teva Canada Secures Salbutamol Inhalers from its Global Supply Chain to Mitigate Shortage in Canadian Market tevacanada.com ↗
Working closely with Health Canada and through the Interim Order, Teva Canada was able to expedite approval to import a supply of Pr Salamol CFC-Free Inhaler to Canada. |
| 2019-05-20 | AstraZeneca | Results New data show Symbicort reduces attacks in mild asthma when used as an anti-inflammatory reliever astrazeneca.com ↗
Symbicort Turbuhaler demonstrated a 51% reduction in the rate of annual asthma exacerbations compared to albuterol. |
| 2018-12-21 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory 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. | Regulatory 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. | Regulatory Teva Announces FDA Acceptance of a Supplemental New Drug Application for ProAir® RespiClick (albuterol sulfate) Inhalation Powder for Pediatric Patients tevapharm.com ↗
“The acceptance of the pediatric filing for ProAir® RespiClick by the FDA represents an important step forward for Teva in our mission to better serve patients living with respiratory conditions, such as asthma and EIB,” |
| 2015-04-01 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Announces FDA Approval of ProAir® RespiClick tevapharm.com ↗ |
| 2014-07-31 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Reports Second Quarter 2014 Results tevapharm.com ↗
the FDA acceptance of our albuterol MDPI NDA |
| 2014-07-14 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Announces FDA Acceptance of NDA Filing for Investigational Short-Acting Beta-Agonist (SABA) Inhaler (Albuterol MDPI) tevapharm.com ↗
The NDA for albuterol MDPI has been accepted by the FDA for standard review, with a FDA Regulatory Action expected in March 2015. |
| 2013-11-08 | Teva Branded Pharmaceutical Products R&D, Inc. | Results Survey Data Reinforces Patient Benefit of Asthma Rescue Inhalers with Integrated Dose Counters tevapharm.com ↗
The incidence rate of respiratory-related ER visits in the total study population was estimated to be 45 percent lower in the dose counter cohort compared with the non-dose counter cohort. |
| 2011-10-07 | Boehringer Ingelheim | Regulatory FDA Approves Combivent® Respimat® (ipratropium bromide and albuterol) Inhalation Spray for the Treatment of Patients with Chronic Obstructive Pulmonary Disease prnewswire.com ↗ |
| 2010-04-13 | Boehringer Ingelheim | Regulatory FDA Maintains Essential Use Status of Combivent(R) (ipratropium bromide and albuterol sulfate) Inhalation Aerosol Through 2013 prnewswire.com ↗ |
| 2008-09-24 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva's Proair® HFA, the Market Leading Albuterol Inhaler, Receives New Pediatric Indication tevapharm.com ↗
Teva Pharmaceutical Industries Ltd. today announced that the U.S. Food and Drug Administration (FDA) has approved ProAir® HFA (albuterol sulfate) Inhalation Aerosol for use in patients as young as 4 years of age. |
| 2008-01-02 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Announces Approval Of Generic Duoneb® tevapharm.com ↗
Teva Pharmaceutical Industries Ltd. (Nasdaq: TEVA)announced today that the U.S. Food and Drug Administration (FDA) has granted final approval for the Company's Abbreviated New Drug Application(ANDA) to market its generic version of Dey's bronchodilator, DuoNeb® (Albuterol Sulfate and Ipratropium Bromide) Inhalation Solution, 3 mg (0.083%)and 0.5 mg (0.017%). |
All press releases naming this drug 37 releases
Evidence & citations 56 cited values
Every value below carries the sentence it was read from. 430 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...” NCT02139644 ↗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...” NCT01479621 ↗ “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 ↗ “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 ↗ “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 ↗ “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 ↗ |
| 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 | 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 2007212“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 ↗ |
| 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 ↗3“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 ↗43“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 ↗ |
| 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-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-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/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 | 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 ↗5“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 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 | 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 ↗23“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 ↗ “Albuterol sulfate inhalation aerosol (Ventolin®), 100 μg per actuation.” NCT07807007 ↗ “The drugs used by the children were zespira and ventolin.” NCT05930847 ↗ “Ventolin tb, syrup, intravenous(IV),5mgx10 ampule(amp)” NCT00628758 ↗ |
| Known as | VENTOLIN (salbutamol) | “VENTOLIN (salbutamol)” NCT03924635 ↗1“Ventolin (salbutamol)” NCT00876135 ↗ |
| 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 ↗ |