Formoterol
Regulatory milestones approvals, filings & regulatory actions · 5 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Filed asthma 2 milestones | |||||
| Filed | UK (MHRA) | Bufomix Easyhaler | asthma | 2016-02-02 | “we have submitted a marketing authorisation application for the budesonide-formoterol combined formulation in Germany, the United Kingdom and France.” orionpharma.com ↗ |
| Filed | EU (EMA) | — | asthma | 2013-03-21 | “Orion Corporation has submitted a marketing authorisation application for combined budesonide-formoterol formulation of the Easyhaler® product family in Europe.” orionpharma.com ↗ “LAS40464, the combination of aclidinium with formoterol which has been filed for registration in the EU” astrazeneca.com ↗ |
| Approved Indication not stated 3 milestones | |||||
| Approved | EU (EMA) | DuoResp Spiromax | — | 2014-04-28 | europa.eu ↗ |
| Label expansion | US (FDA) | FORADIL | — | 2003-06-27 | fda.gov ↗ |
| Approved | US (FDA) | FORADIL | — | 2001-02-16 | fda.gov ↗ |
Trials 265 · started per year
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 126 trials · 1 missed | ||||||
| Phase 1 | NCT07433569 | Mar → Jun 2026 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT06723756 | Jan → Jun 2025 | — | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT05898984 | Apr → Jul 2023 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 1 | NCT05830071 | Mar → Oct 2023 | asthma, chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 1 | NCT04600505 | Oct 2020 → May 2021 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT03906045 | Apr 2019 → Mar 2020 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT03859414 | Mar → Jul 2019 | asthma, chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 1 | NCT03795350 | Jan 2019 → Apr 2020 | asthma, chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Terminated | No outcome recorded |
| Phase 1 | NCT03740373 | Sep → Oct 2018 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT03311373 | Oct → Dec 2017 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT03250182 | Aug → Dec 2017 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT02975843 | Nov 2016 → Mar 2017 | asthma, chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 1 | NCT02631941 | Jan → Jul 2016 | asthma | Zambon SpA | Completed | Mixed |
| Phase 1 | NCT03073057 | Jan → Mar 2016 | asthma | Orion Corporation, Orion Pharma | Completed | No outcome recorded |
| Phase 1 | NCT02237508 | Sep 2014 → Feb 2015 | asthma | Zambon SpA | Completed | Missed primary |
| Phase 1 | NCT02197975 | Aug → Oct 2014 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT02196714 | Jul → Sep 2014 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 1 | NCT02119234 | Mar 2014 → Feb 2015 | chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 1 | NCT01423305 | Aug → Oct 2011 | asthma | Orion Corporation, Orion Pharma | Completed | No outcome recorded |
| Phase 1 | NCT01386996 | Jul → Nov 2011 | asthma | Orion Corporation, Orion Pharma | Completed | No outcome recorded |
| Phase 1 | NCT01181063 | Aug → Oct 2010 | asthma | Orion Corporation, Orion Pharma | Completed | No outcome recorded |
| Phase 1 | NCT00657774 | Apr → Sep 2008 | asthma | SkyePharma AG | Completed | No outcome recorded |
| Phase 1 | NCT00569712 | Jan 2007 → Dec 2008 | lung cancer, precancerous condition | British Columbia Cancer Agency | Completed | No outcome recorded |
| Phase 1 | NCT00418509 | Nov 2006 → ? | — | Novartis | Completed | No outcome recorded |
| Phase 1 | NCT00940329 | Apr → Jul 2004 | — | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT00280358 | ? → Dec 2005 | — | Dey | Completed | No outcome recorded |
| Phase 1/22 trials | ||||||
| Phase 1/2 | NCT06110403 | Sep 2023 → Sep 2026 overdue | chronic obstructive pulmonary disease | University Hospital, Lille | Recruiting | No outcome recorded |
| Phase 1/2 | NCT01176747 | Aug → Sep 2010 | asthma, chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 247 trials · 13 met primary | ||||||
| Phase 2 | NCT07301736 | Dec 2025 → Jun 2027 expected | asthma | Chiesi Farmaceutici S.p.A. | Recruiting | No outcome recorded |
| Phase 2 | NCT07022418 | Dec 2025 → Dec 2026 expected | diabetic kidney disease | Medical University of South Carolina | Recruiting | No outcome recorded |
| Phase 2 | NCT04087590 | Jan 2020 → Mar 2023 | chronic obstructive pulmonary disease | University Hospital, Lille | Terminated | No outcome recorded |
| Phase 2 | NCT03590379 | Jun → Oct 2018 | chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | Met primary |
| Phase 2 | NCT03276078 | Nov 2017 → Jun 2018 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT03086460 | Sep 2017 → Jul 2018 | asthma | Chiesi Farmaceutici S.p.A. | Completed | Met primary |
| Phase 2 | NCT03108534 | Feb → Sep 2017 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 2 | NCT02787967 | Aug 2016 → Jun 2017 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 2 | NCT02796651 | Jun → Dec 2016 | chronic obstructive pulmonary disease | AstraZeneca | Completed | Met primary |
| Phase 2 | NCT02196077 | Aug 2014 → Mar 2015 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT02148120 | Apr → Oct 2014 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 2 | NCT02048644 | Mar 2014 → Apr 2015 | idiopathic pulmonary fibrosis | Hull University Teaching Hospitals NHS Trust | Completed | No outcome recorded |
| Phase 2 | NCT01783821 | Jul 2013 → Jul 2015 | adult acute respiratory distress syndrome | Mayo Clinic | Completed | Met primary |
| Phase 2 | NCT01615874 | Jan → Sep 2013 | asthma | Organon and Co | Withdrawn | No outcome recorded |
| Phase 2 | NCT01738087 | Nov 2012 → Jan 2013 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 2 | NCT01641081 | Jun 2012 → Feb 2013 | asthma | AstraZeneca | Completed | Met primary |
| Phase 2 | NCT01650441 | Apr 2012 → Jun 2013 | asthma | University Hospital, Antwerp | Completed | No outcome recorded |
| Phase 2 | NCT01468272 | Nov 2011 → Aug 2012 | childhood onset asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 2 | NCT01349816 | Jun → Nov 2011 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | Met primary |
| Phase 2 | NCT01349803 | May → Nov 2011 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Completed | No outcome recorded |
| Phase 2 | NCT01349257 | May → Jun 2011 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 2 | NCT01256086 | Dec 2010 → Jul 2011 | asthma | MEDA Pharma GmbH & Co. KG | Completed | No outcome recorded |
| Phase 2 | NCT01258803 | Dec 2010 → Oct 2011 | asthma | Organon and Co | Completed | Met primary |
| Phase 2 | NCT01191424 | Oct 2010 → Sep 2011 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 2 | NCT01136655 | Sep 2010 → Dec 2011 | asthma | AstraZeneca | Completed | Met primary |
| Phase 2 | NCT01168310 | Aug 2010 | chronic obstructive pulmonary disease | Dey | Completed | No outcome recorded |
| Phase 2 | NCT01043601 | Jul 2010 → Apr 2011 | chronic obstructive pulmonary disease | Pearl Therapeutics, Inc. | Withdrawn | No outcome recorded |
| Phase 2 | NCT01113593 | May 2010 | chronic obstructive pulmonary disease | Dey | Completed | No outcome recorded |
| Phase 2 | NCT01048333 | Jan → May 2010 | chronic obstructive pulmonary disease | AstraZeneca | Completed | Met primary |
| Phase 2 | NCT00801684 | Feb → Apr 2009 | chronic obstructive pulmonary disease | Alkermes, Inc. | Completed | Met primary |
| Phase 2 | NCT00746330 | Aug 2008 → Apr 2009 | asthma | Novartis | Completed | No outcome recorded |
| Phase 2 | NCT00624754 | Mar 2008 → Jul 2012 | obstructive lung disease | Assistance Publique - Hôpitaux de Paris | Completed | Met primary |
| Phase 2 | NCT01343745 | Feb → Aug 2008 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 2 | NCT00635882 | Feb 2008 → Jun 2009 | asthma | Organon and Co | Completed | Met primary |
| Phase 2 | NCT00626522 | Feb → Nov 2008 | chronic obstructive pulmonary disease | AstraZeneca | Completed | Met primary |
| Phase 2 | NCT00443482 | Feb → May 2007 | asthma | Novartis | Completed | No outcome recorded |
| Phase 2 | NCT00403286 | Nov 2006 → May 2007 | chronic obstructive pulmonary disease | Dey | Completed | No outcome recorded |
| Phase 2 | NCT00314509 | Jul 2005 → Jan 2006 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT00215371 | Jul → Oct 2002 | asthma | Dey | Completed | No outcome recorded |
| Phase 2 | NCT00215358 | Jul → Oct 2002 | asthma | Dey | Completed | No outcome recorded |
| Phase 2 | NCT02238119 | Feb → Aug 2002 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2 | NCT02242240 | Mar → Dec 2001 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | No outcome recorded |
| Phase 2 | NCT00239278 | Jan 2001 → Jan 2005 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 2 | NCT00215397 | ? → Feb 2003 | asthma | Dey | Completed | No outcome recorded |
| Phase 2 | NCT00215384 | ? → Apr 2003 | chronic obstructive pulmonary disease | Dey | Completed | No outcome recorded |
| Phase 2 | NCT00215423 | ? → Dec 2003 | chronic obstructive pulmonary disease | Dey | Completed | No outcome recorded |
| Phase 2 | NCT00215410 | ? → Oct 2003 | asthma | Dey | Completed | No outcome recorded |
| Phase 2/34 trials · 1 met primary | ||||||
| Phase 2/3 | NCT04331470 | Apr 2020 | COVID-19 | Fasa University of Medical Sciences | Unknown | No outcome recorded |
| Phase 2/3 | NCT02693769 | Jul → Oct 2016 | asthma | Mundipharma Research Limited | Terminated | No outcome recorded Stop: Enrollment |
| Phase 2/3 | NCT02195375 | Sep 2014 → May 2016 | chronic obstructive pulmonary disease | Mundipharma Research Limited | Completed | No outcome recorded |
| Phase 2/3 | NCT00463567 | Apr 2007 → Aug 2008 | chronic obstructive pulmonary disease | Novartis | Completed | Met primary |
| Phase 3117 trials · 38 met primary · 5 missed | ||||||
| Phase 3 | NCT07858123 | Nov 2026 → Jun 2030 expected | asthma | Chiesi Farmaceutici S.p.A. | Not yet recruiting | No outcome recorded |
| Phase 3 | NCT05735431 | Jun 2026 → Nov 2027 | chronic asthma | Eurofarma Laboratorios S.A. | Withdrawn | No outcome recorded Stop: Business |
| Phase 3 | NCT06429475 | Jun 2024 → Dec 2028 expected | asthma | University of KwaZulu | Recruiting | No outcome recorded |
| Phase 3 | NCT06075095 | Jan 2024 → Aug 2025 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT04233190 | Apr 2023 → Oct 2024 | asthma | Eurofarma Laboratorios S.A. | Completed | No outcome recorded |
| Phase 3 | NCT05755906 | Feb 2023 → Nov 2024 | asthma | AstraZeneca | Completed | Met primary |
| Phase 3 | NCT05573464 | Sep 2022 → Mar 2024 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 3 | NCT05322707 | Apr 2022 → Aug 2023 | asthma | Cipla Ltd. | Completed | No outcome recorded |
| Phase 3 | NCT05202262 | Jan 2022 → Feb 2025 | asthma | AstraZeneca | Completed | Met primary |
| Phase 3 | NCT04705727 | Aug → Sep 2021 | childhood onset asthma | Centre Hospitalier Intercommunal Creteil | Terminated | No outcome recorded Stop: Enrollment |
| Show all 117 trials opens the full record — a long page | ||||||
| Phase 454 trials · 6 met primary · 2 missed | ||||||
| Phase 4 | NCT06531798 | Jan → Oct 2026 expected | chronic obstructive pulmonary disease | AstraZeneca | Recruiting | No outcome recorded |
| Phase 4 | NCT07073950 | Nov 2025 → May 2027 expected | chronic obstructive pulmonary disease | AstraZeneca | Recruiting | No outcome recorded |
| Phase 4 | NCT06590740 | Oct 2024 → Sep 2025 | cough variant asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT05970263 | Jan 2024 → Dec 2025 | chronic obstructive pulmonary disease | AstraZeneca | Withdrawn | No outcome recorded Stop: Enrollment |
| Phase 4 | NCT06571942 | Nov 2023 → Jan 2025 overdue | chronic obstructive pulmonary disease | National Institute of Respiratory Diseases, Mexico | Recruiting | No outcome recorded |
| Phase 4 | NCT05084222 | Nov 2021 → Jun 2023 | asthma | Orion Corporation, Orion Pharma | Completed | No outcome recorded |
| Phase 4 | NCT04671355 | Oct → Dec 2021 | chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Withdrawn | No outcome recorded |
| Phase 4 | NCT07809555 | Aug 2021 → Nov 2024 | lung disorder | Yi-Han Hsiao | Completed | No outcome recorded |
| Phase 4 | NCT04655170 | Dec 2020 → Jan 2023 overdue | chronic obstructive pulmonary disease | University of Tennessee Graduate School of Medicine | Recruiting | No outcome recorded |
| Phase 4 | NCT04159519 | Jul 2020 → Jan 2023 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT04271839 | Jun 2020 → May 2021 | chronic asthma | Mundipharma Pharmaceuticals S.L. | Withdrawn | No outcome recorded |
| Phase 4 | NCT04171180 | May → Sep 2020 | cough variant asthma | Second Affiliated Hospital, School of Medicine, Zhejiang University | Unknown | No outcome recorded |
| Phase 4 | NCT03662711 | Nov 2018 → Oct 2022 | chronic obstructive pulmonary disease | Università degli Studi di Ferrara | Terminated | No outcome recorded |
| Phase 4 | NCT03478696 | Jun 2018 → Mar 2019 | chronic obstructive pulmonary disease | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT03563001 | Jun → Sep 2018 | chronic obstructive pulmonary disease | Zhujiang Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT03551197 | Jun → Sep 2018 | chronic obstructive pulmonary disease | Zhujiang Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT03028701 | Sep 2015 → Mar 2017 | chronic obstructive pulmonary disease | Neutec Ar-Ge San ve Tic A.Ş | Completed | No outcome recorded |
| Phase 4 | NCT02934945 | Sep 2015 → Jan 2017 | asthma | Zhujiang Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT02424344 | Apr 2015 → Jul 2016 | chronic obstructive pulmonary disease | AstraZeneca | Completed | Missed primary |
| Phase 4 | NCT02574975 | Apr 2015 → May 2016 | asthma | Zhujiang Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT04520230 | Oct 2014 → Dec 2019 | chronic obstructive pulmonary disease | Tanta University | Completed | No outcome recorded |
| Phase 4 | NCT01853787 | Jul 2014 → Jun 2015 | chronic obstructive pulmonary disease | University of Milan | Completed | No outcome recorded |
| Phase 4 | NCT01892787 | Jul 2013 → Dec 2014 | asthma | University of Dundee | Completed | No outcome recorded |
| Phase 4 | NCT01845025 | May 2013 → May 2016 | chronic asthma | Novartis Pharmaceuticals | Terminated | No outcome recorded |
| Phase 4 | NCT01794780 | Feb 2013 → May 2015 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 4 | NCT01712854 | Mar → Sep 2012 | chronic obstructive pulmonary disease | Columbia University | Terminated | No outcome recorded |
| Phase 4 | NCT01471340 | Jan 2012 → Nov 2016 | asthma | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT01760304 | Jan → Jul 2012 | chronic obstructive pulmonary disease | Brigham and Women's Hospital | Terminated | Missed primary |
| Phase 4 | NCT01620099 | Nov 2011 → Apr 2014 | asthma | Università degli Studi di Ferrara | Completed | No outcome recorded |
| Phase 4 | NCT01466712 | Nov 2011 → Dec 2014 | pulmonary emphysema | KU Leuven | Unknown | No outcome recorded |
| Phase 4 | NCT01397890 | Jul 2011 → Jun 2013 | chronic obstructive pulmonary disease | AstraZeneca | Completed | Met primary |
| Phase 4 | NCT01344655 | Apr 2011 → Sep 2012 | chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 4 | NCT01329276 | Jun → Nov 2010 | chronic obstructive pulmonary disease | University Hospital, Antwerp | Completed | No outcome recorded |
| Phase 4 | NCT00997477 | Jun → Jul 2010 | asthma | Novartis Pharmaceuticals | Withdrawn | No outcome recorded |
| Phase 4 | NCT01070888 | Feb 2010 → Apr 2014 | exercise-induced bronchoconstriction | Boston Children's Hospital | Terminated | No outcome recorded |
| Phase 4 | NCT00914654 | Jul 2009 → Dec 2010 | asthma | Bispebjerg Hospital | Unknown | No outcome recorded |
| Phase 4 | NCT00939341 | Jul 2009 → Aug 2010 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT00901368 | May 2009 → Sep 2010 | asthma | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Phase 4 | NCT00910793 | Aug 2008 → Aug 2010 | asthma | Wilfried De Backer | Completed | No outcome recorded |
| Phase 4 | NCT00702325 | Jun 2008 → Sep 2009 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT00633776 | Mar 2008 → Jan 2009 | chronic bronchitis, pulmonary emphysema | University of California, Los Angeles | Withdrawn | No outcome recorded Stop: Business |
| Phase 4 | NCT00546234 | Nov 2007 → Jan 2014 | asthma | University of Alberta | Withdrawn | No outcome recorded Stop: Enrollment |
| Phase 4 | NCT01186653 | Oct 2007 → May 2010 | chronic obstructive pulmonary disease | Hull University Teaching Hospitals NHS Trust | Completed | No outcome recorded |
| Phase 4 | NCT00489853 | Jul 2007 → Aug 2008 | chronic obstructive pulmonary disease | AstraZeneca | Completed | Met primary |
| Phase 4 | NCT00561886 | Apr → Oct 2007 | chronic obstructive pulmonary disease | Johannes Gutenberg University Mainz | Completed | No outcome recorded |
| Phase 4 | NCT00379028 | Sep 2006 → Jul 2007 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT01089322 | Dec 2005 → Apr 2009 | asthma | Rafael Stelmach | Completed | No outcome recorded |
| Phase 4 | NCT00139932 | Sep 2005 → Nov 2006 | chronic obstructive pulmonary disease | Merck Sharp & Dohme LLC | Completed | Met primary |
| Phase 4 | NCT00134979 | Oct 2004 → Nov 2005 | chronic obstructive pulmonary disease | Novartis Pharmaceuticals | Completed | Met primary |
| Phase 4 | NCT00272753 | Apr 2004 → Nov 2005 | asthma | AstraZeneca | Completed | No outcome recorded |
| Phase 4 | NCT00327353 | Jan 2004 → ? | asthma | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 4 | NCT00239421 | Nov 2003 → Sep 2004 | chronic obstructive pulmonary disease | Boehringer Ingelheim | Completed | Met primary |
| Phase 4 | NCT00490243 | Jul 2003 → Oct 2006 | asthma | Medical University of Lodz | Completed | No outcome recorded |
| Phase 4 | NCT00479739 | Nov 2002 → Jul 2004 | asthma | GlaxoSmithKline | Completed | Met primary |
| Phase not applicable15 trials · 1 met primary | ||||||
| — | NCT07595796 | Jun 2026 → Feb 2028 expected | — | Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University | Not yet recruiting | No outcome recorded |
| — | NCT06865040 | Jul 2025 → Mar 2028 expected | — | Centre Hospitalier Universitaire, Amiens | Recruiting | No outcome recorded |
| — | NCT07232264 | Mar → Sep 2025 | asthma | Bugra Kerget | Completed | No outcome recorded |
| — | NCT06597682 | Mar 2025 → Jul 2027 expected | long COVID-19 | Huashan Hospital | Not yet recruiting | No outcome recorded |
| — | NCT06105671 | Jan → Jul 2024 | — | Morten Hostrup, PhD | Completed | No outcome recorded |
| — | NCT05888350 | Apr 2023 → Apr 2025 | — | The First Affiliated Hospital of Guangzhou Medical University | Completed | No outcome recorded |
| — | NCT05553184 | Jul 2022 → May 2023 | obesity disorder, type 2 diabetes mellitus | University of Sherbrooke | Completed | No outcome recorded |
| — | NCT04616261 | Nov 2020 → Nov 2022 | — | University of Copenhagen | Unknown | No outcome recorded |
| — | NCT04137029 | Apr 2019 → Jul 2020 | reactive airway disease | Federal State Budgetary Institution, Pulmonology Scientific Research Institute | Unknown | No outcome recorded |
| — | NCT03565302 | Jun 2018 → May 2021 | hypertrophia musculorum vera | Morten Hostrup, PhD | Unknown | No outcome recorded |
| — | NCT02415179 | May 2015 → Feb 2016 | asthma | Mahidol University | Completed | No outcome recorded |
| — | NCT01457716 | Oct → Nov 2011 | — | Orion Corporation, Orion Pharma | Completed | No outcome recorded |
| — | NCT01194479 | Aug 2010 → Aug 2014 | type 1 diabetes mellitus | Yale University | Completed | No outcome recorded |
| — | NCT00159263 | Nov 2004 → Nov 2006 | asthma | Imperial College London | Completed | Met primary |
| — | NCT00728715 | Jan 2004 → Jan 2005 | bronchiectasis | Hospital General de Requena | Completed | No outcome recorded |
| Comparator or background therapy144 trials | ||||||
| Phase 0 | NCT01257048 Comparator | Aug 2011 → Jun 2012 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT06297668 Comparator | Apr → Jun 2024 | chronic obstructive pulmonary disease | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT02934607 Comparator | Nov 2016 → Mar 2017 | — | AstraZeneca | Completed | No outcome recorded |
| Phase 1 | NCT02403713 Comparator | Aug → Oct 2014 | asthma | Mundipharma Research Limited | Completed | No outcome recorded |
| Phase 1 | NCT02287272 Comparator | May → Jul 2014 | chronic obstructive pulmonary disease | Chiesi Farmaceutici S.p.A. | Completed | No outcome recorded |
| Show all 144 trials opens the full record — a long page | ||||||
News releases announcing trial results or a regulatory action · 33
| Date | Issuer | Release |
|---|---|---|
| 2026-09-23 | AstraZeneca | Regulatory Trixeo approved in the EU for the maintenance treatment of asthma astrazeneca.com ↗
Trixeo is the first and only triple-combination therapy approved in the EU for patients 12 years and older, independent of exacerbation history |
| 2026-09-03 | Chiesi Farmaceutici S.p.A. | Regulatory Chiesi advances its Carbon Minimal Inhaler journey as European submissions for its Single Inhaler Triple Therapy (SITT) and ICS/LABA combination next-generation propellant pMDIs are validated chiesi.com ↗
Regulatory submissions for next-generation propellant pMDIs (pressurized metered-dose inhalers) across Chiesi’s Single Inhaler Triple Therapy (SITT; or ICS/LABA/LAMA) and fixed double ICS/LABA combination (inhaled corticosteroid with a long-acting bronchodilator) range have been validated by Regulatory Agencies in Europe. |
| 2026-07-31 | Chiesi Farmaceutici S.p.A. | Regulatory Chiesi receives European Marketing Authorisation for its Single Inhaler Triple Therapy delivered via NEXThaler® for the maintenance treatment of Asthma chiesi.com ↗
The EC approval follows the positive opinion adopted by the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency in May 2026. |
| 2025-11-26 | Chiesi Farmaceutici S.p.A. | Results Chiesi Advanced Carbon Minimal Inhaler (CMI) Program with New Therapeutic Equivalence Data Presented at British Thoracic Society (BTS) Winter Meeting chiesi.com ↗
The two studies presented at BTS demonstrated therapeutic equivalence and similar safety profiles of Chiesi’s beclometasone dipropionate/ formoterol fumarate product formulated with next generation HFA-152a propellant, compared to the current HFA-134a formulation, in two different strengths 1 . |
| 2025-05-12 | AstraZeneca | Regulatory Trixeo Aerosphere approved in the UK as first inhaled respiratory medicine using next-generation propellant with near-zero Global Warming Potential astrazeneca.com ↗ |
| 2025-05-02 | AstraZeneca | Results Breztri met primary endpoints in KALOS and LOGOS Phase III trials in asthma astrazeneca.com ↗
Positive high-level results from the Phase III KALOS and LOGOS trials in patients with uncontrolled asthma showed that AstraZeneca’s fixed-dose triple-combination therapy Breztri Aerosphere (budesonide/glycopyrronium/formoterol fumarate or BGF (320/28.8/9.6μg)) met all primary endpoints |
| 2022-08-24 | Lupin Limited | Regulatory Lupin Receives Approval from U.S. FDA for Formoterol Fumarate Inhalation Solution lupin.com ↗ |
| 2022-03-29 | Respira Therapeutics, Inc. | Results Accessorized DPI: a Shortcut Towards Flexibility and Patient Adaptability in Dry Powder Inhalation. respiratherapeutics.com ↗
Two novel findings emerged from the data collected: the aerosol quality, measured as fine particle dose, was increased by adding the accessory promoting the formulation de agglomeration and the flow dependence of the aerosol formation was reduced [1]. |
| 2022-03-16 | Pfizer's Upjohn has merged with Mylan to form Viatris Inc. | Regulatory Viatris Inc. Announces Receipt of the First FDA Approval for Generic Version of Symbicort® Inhalation Aerosol, Breyna™ (Budesonide and Formoterol Fumarate Dihydrate Inhalation Aerosol), in Partnership with Kindeva viatris.com ↗
The FDA final approval of Breyna, the first FDA-approved generic version of Symbicort, is an exciting milestone both for our company and the many patients living with asthma and COPD. |
| 2021-11-01 | Alembic Pharmaceuticals Ltd. | Regulatory 23rd November, 2021, Vadodara, India alembicpharmaceuticals.com ↗
Alembic Pharmaceuticals Limited (Alembic) today announced that it has received final approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Formoterol Fumarate Inhalation Solution, 20 mcg/2 ml per Unit-Dose Vial. |
| 2021-03-08 | Pfizer's Upjohn has merged with Mylan to form Viatris Inc. | Regulatory Viatris Inc. and Kindeva Drug Delivery Announce FDA Tentative Approval of the First Abbreviated New Drug Application Generic Version of Symbicort® (budesonide/formoterol fumarate dihydrate) Inhalation Aerosol viatris.com ↗
today announced that the U.S. Food and Drug Administration (FDA) granted tentative approval of budesonide/formoterol fumarate dihydrate products, the first generic version of Symbicort ® based on an Abbreviated New Drug Application (ANDA). |
| 2019-06-19 | AstraZeneca | Regulatory Bevespi Aerosphere approved by the Japanese Ministry of Health, Labour and Welfare for patients with chronic obstructive pulmonary disease astrazeneca.com ↗
AstraZeneca today announced that Bevespi Aerosphere (glycopyrronium/formoterol fumarate) has been approved in Japan as a fixed-dose, long-acting dual bronchodilator to relieve symptoms in patients with chronic obstructive pulmonary disease (COPD). |
| 2018-12-20 | AstraZeneca | Regulatory Bevespi Aerosphere approved in the EU for chronic obstructive pulmonary disease astrazeneca.com ↗
AstraZeneca today announced that the European Commission (EC) has approved Bevespi Aerosphere (glycopyrronium/formoterol fumarate) in a pressurised metered-dose inhaler (pMDI) as a maintenance dual bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (COPD). |
| 2018-09-13 | AstraZeneca | Results AstraZeneca to present Fasenra long-term safety and efficacy data at European Respiratory Society International Congress 2018 astrazeneca.com ↗
Adding budesonide to formoterol reduces risk of clinically important deteriorations (CID) in moderate to very severe COPD |
| 2018-08-23 | AstraZeneca | Results AstraZeneca provides update on AERISTO Phase IIIb trial for Bevespi Aerosphere in chronic obstructive pulmonary disease astrazeneca.com ↗
AstraZeneca today announced top-line results from the AERISTO Phase IIIb trial for Bevespi Aerosphere (glycopyrronium/formoterol fumarate) in patients with moderate to very severe chronic obstructive pulmonary disease (COPD). |
| 2017-09-07 | AstraZeneca | Results Duaklir significantly improves lung function in COPD patients astrazeneca.com ↗
These results demonstrate the improvement in lung function achieved by the combination of aclidinium and formoterol compared to single LAMA bronchodilators tiotropium and aclidinium, with comparable safety. |
| 2017-09-07 | Niox | Results Circassia Announces Duaklir® Successfully Met Primary Endpoints in AMPLIFY Phase III Study in Chronic Obstructive Pulmonary Disease niox.com ↗
The AMPLIFY study met its co-primary efficacy endpoints with Duaklir® demonstrating statistically significant and clinically meaningfully improvements in lung function, measured by forced expiratory volume in one second (FEV1), compared with the combination’s individual component monotherapies (aclidinium and formoterol). |
| 2017-05-22 | Merck Sharp & Dohme LLC | Results Merck Announces Top-Line Results from the Long Term LABA Safety Study of DULERA (mometasone furoate and formoterol fumarate dihydrate) Inhalation Aerosol merck.com ↗
We are pleased this study met both its primary safety and key secondary efficacy endpoints, |
| 2017-05-18 | AstraZeneca | Results AstraZeneca to present scientific advancements from growing respiratory portfolio at the American Thoracic Society conference 2017 astrazeneca.com ↗ |
| 2016-09-06 | GlaxoSmithKline | Results GSK presents positive results from phase III FULFIL study of closed triple combination therapy FF/UMEC/VI versus Symbicort® Turbohaler® in COPD at ERS International Congress gsk.com ↗
In addition, the proportion of patients who responded with the minimum clinically important difference in SGRQ (-4 units) was 50% on closed triple and 41% on budesonide/formoterol (odds ratio 1.41; p<0.001). |
| 2016-08-30 | AstraZeneca | Results AstraZeneca to present new data highlighting its growing respiratory portfolio and pipeline at European Respiratory Society 2016 astrazeneca.com ↗
A Duaklir (aclidinium/formoterol) study showing reduced deterioration in COPD compared to monotherapies and placebo (abstract #PA301) |
| 2016-06-20 | GlaxoSmithKline | Results FULFIL study shows superiority of closed triple combination therapy FF/UMEC/VI versus Symbicort® Turbohaler® in improving lung function and health-related quality of life in COPD patients gsk.com ↗ |
| 2016-04-25 | AstraZeneca | Regulatory Bevespi Aerosphere™ approved by the US FDA for patients with COPD astrazeneca.com ↗ |
| 2015-05-19 | GlaxoSmithKline | Results GSK presents data at ATS on the role of blood eosinophil levels as a potential biomarker in the treatment of COPD gsk.com ↗
GSK today presented two abstracts at the American Thoracic Society (ATS) meeting that provide data on the role of blood eosinophils as a potential biomarker to determine responsiveness to treatment with an inhaled corticosteroid (ICS) in patients with COPD. |
| 2015-03-18 | AstraZeneca | Results AstraZeneca announces positive Phase III top-line results for PT003 from PINNACLE 1 and PINNACLE 2 studies in COPD astrazeneca.com ↗
Both PT001 and PT005 also demonstrated statistically significant improvements in trough FEV1 compared to placebo. |
| 2014-04-29 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Receives European Marketing Authorization for DuoResp Spiromax® for the Treatment of Asthma and COPD tevapharm.com ↗
Teva Pharmaceutical Industries Ltd., (NYSE:TEVA) announced today that the European Commission has granted marketing authorization for DuoResp Spiromax® for the treatment of patients with asthma and chronic obstructive pulmonary disease (COPD) where the use of a combination of an inhaled corticosteroid and long-acting beta2-adrenoceptor agonist is appropriate. |
| 2014-04-14 | Orion Corporation, Orion Pharma | Regulatory Orion receives first marketing authorisations for Bufomix Easyhaler® product orionpharma.com ↗
Orion Corporation has received Irish and Hungarian marketing authorisation for Bufomix Easyhaler®, an inhaled budesonide-formoterol combination product indicated for asthma and chronic obstructive pulmonary disease (COPD). |
| 2014-02-21 | Teva Branded Pharmaceutical Products R&D, Inc. | Regulatory Teva Receives CHMP Positive Opinion for DuoResp® Spiromax® for the Treatment of Patients Diagnosed with Asthma and COPD in Europe tevapharm.com ↗
This CHMP decision creates a path forward for a final approval decision from the European Commission that is expected in the next few months. |
| 2013-09-08 | Boehringer Ingelheim | Results Olodaterol Shows Sustained Improvements in Lung Function in Patients with Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD) prnewswire.com ↗ |
| 2013-03-21 | Orion Corporation, Orion Pharma | Regulatory Orion has submitted a marketing authorisation application for combined budesonide-formoterol formulation of the Easyhaler® product family orionpharma.com ↗
Orion Corporation has submitted a marketing authorisation application for combined budesonide-formoterol formulation of the Easyhaler® product family in Europe. |
| 2012-02-07 | Orion Corporation, Orion Pharma | Results Orion Group Financial Statement Release for 2011 orionpharma.com ↗
On 7 February Orion announced that study results received early in 2012 on a budesonide-formoterol formulation product under development for broadening the range of the Easyhaler® product family were promising, but yet insufficient for submission of an application for marketing authorisation. |
| 2012-02-07 | Orion Corporation, Orion Pharma | Results Orion continues development of inhalable budesonide-formoterol combined formulation orionpharma.com ↗
Study results received early in 2012 were promising, but yet insufficient for submission of an application for marketing authorisation. |
| 2011-10-24 | Merck Sharp & Dohme LLC | Results Merck Announces Presentation of Phase III Investigational Studies Evaluating DULERA® (mometasone furoate and formoterol fumarate dihydrate) Inhalation Aerosol in Chronic Obstructive Pulmonary Disease (COPD) merck.com ↗
In Study 2, DULERA 200 mcg/10 mcg and DULERA 400 mcg/10 mcg significantly improved AM predose FEV1 at Week 13 compared to treatment with placebo, but neither dose of DULERA reached statistical significance compared to treatment with formoterol 10 mcg. |
All press releases naming this drug 40 releases
Evidence & citations 31 cited values
Every value below carries the sentence it was read from. 425 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | formoterol | “This study investigated the efficacy and tolerability of a new asthma therapy combining fluticasone propionate and formoterol fumarate (fluticasone/formoterol)*, administered...” PMID 23870606 ↗ Jul 2013282“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 ↗ “Dual Therapy (LABA + LAMA): Patients receive a long-acting beta-agonist (LABA) such as Formoterol, Salmeterol, Olodaterol, Vilanterol, or Indacaterol, in combination with a...” NCT07058259 ↗ “In the first study period (Period 1), patients with moderate to severe persistent asthma according to GINA criteria, with or without COPD, will be randomized at a 1: 1 ratio to...” NCT04233190 ↗ “Relative Potency of Formoterol Novolizer® 12 µg Compared to Formoterol Aerolizer® 12 µg in Patients With Stable Asthma Using Bronchoprovocation With Methacholine as a Bioassay...” NCT01256086 ↗ “This study was conducted to evaluate the long-term safety of mometasone furoate/formoterol (MF/F) administered through metered-dose inhaler (MDI) in patients with persistent...” PMID 20874458 ↗ Nov 2010 “A U.S., multicenter, five-way crossover study compared single doses of formoterol, a long-acting beta-agonist, via pMDI (2.25, 4.5, and 9 micrograms) or dry powder inhaler (12...” PMID 24717790 ↗ Mar 2014 “160 ug budesonide and 4.5 ug formoterol fumarate dihydrate, administered as two inhalations (2 x Z7200 capsules) of budesonide 80 ug/inhalation and formoterol 2.25...” NCT02631941 ↗ “160 ug budesonide and 4.5 ug formoterol fumarate dihydrate, administered as two inhalations (2 x Z7200 capsules) of budesonide 80 ug/inhalation and formoterol 2.25...” NCT02237508 ↗ “Primary objectives were to assess total systemic exposure (without charcoal) and lung exposure (with charcoal) of budesonide, glycopyrronium, and formoterol administered as BGF...” PMID 32253054 ↗ Apr 2020 “We evaluated the effects of the long acting bronchodilator components of the extrafine single inhaler triple therapy beclometasone dipropionate/formoterol/glycopyrronium...” PMID 33298062 ↗ Dec 2020 |
| Known as | Atimos | “Thus, the primary objective for the present study is to compare the two extremes of available long acting beta-agonist formulations - i.e. extra fine HFA formoterol ( Atimos )...” NCT01892787 ↗2“BDP 100 µg pMDI, 4 puffs (Qvar®, total dose: BDP 400 µg) + formoterol fumarate 6 µg pMDI, 4 puffs (Atimos®, total dose: formoterol 24 µg)” NCT01803087 ↗ “Formoterol 12 μg pMDI (Atimos®)” NCT01344655 ↗ |
| Known as | CHF 1531 | “different doses of CHF 1531 pressurized metered dose inhaler (pMDI) containing formoterol fumarate” NCT03086460 ↗ |
| Known as | F12D | “Formoterol fumarate 12 μg DPI (F12D)” NCT00746330 ↗ |
| Known as | F12M | “Formoterol fumarate 12 μg pMDI (F12M)” NCT00746330 ↗ |
| Known as | FF | ClinicalTrials.gov intervention name — accepted as the source's own label NCT05898984 ↗ |
| Known as | FF MDI | “Patients received GFF MDI 18/9.6 μg, glycopyrrolate (GP) MDI 18 μg, formoterol fumarate (FF) MDI 9.6 μg, or placebo MDI, twice-daily for 24 weeks.” PMID 32450869 ↗ May 20201“Formoterol Fumarate Metered Dose Inhaler (FF MDI; PT005); Formoterol Fumarate Inhalation Aerosol administered as 2 inhalations twice-daily (BID)” NCT02343458 ↗ |
| Known as | FFIS | “nebulized formoterol fumarate inhalation solution (Perforomist**, FFIS 20g BID)” PMID 19232039 ↗ Mar 2009 |
| Known as | FOR | “twice-daily inhaled corticosteroid/long-acting β2-agonist therapy [budesonide/formoterol (BUD/FOR)] 400 µg/12 µg in patients with symptomatic COPD at risk of exacerbations” PMID 29313286 ↗ Jan 20182“extrafine beclomethasone dipropionate/formoterol fumarate (BDP/FOR), 100/6 μg pMDI, 2 inhalations BID, vs. FOR 12 μg pMDI, 1 inhalation BID” PMID 24953015 ↗ Jun 2014 “formoterol fumarate 12 microg twice-daily (FOR) plus TIO 18 microg once-daily” PMID 20580216 ↗ Jun 2010 |
| Known as | Foradil | “FORADIL® AEROLIZER® consists of a capsule dosage form containing a dry powder formulation of FORADIL (formoterol fumarate) intended for oral inhalation only with the AEROLIZER Inhaler.” NCT01108627 ↗10“plus foradil (12 mcg formoterol fumarate) supplied as dry powder in size-2 capsules and administered as a single dose via C2S inhaler.” NCT00801684 ↗ “fluticasone plus formoterol (Flixotide Evohaler, pMDI, Flovent [HFA]; Foradil, DPI, Foradil Aerolizer) administered concurrently” PMID 23368897 ↗ Feb 2013 “long acting bronchodilators "foradil/spiriva" or combined LABD and inhaled steroids” NCT02257463 ↗ “Formoterol (Foradil®) 12 micrograms administered through Aerolizer®.” NCT00460577 ↗ “Foradil inh kap 12 mcg/dosage, 60 caps” NCT00628758 ↗ |
| Known as | Foradil (aerosolizer dry powder formoterol fumarate) | “Foradil (aerosolizer dry powder formoterol fumarate)” NCT00633776 ↗ |
| Known as | Foradil Aerolizer | “FORADIL® AEROLIZER® consists of a capsule dosage form containing a dry powder formulation of FORADIL (formoterol fumarate) intended for oral inhalation only with the AEROLIZER Inhaler.” NCT01108627 ↗6“received nebulized formoterol fumarate (Perforomist inhalation solution; FFIS 20 microg) or DPI (Foradil Aerolizer; FA 12 microg), or placebo twice daily for 12 weeks.” PMID 18363201 ↗ Feb 2008 “fluticasone plus formoterol (Flixotide Evohaler, pMDI, Flovent [HFA]; Foradil, DPI, Foradil Aerolizer) administered concurrently” PMID 23368897 ↗ Feb 2013 “1 or 2 doses of formoterol, (Foradil Aerolizer 12 mcg/capsule) a long-acting bronchodilator” NCT00643578 ↗ “Foradil Aerolizer 12 ug (One inhalation of formoterol 12 ug)” NCT00830102 ↗ “Drug: Formoterol Fumarate 12 mcg (Foradil Aerolizer)” NCT06865040 ↗ “Formoterol Fumarate 12 μg (Foradil® Aerolizer®)” NCT01085045 ↗ |
| Known as | Form | “The participants were then randomized to budesonide/formoterol (Bud + Form; 400/12 μg BID), fluticasone/salmeterol (Flu + Salm; 250/50 μg BID), or formoterol only (12 μg BID)...” PMID 34464242 ↗ Nov 20211“Many studies have shown the superior efficacy of budesonide (BUD)/formoterol (FORM) maintenance and reliever therapy, but still lack evidence of its efficacy in Chinese asthma patients” PMID 22932169 ↗ Sep 2012 |
| Known as | formoterol (fumarate dihydrate) | “GFF MDI is a long-acting muscarinic antagonist/long-acting β2-agonist fixed-dose combination of glycopyrronium (GP) and formoterol fumarate dihydrate (FF), delivered by a...” PMID 30218695 ↗ Sep 20185“Extrafine beclomethasone dipropionate 100 mcg/formoterol fumarate dihydrate 6 mcg (Foster®), 1 inhalation twice daily for 4 weeks, plus salbutamol 100 mcg as needed (max 200...” NCT07809555 ↗ “formoterol (fumarate dihydrate) 12 microg - beclomethasone (dipropionate) 200 microg administered BID, per inhalation using '100/6' Metered Dose Inhaler” NCT03846570 ↗ “Symbicort Turbohaler (Budesonide and Formoterol Fumarate Dihydrate) without Turbo+ for three months.” NCT03788395 ↗ |
| Known as | Formoterol (Pressair) | “Formoterol (Pressair®)” NCT02796651 ↗ |
| Known as | formoterol fumarate | “BACKGROUND: This study evaluated the lung deposition and the distribution pattern in the airways of a fixed combination of beclometasone dipropionate (BDP) and formoterol...” PMID 29989511 ↗ Jul 2018143“The purpose of this study was to assess whether the risk of serious asthma-related events (asthma-related hospitalizations, asthma related intubations, and asthma related...” NCT01845025 ↗ “Glycopyrrolate/formoterol fumarate (GFF) metered dose inhaler (MDI) is a fixed-dose combination of the long-acting muscarinic antagonist (LAMA), glycopyrrolate (GP), and the...” PMID 29567116 ↗ Feb 2018 “Eligible participants were randomized 1:1 to receive either extrafine beclomethasone dipropionate/formoterol fumarate (100 mcg/6 mcg, 1 puff twice daily) plus as-needed...” NCT07809555 ↗ “An extrafine combination of beclometasone dipropionate (BDP) and formoterol fumarate (FF) via a pressurised metered-dose inhaler (pMDI) has been commercially available for some...” PMID 28065679 ↗ Jan 2017 “Each subject will receive SKP FlutiForm HFA pMDI 250/10 microgram twice daily for 60 weeks (two actuations of SKP FlutiForm HFA pMDI 125/5 microgram/actuation) for a total...” NCT00747318 ↗ “The inhaled corticosteroid (ICS) fluticasone propionate (fluticasone) and the long-acting β2-agonist (LABA) formoterol fumarate (formoterol) are being made available as a...” PMID 21605396 ↗ May 2011 “The purpose of this study is to evaluate the safety and efficacy of inhaled formoterol fumarate (7.2 and 9.6 µg ex-actuator) compared to placebo and Foradil Aerolizer in...” NCT01043601 ↗ “Foster is a combination therapy containing beclometasone dipropionate (an inhaled corticosteroid, or ICS) and formoterol fumarate (a long-acting beta-agonist, or LABA), which...” NCT06869382 ↗ “formoterol fumarate, a long-acting β2-AR agonist given four hours following injury, when glomerular dysfunction is already established, restored glomerular structure,...” NCT07022418 ↗ “BGF 160 (Breztri Aerosphere™ in USA, Trixeo™ in France) Inhalation aerosol: pressurized metered dose inhaler containing a combination of budesonide (160 mcg), glycopyrrolate (9...” NCT06110403 ↗ |
| Known as | formoterol fumarate dehydrate | “SPIROMAX (BF) Budesonide and formoterol fumarate dehydrate (160/4.5 and 320/9 μg)” NCT02062463 ↗1“Budesonide 160 mcg/Glycopyrrolate 7.2 mcg/Formoterol fumarate dehydrate 5 mcg” NCT06531798 ↗ |
| Known as | Formoterol Fumarate Inhalation Aerosol | “Formoterol Fumarate Inhalation Aerosol” NCT02766608 ↗ |
| Known as | formoterol fumarate metered dose inhaler (FF MDI) | “formoterol fumarate metered dose inhaler (FF MDI)” NCT01854658 ↗ |
| Known as | Formoterol Furamate | “The Investigational Medicinal Product (IMP) consists of a combination of Budesonide (corticosteroid) and Formoterol Furamate (fast-acting β2 agonist) dihydrate.” NCT06429475 ↗ |
| Known as | FORMOTEROL VIATRIS | “FORMOTEROL FUMARATE 12 µg pwd inhalation capsule (FORMOTEROL VIATRIS®)” NCT06865040 ↗ |
| Known as | Oxeze | “Oxeze” NCT00546234 ↗ |
| Known as | Oxis | “Oxis turbuhaler 4.5-9 mcg/dosage, 60 dosage” NCT00628758 ↗ |
| Known as | Oxis Turbuhaler | “Formoterol (Oxis Turbuhaler®, AstraZeneca), 4.5μg/ dose, 60 inhalations.” NCT01836016 ↗2“Oral Prednisolone + Formoterol (Oxis® Turbuhaler) During Two Weeks” NCT00259779 ↗ “Formoterol Alone (Oxis® Turbuhaler® 4.5 µg)” NCT00288379 ↗ |
| Known as | Perforomist | “Nebulized Formoterol Fumarate (PERFOROMIST®) Administered in Sequence and as a Combined Solution” NCT03573817 ↗2“nebulized formoterol fumarate inhalation solution (Perforomist**, FFIS 20g BID)” PMID 19232039 ↗ Mar 2009 “Revefenacin (YUPELRI) & Formoterol (Perforomist)” NCT04655170 ↗ |
| Known as | Perforomist (nebulized formoterol fumarate) | “Perforomist (nebulized formoterol fumarate)” NCT00633776 ↗ |
| Known as | Perforomist inhalation solution | “received nebulized formoterol fumarate (Perforomist inhalation solution; FFIS 20 microg) or DPI (Foradil Aerolizer; FA 12 microg), or placebo twice daily for 12 weeks.” PMID 18363201 ↗ Feb 2008 |
| Known as | PT005 | “Formoterol Fumarate Metered Dose Inhaler (FF MDI; PT005); Formoterol Fumarate Inhalation Aerosol administered as 2 inhalations twice-daily (BID)” NCT02343458 ↗3“Budesonide (BD; PT008) and formoterol fumarate (FF; PT005) in a metered-dose inhaler (MDI); (BFF MDI; PT009)” NCT02196077 ↗ “Formoterol Fumarate MDI (PT005; 7.2 and 9.6 µg Ex-actuator)” NCT01043601 ↗ “FF MDI (PT005)” NCT01970878 ↗ |
| Action | Activate | “long-acting β(2)-adrenergic agonists” PMID 22383665 ↗ Aug 2012 |
| Modality | Other / unclassified | “long-acting β(2)-adrenergic agonists” PMID 22383665 ↗ Aug 2012 |
| Route | Inhaled | “Formoterol Inhalant Powder” NCT00159263 ↗ |