Mometasone furoate
Regulatory milestones approvals, filings & regulatory actions · 16 recorded
| Milestone | Jurisdiction | Brand | Indication | Date | Sentence it was read from |
|---|---|---|---|---|---|
| Filed asthma 1 milestone | |||||
| Filed | EU (EMA) | — | asthma | — | “The regulatory submissions for IND/MF and IND/GLY/MF have recently been accepted for review by the European Medicines Agency (EMA).” novartis.com ↗ |
| Filed chronic obstructive pulmonary disease 1 milestone | |||||
| Filed | US (FDA) | DULERA | chronic obstructive pulmonary disease | 2011-07-29 | “DULERA (mometasone furoate and formoterol fumarate dihydrate) for the treatment of chronic obstructive pulmonary disease (COPD) has been accepted for review by the FDA.” merck.com ↗ |
| Approved Indication not stated 7 milestones | |||||
| Approved | EU (EMA) | Atectura Breezhaler | — | 2020-05-30 | europa.eu ↗ |
| Label expansion | US (FDA) | SINUVA | — | 2020-04-28 | fda.gov ↗ |
| Label expansions (2) | US (FDA) | ASMANEX HFA | — | 2016-07-12 – 2019-08-12 | fda.gov ↗ |
| Label expansions (3) | US (FDA) | ELOCON | — | 1995-10-03 – 2013-04-19 | fda.gov ↗ |
| Label expansions (5) | US (FDA) | NASONEX | — | 1998-11-18 – 2011-01-19 | fda.gov ↗ |
| Label expansion | US (FDA) | ASMANEX TWISTHALER | — | 2008-02-01 | fda.gov ↗ |
| Approved | US (FDA) | ELOCON | — | 1987-04-30 | fda.gov ↗ |
Trials 105 · started per year
| Phase | Registry id | Dates | Indication | Sponsor | Status | Outcome |
|---|---|---|---|---|---|---|
| Phase 17 trials | ||||||
| Phase 1 | NCT05887843 | Jun → Sep 2023 | seasonal allergic rhinitis | Sandoz | Terminated | No outcome recorded Stop: Business |
| Phase 1 | NCT02967731 | Jun → Dec 2017 | chronic rhinosinusitis | Lyra Therapeutics | Completed | No outcome recorded |
| Phase 1 | NCT02973776 | Dec 2016 → Feb 2017 | psoriasis | LEO Pharma | Completed | No outcome recorded |
| Phase 1 | NCT01353599 | Aug 2011 → Mar 2016 | spinal cord injury | James J. Peters Veterans Affairs Medical Center | Unknown | No outcome recorded |
| Phase 1 | NCT00662883 | Nov 2007 → Feb 2008 | — | Javelin Pharmaceuticals | Completed | No outcome recorded |
| Phase 1 | NCT00544687 | Sep → Nov 2007 | — | Zalicus | Completed | No outcome recorded |
| Phase 1 | NCT00418509 | Nov 2006 → ? | — | Novartis | Completed | No outcome recorded |
| Phase 217 trials · 3 met primary · 1 missed | ||||||
| Phase 2 | NCT06126952 | Oct 2023 → Feb 2024 | seasonal allergic rhinitis | MEDA Pharma GmbH & Co. KG | Completed | No outcome recorded |
| Phase 2 | NCT05505214 | Sep 2023 → Sep 2025 | radiodermatitis | Montefiore Medical Center | Withdrawn | No outcome recorded |
| Phase 2 | NCT05035654 | Nov 2021 → Aug 2023 | chronic rhinosinusitis | Lyra Therapeutics | Completed | No outcome recorded |
| Phase 2 | NCT04849390 | Jun 2021 → Oct 2023 | eosinophilic esophagitis | EsoCap AG | Completed | Met primary |
| Phase 2 | NCT04589663 | Jun 2021 → Apr 2022 | asthma | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT04041609 | May 2019 → Mar 2020 | chronic rhinosinusitis | Lyra Therapeutics | Completed | Missed primary |
| Phase 2 | NCT04179461 | Mar 2018 → Oct 2019 | childhood onset asthma | Children's Hospital Medical Center, Cincinnati | Completed | No outcome recorded |
| Phase 2 | NCT02113267 | Apr 2014 → Sep 2018 | eosinophilic esophagitis | Mogens Bove | Terminated | No outcome recorded Stop: Enrollment |
| Phase 2 | NCT02061202 | Mar 2014 → Nov 2017 | sickle cell disease | Jeffrey Glassberg | Completed | No outcome recorded |
| Phase 2 | NCT01894503 | Jun → Oct 2013 | chronic rhinosinusitis | Intersect ENT | Completed | No outcome recorded |
| Phase 2 | NCT01615874 | Jan → Sep 2013 | asthma | Organon and Co | Withdrawn | No outcome recorded |
| Phase 2 | NCT01555151 | Jul 2012 → Jul 2013 | asthma | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT01502371 | Jan 2012 → Jan 2015 | asthma | Organon and Co | Completed | Met primary |
| Phase 2 | NCT00845481 | Jan → Mar 2009 | psoriasis | LEO Pharma | Completed | No outcome recorded |
| Phase 2 | NCT00635882 | Feb 2008 → Jun 2009 | asthma | Organon and Co | Completed | Met primary |
| Phase 2 | NCT00557739 | Nov 2007 → Jan 2008 | psoriasis | Zalicus | Completed | No outcome recorded |
| Phase 2 | NCT00779545 | Apr → Aug 2004 | perennial allergic rhinitis | Organon and Co | Completed | No outcome recorded |
| Phase 2/31 trial · 1 missed | ||||||
| Phase 2/3 | NCT01732536 | Jan → Nov 2013 | chronic rhinosinusitis, nasal cavity polyp | Intersect ENT | Completed | Missed primary |
| Phase 345 trials · 21 met primary · 8 missed | ||||||
| Phase 3 | NCT05776927 | Aug 2026 → Dec 2028 expected | asthma | Novartis Pharmaceuticals | Recruiting | No outcome recorded |
| Phase 3 | NCT05295459 | May 2022 → Apr 2025 | chronic rhinosinusitis | Lyra Therapeutics | Completed | No outcome recorded |
| Phase 3 | NCT05219968 | Jan 2022 → Mar 2024 | chronic rhinosinusitis | Lyra Therapeutics | Completed | Missed primary |
| Phase 3 | NCT04484493 | Aug → Oct 2020 | COVID-19, anosmia | Benha University | Completed | Missed primary |
| Phase 3 | NCT03358329 | Nov 2017 → Jan 2019 | chronic rhinosinusitis, polyp of ethmoidal sinus | Intersect ENT | Completed | No outcome recorded |
| Phase 3 | NCT02892344 | Jan 2017 → Nov 2018 | asthma | Novartis Pharmaceuticals | Completed | Met primary |
| Phase 3 | NCT02870205 | Aug 2016 → Jan 2017 | seasonal allergic rhinitis | Glenmark Specialty S.A. | Completed | Met primary |
| Phase 3 | NCT02741271 | May 2016 → Dec 2017 | asthma | Organon and Co | Completed | Met primary |
| Phase 3 | NCT02631551 | Mar → Jul 2016 | seasonal allergic rhinitis | Glenmark Specialty S.A. | Completed | Met primary |
| Phase 3 | NCT02571777 | Dec 2015 → Jun 2019 | asthma | Novartis Pharmaceuticals | Completed | Met primary |
| Phase 3 | NCT02291549 | Dec 2014 → Oct 2016 | chronic rhinosinusitis, polyp of ethmoidal sinus | Intersect ENT | Completed | Met primary |
| Phase 3 | NCT02125253 | Jan → Mar 2014 | seasonal allergic rhinitis | Amneal Pharmaceuticals, LLC | Completed | No outcome recorded |
| Phase 3 | NCT01702103 | Oct 2012 → Jan 2013 | Achoo syndrome, nasal disorder | PH&T S.p.A. | Unknown | No outcome recorded |
| Phase 3 | NCT01386125 | Jun 2011 → Feb 2013 | nasal cavity polyp | Organon and Co | Completed | Met primary |
| Phase 3 | NCT01135134 | Jun → Oct 2010 | perennial allergic rhinitis | Organon and Co | Completed | Met primary |
| Phase 3 | NCT01165424 | Apr → Dec 2010 | perennial allergic rhinitis | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT01038427 | Dec 2009 → Feb 2010 | seasonal allergic rhinitis | Sandoz | Completed | No outcome recorded |
| Phase 3 | NCT00732381 | Aug → Nov 2008 | seasonal allergic rhinitis | Organon and Co | Completed | Met primary |
| Phase 3 | NCT00728416 | Aug → Oct 2008 | allergic rhinitis | Organon and Co | Completed | Met primary |
| Phase 3 | NCT00733005 | Jul → Oct 2008 | allergic rhinitis | Organon and Co | Completed | Missed primary |
| Phase 3 | NCT00599027 | May 2008 → May 2009 | allergic rhinitis, asthma | Organon and Co | Completed | Met primary |
| Phase 3 | NCT00552032 | Aug 2007 → Jan 2010 | adenoid hypertrophy | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00438659 | Aug 2007 → Jan 2010 | breast cancer, radiodermatitis, toxic dermatosis | North Central Cancer Treatment Group | Completed | Missed primary |
| Phase 3 | NCT00442117 | Jun 2007 → Jul 2009 | asthma | Organon and Co | Completed | Missed primary |
| Phase 3 | NCT00424008 | Apr 2007 → Nov 2008 | asthma | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00453063 | Mar → Jun 2007 | seasonal allergic rhinitis | Organon and Co | Completed | Mixed |
| Phase 3 | NCT00468312 | Mar → Jul 2007 | seasonal allergic rhinitis | Organon and Co | Completed | Met primary |
| Phase 3 | NCT00720382 | Mar 2007 → Jun 2008 | perennial allergic rhinitis | Meda Pharmaceuticals | Completed | No outcome recorded |
| Phase 3 | NCT00423176 | Dec 2006 → Jun 2008 | sinusitis | Organon and Co | Terminated | Missed primary Stop: Business |
| Phase 3 | NCT00383435 | Oct 2006 → Jul 2010 | chronic obstructive pulmonary disease | Organon and Co | Completed | Met primary |
| Phase 3 | NCT00383240 | Sep 2006 → Sep 2008 | asthma | Organon and Co | Completed | Met primary |
| Phase 3 | NCT00383552 | Sep 2006 → Aug 2008 | asthma | Organon and Co | Completed | Met primary |
| Phase 3 | NCT00383721 | Sep 2006 → Jul 2010 | chronic obstructive pulmonary disease | Organon and Co | Completed | Mixed |
| Phase 3 | NCT00381485 | Jul 2006 → Jan 2008 | asthma | Organon and Co | Completed | Met primary |
| Phase 3 | NCT00378378 | Jul 2006 → Jun 2008 | nasal cavity polyp | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00379288 | Jun 2006 → Nov 2007 | asthma | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00224523 | Sep 2005 → Feb 2007 | perennial allergic rhinitis | GlaxoSmithKline | Completed | No outcome recorded |
| Phase 3 | NCT00783224 | Sep → Nov 2005 | perennial allergic rhinitis | Organon and Co | Completed | Missed primary |
| Phase 3 | NCT00732368 | May 2005 → Jan 2006 | perennial allergic rhinitis | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00731185 | Sep 2003 → Sep 2005 | nasal cavity polyp | Organon and Co | Completed | Met primary |
| Phase 3 | NCT03879772 | Mar → Jul 1996 | seasonal allergic rhinitis | Organon and Co | Completed | Met primary |
| Phase 3 | NCT03855228 | Mar → Aug 1995 | allergic rhinitis | Organon and Co | Completed | Missed primary |
| Phase 3 | NCT03882047 | Aug → Sep 1994 | seasonal allergic rhinitis | Organon and Co | Completed | Met primary |
| Phase 3 | NCT03861559 | Mar → Jun 1994 | seasonal allergic rhinitis | Organon and Co | Completed | Met primary |
| Phase 3 | NCT03855189 | Aug → Oct 1993 | seasonal allergic rhinitis | Organon and Co | Completed | Met primary |
| Phase 430 trials · 2 met primary · 6 missed | ||||||
| Phase 4 | NCT07696806 | Jul 2026 → Jun 2027 expected | hyperpigmentation of the skin | Sameh Sarsik | Enrolling by invitation | No outcome recorded |
| Phase 4 | NCT07593898 | Jan 2025 → Jan 2026 | allergic rhinitis | Dr. Behcet Uz Children's Hospital | Completed | No outcome recorded |
| Phase 4 | NCT06399783 | Oct 2024 → Oct 2027 expected | alopecia areata | Assiut University | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT05382494 | Dec 2022 → Jul 2025 | obstructive sleep apnea syndrome, otorhinolaryngologic disease | Murdoch Childrens Research Institute | Completed | Missed primary |
| Phase 4 | NCT03141424 | Jun 2022 → Oct 2024 | asthma | Hvidovre University Hospital | Completed | No outcome recorded |
| Phase 4 | NCT05038202 | Jun 2021 → Apr 2024 | allergic rhinitis | Yingu Pharmaceutical Co., Ltd | Unknown | Met primary |
| Phase 4 | NCT04898764 | Oct 2020 → Apr 2025 | rhinitis | University Hospital, Ghent | Completed | No outcome recorded |
| Phase 4 | NCT03705793 | Jan 2019 → Feb 2020 | allergic rhinitis, chronic rhinosinusitis | Washington University School of Medicine | Completed | No outcome recorded |
| Phase 4 | NCT02668302 | Nov 2015 → Nov 2016 | chronic ethmoidal sinusitis | Collin County Ear Nose & Throat | Completed | Missed primary |
| Phase 4 | NCT02397915 | Mar → Jun 2015 | allergic rhinitis | GlaxoSmithKline | Completed | Met primary |
| Phase 4 | NCT02495064 | Jan 2015 → Dec 2016 | radiodermatitis | Yao Liao | Unknown | No outcome recorded |
| Phase 4 | NCT01997463 | Aug 2014 → Jun 2016 | childhood onset asthma | University of Arizona | Completed | Missed primary |
| Phase 4 | NCT02110654 | Jun 2014 → Nov 2020 | asthma, nasal cavity polyp, sinusitis | First Affiliated Hospital, Sun Yat-Sen University | Completed | No outcome recorded |
| Phase 4 | NCT02565212 | May → Oct 2014 | allergic rhinitis | Istanbul Training and Research Hospital | Completed | No outcome recorded |
| Phase 4 | NCT01616160 | Jul 2013 → Jan 2017 | nasal cavity polyp | Massachusetts General Hospital | Terminated | No outcome recorded Stop: Enrollment |
| Phase 4 | NCT01861145 | May 2013 → Dec 2015 | enuresis, obstructive sleep apnea syndrome | University of Alberta | Withdrawn | No outcome recorded Stop: Enrollment |
| Phase 4 | NCT01471340 | Jan 2012 → Nov 2016 | asthma | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT01635088 | Jun → Dec 2011 | asthma | California Allergy and Asthma Medical Group, Inc. | Completed | No outcome recorded |
| Phase 4 | NCT01098071 | Aug 2008 → Sep 2009 | adenoid hypertrophy | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT00521599 | May 2007 → Mar 2009 | asthma | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT00491504 | Feb → Jul 2007 | seasonal allergic rhinitis | Organon and Co | Completed | Missed primary |
| Phase 4 | NCT00687531 | Nov 2006 → Sep 2009 | asthma | Organon and Co | Terminated | No outcome recorded |
| Phase 4 | NCT00394355 | Sep 2006 → Oct 2009 | asthma | Organon and Co | Completed | Missed primary |
| Phase 4 | NCT00491374 | Sep 2006 → Oct 2007 | perennial allergic rhinitis | Schering-Plough | Terminated | No outcome recorded Stop: Enrollment |
| Phase 4 | NCT00359216 | May 2006 → Jan 2008 | obstructive sleep apnea syndrome, perennial allergic rhinitis | Organon and Co | Completed | Missed primary |
| Phase 4 | NCT00358527 | May → Oct 2006 | seasonal allergic rhinitis | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT00553891 | May 2006 → Oct 2009 | adenoid hypertrophy, nasal disorder | Organon and Co | Withdrawn | No outcome recorded Stop: Enrollment |
| Phase 4 | NCT00711165 | Aug 2005 → Apr 2006 | asthma | Creighton University | Completed | No outcome recorded |
| Phase 4 | NCT00236106 | Feb → Jun 2005 | atopic eczema | Children´s Clinic, Randers | Completed | No outcome recorded |
| Phase 4 | NCT00834119 | Sep 2003 → Apr 2004 | allergic rhinitis | Organon and Co | Completed | No outcome recorded |
| Phase not applicable5 trials | ||||||
| — | NCT07800273 | Sep 2026 → May 2027 expected | chronic rhinosinusitis | Liaquat University of Medical & Health Sciences | Not yet recruiting | No outcome recorded |
| — | NCT07527260 | Apr 2026 → Apr 2027 expected | allergic rhinitis | Tongji Hospital | Not yet recruiting | No outcome recorded |
| — | NCT06780644 | Feb → May 2025 overdue | hyperpigmentation of the skin | Indonesia University | Not yet recruiting | No outcome recorded |
| — | NCT06077019 | Oct 2023 → Jul 2026 overdue | — | Morten Hostrup, PhD | Recruiting | No outcome recorded |
| — | NCT07777796 | Jul 2022 → Jul 2026 | chronic rhinitis | Silesian University of Medicine | Completed | No outcome recorded |
| Comparator or background therapy67 trials | ||||||
| Phase 0 | NCT07016763 Comparator | Sep 2024 → Mar 2025 | allergic rhinitis | Isola Tiberina - Gemelli Isola Hospital, Rome, Italy | Completed | No outcome recorded |
| Phase 0 | NCT05293119 Comparator | May 2022 → May 2023 | vitiligo | Pi Research Consultancy Center, Bangladesh | Unknown | No outcome recorded |
| Phase 0 | NCT05017454 Comparator | May 2021 → Jan 2023 | alopecia areata | Kasr El Aini Hospital | Completed | No outcome recorded |
| Phase 0 | NCT03491098 Comparator | May 2018 → Apr 2019 | otitis media with effusion | Muteea Mubark Salmen Bakuwiri | Unknown | No outcome recorded |
| Phase 1 | NCT02588326 Comparator | Sep 2018 → Jul 2020 | hypersensitivity reaction disease | University of Florida | Completed | No outcome recorded |
| Phase 1 | NCT02109185 Comparator | Sep → Oct 2013 | seasonal allergic rhinitis | Mylan Pharmaceuticals Inc | Completed | No outcome recorded |
| Phase 1/2 | NCT01523236 Comparator | Dec 2011 → Jan 2012 | seasonal allergic rhinitis | Teva Pharmaceuticals USA | Completed | No outcome recorded |
| Phase 2 | NCT07016113 Comparator | Jul → Oct 2025 overdue | vitiligo | Padjadjaran University | Not yet recruiting | No outcome recorded |
| Phase 2 | NCT06914908 Background | May 2025 → Jan 2031 expected | chronic rhinosinusitis | Sanofi | Enrolling by invitation | No outcome recorded |
| Phase 2 | NCT06691113 Background | Dec 2024 → Mar 2026 overdue | chronic rhinosinusitis | Sanofi | Active not recruiting | No outcome recorded |
| Phase 2 | NCT06013241 Background | Oct 2023 → Sep 2025 | chronic rhinosinusitis | Insmed Incorporated | Completed | Missed primary |
| Phase 2 | NCT04499235 Background | Jan 2020 → Mar 2021 | bullous pemphigoid | Alkahest, Inc. | Terminated | No outcome recorded |
| Phase 2 | NCT03614923 Background | Nov 2018 → Sep 2020 | chronic rhinosinusitis | AnaptysBio, Inc. | Completed | Missed primary |
| Phase 2 | NCT04532736 Comparator | Sep 2017 → Mar 2019 | nasal cavity polyp | Dokuz Eylul University | Completed | No outcome recorded |
| Phase 2 | NCT02874144 Background | Jun 2016 → Jan 2020 | nasal cavity polyp | Northwestern University | Completed | No outcome recorded |
| Phase 2 | NCT02573233 Background | Jan 2016 → Jan 2018 | asthma | Sanofi | Completed | Mixed |
| Phase 2 | NCT01609478 Background | Aug 2012 → Jul 2013 | asthma | Novartis Pharmaceuticals | Completed | No outcome recorded |
| Phase 2 | NCT01119313 Comparator | Feb → Mar 2010 | atopic eczema | Almirall, S.A. | Completed | No outcome recorded |
| Phase 2 | NCT00784732 Comparator | Sep → Dec 2008 | seasonal allergic rhinitis | Novartis | Completed | No outcome recorded |
| Phase 2 | NCT00552110 Comparator | Jul 2007 → Feb 2008 | seasonal allergic rhinitis | Organon and Co | Completed | No outcome recorded |
| Phase 2 | NCT01228656 Comparator | Sep 2006 → Oct 2010 | psoriasis | Azidus Brasil | Suspended | No outcome recorded |
| Phase 2 | NCT00750750 Comparator | Jan → Sep 2003 | sinusitis | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT06834347 Background | Feb 2025 → Oct 2026 expected | chronic rhinosinusitis | Sanofi | Active not recruiting | No outcome recorded |
| Phase 3 | NCT06834360 Background | Feb 2025 → Nov 2026 expected | chronic rhinosinusitis | Sanofi | Active not recruiting | No outcome recorded |
| Phase 3 | NCT07311759 Comparator | Aug 2024 → Dec 2025 overdue | paronychia | Cairo University | Active not recruiting | No outcome recorded |
| Phase 3 | NCT05545072 Background | Oct 2023 → Jul 2024 | chronic rhinosinusitis | Emory University | Terminated | No outcome recorded Stop: Business |
| Phase 3 | NCT04670653 Comparator | Aug 2022 → Jul 2023 | allergic rhinitis | EMS | Withdrawn | No outcome recorded Stop: Business |
| Phase 3 | NCT05390255 Background | May 2022 → Dec 2024 | sinusitis | Beijing Tongren Hospital | Unknown | No outcome recorded |
| Phase 3 | NCT04851964 Background | Apr 2021 → Sep 2024 | chronic rhinosinusitis | AstraZeneca | Completed | Met primary |
| Phase 3 | NCT03401229 Comparator | Jan 2018 → Jul 2020 | nasal cavity polyp | AstraZeneca | Completed | Met primary |
| Phase 3 | NCT03085797 Background | May 2017 → Dec 2019 | nasal cavity polyp | GlaxoSmithKline | Completed | Met primary |
| Phase 3 | NCT02912468 Background | Dec 2016 → Jul 2018 | chronic rhinosinusitis | Sanofi | Completed | Met primary |
| Phase 3 | NCT02898454 Background | Nov 2016 → Aug 2018 | chronic rhinosinusitis | Sanofi | Completed | Met primary |
| Phase 3 | NCT02554786 Comparator | Dec 2015 → Nov 2018 | asthma | Novartis Pharmaceuticals | Completed | Met primary |
| Phase 3 | NCT02478398 Background | Jul 2015 → Nov 2018 | seasonal allergic rhinitis | Merck Sharp & Dohme LLC | Completed | Met primary |
| Phase 3 | NCT02498509 Comparator | May 2015 → Mar 2016 | perennial allergic rhinitis | Chong Kun Dang Pharmaceutical | Completed | No outcome recorded |
| Phase 3 | NCT01700192 Background | Jan 2013 → Apr 2015 | perennial allergic rhinitis | ALK-Abelló A/S | Completed | Met primary |
| Phase 3 | NCT01026870 Comparator | Jun 2012 → Dec 2013 | asthma | Organon and Co | Withdrawn | No outcome recorded |
| Phase 3 | NCT01372865 Comparator | Jun 2012 → Feb 2013 | allergic rhinitis | Eurofarma Laboratorios S.A. | Completed | No outcome recorded |
| Phase 3 | NCT01671852 Comparator | May 2012 → Jul 2015 | obstructive sleep apnea syndrome | Children's & Women's Health Centre of British Columbia | Withdrawn | No outcome recorded Stop: Business |
| Phase 3 | NCT01470053 Comparator | Mar → Dec 2011 | perennial allergic rhinitis | Hanlim Pharm. Co., Ltd. | Completed | No outcome recorded |
| Phase 3 | NCT00604500 Background | Mar → Nov 2008 | asthma, chronic obstructive pulmonary disease | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00550550 Background | Nov 2007 → Sep 2009 | allergic rhinitis, conjunctivitis | ALK-Abelló A/S | Completed | Met primary |
| Phase 3 | NCT00779740 Comparator | Feb → Apr 2005 | perennial allergic rhinitis | Organon and Co | Completed | No outcome recorded |
| Phase 3 | NCT00751075 Comparator | Dec 2003 → May 2004 | sinusitis | Organon and Co | Completed | No outcome recorded |
| Phase 4 | NCT07532993 Comparator | Sep 2026 → Feb 2027 expected | allergic rhinitis | Liaquat National Hospital & Medical College | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT06801353 Background | Feb → Dec 2025 overdue | chronic rhinosinusitis | Beijing Tongren Hospital | Not yet recruiting | No outcome recorded |
| Phase 4 | NCT05578482 Comparator | Oct 2022 → May 2023 | atopic eczema | Jacob Pontoppidan Thyssen | Unknown | No outcome recorded |
| Phase 4 | NCT04596189 Background | May 2021 → Apr 2024 | chronic rhinosinusitis | University of Montreal Hospital Centre (CHUM) | Completed | No outcome recorded |
| Phase 4 | NCT04271007 Comparator | Nov 2020 → Jul 2023 | atopic eczema | Libbs Farmacêutica LTDA | Completed | No outcome recorded |
| Phase 4 | NCT05040828 Background | Jul → Sep 2020 | seasonal allergic rhinitis | Beijing Tongren Hospital | Completed | No outcome recorded |
| Phase 4 | NCT02557269 Background | May → Oct 2015 | seasonal allergic rhinitis | Association Asthma, Bulgaria | Unknown | No outcome recorded |
| Phase 4 | NCT02559440 Comparator | Feb 2014 → Feb 2015 | adenoid hypertrophy | Guangzhou Women and Children's Medical Center | Completed | No outcome recorded |
| Phase 4 | NCT01082393 Comparator | Feb 2010 → Sep 2015 | vitiligo | University Hospital, Ghent | Completed | No outcome recorded |
| Phase 4 | NCT01333410 Comparator | Jun 2009 → Jun 2013 | vitiligo | Mahidol University | Unknown | No outcome recorded |
| Phase 4 | NCT01108198 Comparator | Oct 2006 → Jun 2011 | phimosis | University of Oulu | Unknown | No outcome recorded |
| Phase 4 | NCT00817050 Comparator | Dec 2004 → Jan 2005 | allergic rhinitis | Organon and Co | Completed | No outcome recorded |
| — | NCT07525505 Comparator | Jan → Jun 2026 overdue | atopic eczema, otitis externa | Bezmialem Vakif University | Recruiting | No outcome recorded |
| — | NCT07114107 Background | Aug 2025 → Mar 2026 overdue | allergic asthma, allergic rhinitis | Second Affiliated Hospital, School of Medicine, Zhejiang University | Not yet recruiting | No outcome recorded |
| — | NCT05919316 Comparator | Jul 2023 → Oct 2024 | allergic rhinitis | National University of Malaysia | Completed | No outcome recorded |
| — | NCT05912192 Comparator | Feb 2022 → Apr 2023 | allergic rhinitis | National University of Malaysia | Completed | No outcome recorded |
| — | NCT05228483 Comparator | Nov 2021 → Nov 2023 | vulvar lichen sclerosus | Xijing Hospital | Unknown | No outcome recorded |
| — | NCT05348148 Comparator | Jun 2020 → Mar 2032 expected | vasomotor rhinitis | Camillians Saint Mary's Hospital Luodong | Recruiting | No outcome recorded |
| — | NCT04085744 Comparator | Nov 2019 → Jun 2020 | pharyngitis | Derince Training and Research Hospital | Completed | No outcome recorded |
| — | NCT03451318 Comparator | Mar 2018 → May 2019 | obstructive sleep apnea syndrome | Shanghai Stomotological Hospital | Unknown | No outcome recorded |
| — | NCT00967967 Background | Mar 2009 → Jun 2014 | allergic rhinitis, asthma | Laval University | Suspended | No outcome recorded |
| — | NCT00618332 Comparator | Apr → Jul 2008 | seasonal allergic rhinitis | University of Chicago | Completed | No outcome recorded |
News releases announcing trial results or a regulatory action · 42
| Date | Issuer | Release |
|---|---|---|
| 2026-07-21 | Glenmark Pharmaceuticals Ltd. India | Regulatory Glenmark Receives U.S. FDA Approval to Expand the Use of RYALTRIS® Nasal Spray for Children Aged 6 to Less Than 12 Years glenmarkpharma.com ↗
With this approval, RYALTRIS® is now approved in the United States for adults and pediatric patients aged 6 years and older, extending this treatment option to a younger pediatric population. |
| 2025-11-10 | Glenmark Pharmaceuticals Ltd. India | Regulatory Glenmark Secures China Approval For RYALTRIS®, Reinforcing Respiratory Innovation Leadership glenmarkpharma.com ↗
Glenmark Specialty S.A., a wholly-owned subsidiary of Glenmark Pharmaceuticals Ltd., today announced that the National Medical Products Administration (NMPA) of China has approved RYALTRIS® Compound Nasal Spray (GSP 301 NS) for the treatment of Allergic Rhinitis (AR) in adults and children – specifically for treatment of moderate to severe seasonal AR in adults and pediatric patients 6 years of age and older, and moderate to severe perennial AR in adult s and pediatric patients 12 years of age and older. |
| 2025-06-02 | Lyra Therapeutics | Results Lyra Therapeutics Reports Positive Results from the ENLIGHTEN 2 Phase 3 Trial of LYR-210 Achieving Statistically Significant Results for Primary and Key Secondary Endpoints in the Treatment of Chronic Rhinosinusitis (CRS) lyratherapeutics.com ↗
ENLIGHTEN 2 trial met primary endpoint with LYR-210 demonstrating statistically significant improvement in the composite of the three cardinal symptoms (3CS) of CRS at 24 weeks (p=0.0078) |
| 2025-05-07 | Lyra Therapeutics | Results Lyra Therapeutics to Present 52-week Extension Stage Results for ENLIGHTEN 1 Phase 3 Study for LYR-210 for the Treatment of Chronic Rhinosinusitis at COSM 2025 lyratherapeutics.com ↗
Repeat LYR-210 treatment demonstrated a favorable safety profile, similar to that observed in the Primary Study Stage in patients with CRS. |
| 2024-11-12 | Lyra Therapeutics | Results Lyra Therapeutics Reports Third Quarter 2024 Financial Results and Provides Corporate Update lyratherapeutics.com ↗
Safety data for LYR-210 was generally consistent with the 24-week primary treatment phase, including for those patients that received a repeat dosing, resulting in a 12-month treatment period. |
| 2024-08-14 | Lyra Therapeutics | Results Lyra Therapeutics Reports Second Quarter 2024 Financial Results and Provides Corporate Update lyratherapeutics.com ↗
In parallel, the company continues to analyze data from ENLIGHTEN 1; further analysis of the ENLIGHTEN 1 data has revealed that LYR-210 demonstrated improvement over control in symptomatic endpoints in the CRS patient cohort with nasal polyps |
| 2024-05-06 | Lyra Therapeutics | Results Lyra Therapeutics Reports Topline Results from Phase 3 ENLIGHTEN 1 Trial for LYR-210 in Chronic Rhinosinusitis lyratherapeutics.com ↗
ENLIGHTEN 1 did not meet its primary endpoint of demonstrating statistically significant improvement compared to sham control in the composite score of the three cardinal symptoms (3CS) of CRS (nasal obstruction, nasal discharge, facial pain/pressure) at 24 weeks. |
| 2023-11-07 | Lyra Therapeutics | Results Lyra Therapeutics Reports Third Quarter 2023 Financial Results and Provides Corporate Update lyratherapeutics.com ↗
Data evaluating computed tomography (CT) scans, a pre-specified secondary endpoint, demonstrated statistically significant improvement in ethmoid sinus opacification in patients who received LYR-220, compared to sham control at week 24 (p=0.035). |
| 2023-09-12 | Lyra Therapeutics | Results Lyra Therapeutics Announces Positive Topline Results from BEACON Phase 2 Study of LYR-220 for the Treatment of Chronic Rhinosinusitis (CRS) in Patients with Prior Ethmoid Sinus Surgery lyratherapeutics.com ↗
Lyra Therapeutics, Inc. (Nasdaq: LYRA) (“Lyra” or the “Company”), a clinical-stage biotechnology company developing innovative therapies for the localized treatment of chronic rhinosinusitis (CRS), today announced positive topline results from the BEACON Phase 2 clinical study of LYR-220 in adult patients with CRS, with and without polyps, who have had prior ethmoid sinus surgery. |
| 2023-07-03 | Impax Laboratories, LLC | Regulatory Amneal Launches Authorized Generic for Xyrem® (sodium oxybate) and Receives FDA Approval for Five Complex Generics in the Second Quarter amneal.com ↗
In addition, the Company announced it has received Abbreviated New Drug Application (ANDA) approvals from the U.S. Food and Drug Administration (“FDA”) for five complex generics products. |
| 2022-09-23 | Glenmark Pharmaceuticals Ltd. India | Regulatory Bausch Health and Glenmark Announce the approval of RYALTRIS® in Canada glenmarkpharma.com ↗
RYALTRIS ® (olopatadine hydrochloride and mometasone furoate nasal sp ray) has been approved by Health Canada for the symptomatic treatment of moderate to severe seasonal allergic rhinitis (SAR) and associated ocular symptoms in adults, adolescents, and children aged 6 years and older. |
| 2022-09-10 | Lyra Therapeutics | Results Lyra Therapeutics Announces Additional Data Presentations from Phase 2 LANTERN Study at the American Rhinologic Society Annual Meeting lyratherapeutics.com ↗
Compared to control, significantly higher proportions of LYR-210-treated subjects improved from moderate or severe at baseline to mild or none at week 24 in nasal blockage, nasal discharge, and facial pain/pressure (p<0.05). |
| 2022-04-29 | Lyra Therapeutics | Results Lyra Therapeutics Presents Positive Data from LANTERN Phase 2 Study of LYR-210 for Treatment of Chronic Rhinosinusitis at COSM 2022 lyratherapeutics.com ↗
In the LANTERN Phase 2 study, LYR-210 (7500 µg) demonstrated rapid, clinically meaningful and durable symptom improvement in a composite score of CRS cardinal symptoms over six months. |
| 2022-03-17 | Perrigo Company | Regulatory PERRIGO ANNOUNCES U.S. FDA APPROVAL FOR OTC USE OF NASONEX® 24HR ALLERGY perrigo.com ↗
Perrigo Company plc (NYSE: PRGO), a leading provider of Quality, Affordable Self-Care Products, today announced that it has received final approval from the U.S. Food and Drug Administration for the over-the-counter use of Nasonex® 24HR Allergy (mometasone furoate monohydrate 50mcg). |
| 2021-11-09 | Lyra Therapeutics | Results Lyra Therapeutics Reports Third Quarter 2021 Financial Results and Provides Corporate Update lyratherapeutics.com ↗
The recently completed pharmacokinetic (PK) study showed that Mometasone Furoate (MF) blood levels were constant over the 56 days, providing further evidence that LYR-210 delivers a steady daily dose of MF with accompanying rapid symptom relief during this time period. |
| 2021-10-04 | Lyra Therapeutics | Results Lyra Therapeutics Presents New Positive Phase 2 LANTERN 6-Month Follow-Up and LYR-210 Pharmacokinetic Data, and LANTERN Manuscript Wins Award at the 67th Annual Meeting of the American Rhinologic Society lyratherapeutics.com ↗
LYR-210 pharmacokinetics indicate a constant and steady daily dose of Mometasone Furoate is delivered to patients |
| 2021-09-30 | Glenmark Pharmaceuticals Ltd. India | Regulatory Glenmark receives marketing approval for Ryaltris®, an innovative combination nasal spray, in 13 countries across the EU and UK glenmarkpharma.com ↗ |
| 2021-09-21 | Lyra Therapeutics | Results Lyra Therapeutics Announces Publication of Positive LANTERN Results in the International Forum of Allergy & Rhinology lyratherapeutics.com ↗
LYR-210 (7500 µg) was shown to be safe and well-tolerated over the 24-week treatment period and demonstrated statistically significant, rapid, durable, dose-dependent global symptom improvement based on composite Cardinal Symptoms (CS) scores and Sino-Nasal Outcome Test (SNOT-22). |
| 2021-09-09 | Lyra Therapeutics | Results Lyra Therapeutics Announces Publication of Preclinical Pharmacokinetics and Drug Release characterization for XTreo™ Technology Platform in the American Journal of Rhinology & Allergy lyratherapeutics.com ↗
The results demonstrate that XTreo™ MF provides targeted, sustained and efficient dosing to local sinus tissues that is superior to intranasal corticosteroid sprays (INCS). |
| 2021-09-03 | Novartis Pharmaceuticals | Results Novartis presents new findings at ERS reinforcing the efficacy of Enerzair® Breezhaler®, highlighting its digital companion, as well as showcasing commitment to low carbon footprint asthma solutions novartis.com ↗ |
| 2021-06-30 | Lyra Therapeutics | Results Lyra Therapeutics Announces Positive Topline Results of Pharmacokinetic Study of LYR-210 in Patients with Chronic Rhinosinusitis lyratherapeutics.com ↗
Data obtained from the study are supportive of LYR-210’s safety profile and provide a PK bridge to the established safety of mometasone furoate (MF) for a 505(b)(2) pathway for New Drug Approval (NDA) submission. |
| 2021-04-26 | Glenmark Pharmaceuticals Ltd. India | Regulatory Glenmark’s Ryaltris ® nasal spray now approved in Europe for the first line treatment of allergic rhinitis in patients over 12 years of age glenmarkpharma.com ↗
Glenmark’s Ryaltris ® nasal spray now approved in Europe for the first line treatment of allergic rhinitis in patients over 12 years of age |
| 2021-04-11 | Lyra Therapeutics | Results Lyra Therapeutics Presents Positive Full Data Set from LANTERN Phase 2 Study of LYR-210 at COSM 2021 Virtual lyratherapeutics.com ↗
Separately, Lyra also reported an analysis showing that LYR-210 (7500µg) achieved statistically significant improvement across 3 cardinal symptoms at week 24 in the LANTERN study |
| 2021-02-22 | Glenmark Pharmaceuticals Ltd. India | Regulatory Glenmark’s Ryaltris®- innovative single nasal spray, ready to market in Russia glenmarkpharma.com ↗
Marketing approval received from the Ministry of Health of the Russian Federation |
| 2020-12-07 | Lyra Therapeutics | Results Lyra Therapeutics Announces Positive Topline Results for LANTERN Phase 2 Randomized Controlled Study of LYR-210 for the Treatment of Chronic Rhinosinusitis With and Without Nasal Polyps lyratherapeutics.com ↗
7500 mcg dose of LYR-210 achieved statistically significant improvement in a composite of the 4 cardinal symptoms of CRS at weeks 16 (p=0.021), 20 (p=0.012) and 24 (p=0.016) compared to control. |
| 2020-09-10 | Lyra Therapeutics | Results Lyra Therapeutics Presents Clinical Data Demonstrating LYR-210’s Local Anti Inflammatory Effects for the Treatment of Chronic Rhinosinusitis lyratherapeutics.com ↗
today announced the presentation of data showing that LYR-210 demonstrated a significant reduction of sinonasal Type 2 inflammation in surgically naïve patients with chronic rhinosinusitis (CRS). |
| 2020-09-07 | Novartis Pharmaceuticals | Results Novartis post hoc analysis shows high-dose Enerzair® Breezhaler® reduces asthma exacerbations versus medium-dose, complementing key pivotal IRIDIUM study findings novartis.com ↗
High-dose, once-daily Enerzair ® Breezhaler ® [IND/GLY/MF] reduced asthma exacerbation rates by 21% (moderate or severe) and 31% (severe) versus medium-dose, over 52 weeks |
| 2020-07-07 | Novartis Pharmaceuticals | Regulatory Novartis receives EC approval for Enerzair® Breezhaler®, including the first digital companion (sensor and app) that can be prescribed alongside a treatment for uncontrolled asthma in the EU novartis.com ↗
European Commission approves once-daily Enerzair ® Breezhaler ® (QVM149; IND/GLY/MF) in the EU, the first-in-class LABA/LAMA/ICS fixed-dose combination for patients whose asthma is uncontrolled with LABA/ICS |
| 2020-06-29 | Novartis Pharmaceuticals | Regulatory Novartis receives simultaneous approval for five new products from Japanese Ministry of Health, Labour and Welfare, offering Japanese patients a broad range of novel treatment options novartis.com ↗ |
| 2020-06-05 | Novartis Pharmaceuticals | Results Novartis Phase IIIb ARGON study meets primary endpoint in a comparison of Enerzair® Breezhaler® (QVM149) versus a free combination of two existing inhaled treatments in uncontrolled asthma novartis.com ↗
Once-daily Enerzair ® Breezhaler ® (QVM149; IND/GLY/MF) met primary endpoint, demonstrating non-inferiority to a free combination of twice-daily Sal/Flu plus once-daily tiotropium (Tio), in improving quality of life in people with uncontrolled asthma 1 . |
| 2020-05-01 | Novartis Pharmaceuticals | Regulatory Novartis receives CHMP positive opinion for Enerzair® Breezhaler® (QVM149), a potential first-in-class inhaled LABA/LAMA/ICS combination for uncontrolled asthma novartis.com ↗ |
| 2020-01-06 | Lyra Therapeutics | Regulatory Lyra Therapeutics Announces FDA Clearance of Investigational New Drug Application for a Phase 2 Clinical Trial of LYR-210 for Chronic Rhinosinusitis lyratherapeutics.com ↗
today announced that the U.S. Food and Drug Administration (FDA) has cleared the company’s Investigational New Drug (IND) application for LYR-210 for the treatment of chronic rhinosinusitis (CRS), a debilitating chronic disease affecting millions of patients. |
| 2019-12-20 | Glenmark Pharmaceuticals Ltd. India | Regulatory Glenmark Pharmaceuticals announces product approval for Ryaltris(R) in Australia glenmarkpharma.com ↗ |
| 2019-12-06 | Novartis Pharmaceuticals | Results Novartis Phase III data on new inhaled dual combination QMF149 show significant improvement across key asthma outcomes versus monotherapy novartis.com ↗
Once-daily QMF149 met primary endpoint of lung function improvement and key secondary endpoint of asthma control improvement versus mometasone furoate |
| 2019-09-30 | Novartis Pharmaceuticals | Results Novartis announces positive results from Phase III PALLADIUM study of inhaled combination QMF149 in patients with uncontrolled asthma novartis.com ↗
Novartis today announced that investigational, once-daily, fixed-dose inhaled QMF149 (indacaterol acetate and mometasone furoate or IND/MF) was superior to mometasone furoate (MF) in improving trough forced expiratory volume in one second (FEV 1 ) after 26 weeks |
| 2019-09-30 | Novartis Pharmaceuticals | Results Novartis announces positive results from Phase III IRIDIUM study of inhaled combination QVM149 in patients with uncontrolled asthma novartis.com ↗
Once-daily QVM149 demonstrated statistically significant improvement in lung function versus QMF149, meeting primary endpoint[1],[2] |
| 2019-05-09 | Glenmark Pharmaceuticals Ltd. India | Results Glenmark Pharmaceuticals Announces Results from a Phase 3 Study of Ryaltris™, an Investigational Product for the Treatment of Seasonal Allergic Rhinitis, in Patients Aged 6 to Under 12 Years glenmarkpharma.com ↗ |
| 2019-04-25 | Glenmark Pharmaceuticals Ltd. India | Regulatory Glenmark receives approval from Russian Ministry of Healthcare to market Momate Rhino metered nasal spray as an Over-the-Counter (OTC) product glenmarkpharma.com ↗ |
| 2018-08-08 | Glenmark Pharmaceuticals Ltd. India | Regulatory Glenmark Pharmaceuticals Announces FDA Acceptance of the Company’s First New Drug Application for Ryaltris™ for Patients with Seasonal Allergic Rhinitis glenmarkpharma.com ↗
Glenmark Pharmaceuticals Announces FDA Acceptance of the Company’s First New Drug Application for Ryaltris™ for Patients with Seasonal Allergic Rhinitis |
| 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, |
| 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. |
| 2005-04-11 | Perrigo Company | Regulatory Perrigo Company Announces FDA Approval For Mometasone Furoate Topical Solution perrigo.com ↗
The Perrigo Company (NASDAQ: PRGO)(TASE: PRGO) today announced that its Agis Industries subsidiary has received approval from the U.S. Food and Drug Administration (FDA) to manufacture and market Mometasone Furoate Topical Solution USP, 0.1% (Lotion). |
All press releases naming this drug 62 releases
Evidence & citations 17 cited values
Every value below carries the sentence it was read from. 179 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | mometasone furoate | “Apply triple combination cream containing mometasone furoate 0.1%, hydroquinone 4%, tretinoin 0.05% at night all over the face except the area around the eyes, 1 fingertip unit...” NCT06780644 ↗165“Participants received modified Kligman's formula consisting of hydroquinone 4%, tretinoin 0.05%, and mometasone furoate 0.1% immediately after standardized microneedling with a...” NCT07696806 ↗ “Efficacy and Safety of 200mcg BID Mometasone Furoate Nasal Spray (MFNS) Versus Placebo as Adjunctive Treatment to Antibiotics in Relief of Symptoms of Acute Bacterial Sinusitis” NCT00423176 ↗ “Schools were purposively selected, matched, and randomized to receive 9 months of supervised therapy with mometasone furoate or usual care.” PMID 30118728 ↗ Aug 2018 “QVM149: Indacaterol as acetate 150 µg / glycopyrronium as bromide 50 µg / mometasone furoate 160 µg once daily delivered via Breezhaler®” NCT05776927 ↗ “LYR-210 is a drug depot, which contains the anti-inflammatory medication mometasone furoate (MF) pre-loaded in a single use applicator.” NCT04041609 ↗ “GSP301 nasal spray is a fixed-dose combination of olopatadine hydrochloride (antihistamine) and mometasone furoate (corticosteroid).” PMID 30910440 ↗ Mar 2019 “The device loaded with mometasone furoate (ESO-101) is under investigation for the treatment of eosinophilic oesophagitis (EoE).” PMID 39676687 ↗ Dec 2024 “QVM149 150/50/160 μg (indacaterol acetate/glycopyrronium/mometasone furoate) once daily (o.d.) delivered via Concept1 device” NCT02571777 ↗ “mometasone furoate spray will be applied on the cuff of the intubation tube topically and patient will be intubated.” NCT04085744 ↗ “In-office bilateral placement of the S8 Sinus Implant (mometasone furoate, 1350 mcg) in the ethmoid sinuses” NCT03358329 ↗ |
| Known as | Elocon | “Elocon® mometasone furoate 0.1% cream” NCT02973776 ↗ |
| Known as | LYR-210 | “LYR-210 drug matrix (mometasone furoate)” NCT05295459 ↗ |
| Known as | LYR-220 | “LYR-220 drug matrix (mometasone furoate 7500 µg) Design 1” NCT05035654 ↗ |
| Known as | MFNS | “This is a Phase 4 randomized, placebo-controlled, parallel-group, single-center, double-blind study to evaluate the effects of mometasone furoate nasal spray (MFNS) in subjects...” NCT00359216 ↗24“A Double-Blind Placebo-Controlled, Randomized, Parallel-Group, Single-Site Study Of Mometasone Furoate Nasal Spray (MFNS) In Subjects With Mild-Moderate Obstructive Sleep...” NCT00491374 ↗ “The purpose of this study is to determine whether 8 weeks treatment with mometasone furoate nasal spray (MFNS), twice daily, is safe and effective in treating adenoid...” NCT00552032 ↗ “Efficacy and Safety of 200mcg BID Mometasone Furoate Nasal Spray (MFNS) Versus Placebo as Adjunctive Treatment to Antibiotics in Relief of Symptoms of Acute Bacterial Sinusitis” NCT00423176 ↗ “Mometasone furoate nasal spray (MFNS), a potent intranasal corticosteroid with proved efficacy in relieving nasal allergic rhinitis symptoms” PMID 20434199 ↗ Jun 2010 “Mometasone Furoate Nasal Spray (MFNS) - intranasal corticosteroid - 2 doses (1 dose = 50 micrograms/actuation) in each nostril twice daily.” NCT03401229 ↗ “Mometasone furoate nasal spray (MFNS) 200 mcg QD in the Relief of Nasal Congestion Associated With Seasonal Allergic Rhinitis (SAR)” NCT00732381 ↗ “The intranasal corticosteroid mometasone furoate nasal spray (MFNS) is effective for AR symptoms including nasal congestion” PMID 23562197 ↗ Mar 2013 “mometasone furoate nasal spray (MFNS) versus amoxicillin and placebo in patients with acute, uncomplicated rhinosinusitis.” PMID 16337461 ↗ Oct 2005 “Mometasone furoate nasal spray (MFNS) 200 mcg once daily (two 50 mcg puffs per nostril) in the morning.” NCT00599027 ↗ “Mometasone furoate nasal spray (MFNS) has established efficacy in treating nasal allergy symptoms” PMID 21439168 ↗ Mar 2011 |
| Known as | MMF | “PURPOSE: A two-arm, double-blind, randomized trial was performed to evaluate the effect of 0.1% mometasone furoate (MMF) on acute skin-related toxicity in patients undergoing...” PMID 20800381 ↗ Aug 20101“Mometasone furoate (MMF) 0.1% ointment” NCT05228483 ↗ |
| Known as | mometasone | “In this double-blind study, eligible patients (≥12 years of age) with SAR were randomized 1:1:1:1 to twice-daily GSP301 (665 μg of olopatadine and 25 μg of mometasone),...” PMID 30910440 ↗ Mar 20192“Mometasone is an inhaled corticosteroid (ICS), which reduces the inflammation in the airways.” NCT01471340 ↗ “Nasonex® (mometasone) versus Flonase® nasal spray” NCT00817050 ↗ |
| Known as | Mometasone Furoate Cream | “Generic name :Mometasone Furoate Cream. Dosage form:Each gram of Mometasone Furoate Cream contains mometasone furoate, USP in a cream base of hexylene glycol, phosphoric acid,...” NCT02495064 ↗ |
| Known as | mometasone furoate monohydrate | “Mometasone furoate monohydrate nasal spray 50 mcg was dosed intranasally at a dose of one spray in each nostril once daily for participants aged 5 to \<12 years” NCT00550550 ↗5“Treatment C: Ryaltris (Active Control) - mometasone furoate monohydrate and olopatadine hydrochloride nasal spray” NCT06126952 ↗ “Mometasone furoate monohydrate nasal spray 50 mcg administered intranasally as needed for rescue medication.” NCT01700192 ↗ “Nasonex (mometasone furoate monohydrate) Nasal Spray, 50 mcg.” NCT02125253 ↗ |
| Known as | Mometasone Furoate Nasal Spray | “Mometasone Furoate Nasal Spray (MFNS) - intranasal corticosteroid - 2 doses (1 dose = 50 micrograms/actuation) in each nostril twice daily.” NCT03401229 ↗1“Mometasone furoate nasal spray (MFNS) 200 mcg QD in the Relief of Nasal Congestion Associated With Seasonal Allergic Rhinitis (SAR)” NCT00732381 ↗ |
| Known as | Nasonex | “This study will hope to show that the treatment of the patient's perennial allergic rhinitis (PAR) using Nasonex® (mometasone furoate nasal spray) will result in improvement of...” NCT00491374 ↗10“The purpose of this study is to evaluate the efficacy and safety of Nasonex® (mometasone furoate nasal spray), when used together with an antibiotic, for the relief of symptoms...” NCT00423176 ↗ “The purpose of this study is to determine if one allergy treatment (0.15% azelastine hydrochloride) is as safe as mometasone furoate (nasonex) alone.” NCT00720382 ↗ “Nasonex (mometasone furoate monohydrate) Nasal Spray, 50 mcg.” NCT02125253 ↗ “Mometasone Furoate Aqueous Nasal Spray [Nasonex®] 200mcg QD” NCT00224523 ↗ “Mometasone furoate (Nasonex®) 50 mcg/actuation nasal spray” NCT01038427 ↗ “Mometasone Furoate Nasal Spray NASONEX” NCT03451318 ↗ “Nasal Steroid (Nasonex, Flonase)” NCT02874144 ↗ |
| Known as | Nasonex Nasal Spray | “Mometasone furoate will be available in the form of Nasonex Nasal Spray.” NCT05919316 ↗ |
| Known as | SCH 32088 | “Dose-Ranging Study of Mometasone Furoate Nasal Spray (SCH 32088) in the Treatment of Children (Ages 6-11) With Seasonal Allergic Rhinitis (Protocol C95-161)” NCT03879772 ↗1“SCH 32088 mometasone furoate (MF) metered-dose inhaler” NCT01026870 ↗ |
| Known as | SINUVA (mometasone furoate) sinus implant | “SINUVA (mometasone furoate) sinus implant” NCT01732536 ↗1“SINUVA (mometasone furoate) sinus implant” NCT02291549 ↗ |
| Known as | Topison | “Comparative Study:Topison (Mometasone Furoate) Versus Two Others Mometasone Furoates” NCT04271007 ↗ |
| Modality | Other / unclassified | “RATIONALE: Steroid therapy, such as mometasone furoate, may prevent radiation dermatitis caused by radiation therapy.” NCT00438659 ↗ |
| Route | Intranasal | “Mometasone Furoate Aqueous Nasal Spray [Nasonex®] 200mcg QD” NCT00224523 ↗ |