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  1. pharmadog
  2. ›drugs
  3. ›Fluticasone Propionate
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Fluticasone Propionate Glenmark

Marketedupdated 3mo ago
by Glenmark Pharmaceuticals Ltd
Approved
community read0 votes

🐶 often sniffed alongside

top 7
  • tagApproval30 co-mentions · 14 sources
  • drugFLUTICASONE PROPIONATE26 co-mentions · 14 sources
  • drugFlovent17 co-mentions · 14 sources
  • drugFlovent HFA17 co-mentions · 14 sources
  • drugCutivate17 co-mentions · 14 sources
  • drugsalmeterol xinafoate2 co-mentions · 1 sources
  • companyAurobindo Pharma Ltd2 co-mentions · 2 sources

Small molecule drug with a maximum clinical stage of Approval (across all indications), with 11 approved and 14 investigational indications.

indications

investigational
Psoriasis

all catalysts(3)

approval · 3
May 10, 2024
approval
2y ago
FLUTICASONE PROPIONATE — FDA approval
Fluticasone Propionate Glenmark
→
Dec 16, 2025
approval
8mo ago
FLUTICASONE PROPIONATE — FDA approval
Fluticasone Propionate Glenmark
→
Mar 16, 2026
approval
5mo ago
FLUTICASONE PROPIONATE — FDA approval
Fluticasone Propionate Glenmark
→

Trials studying Fluticasone Propionate Glenmark

  • phase3A Study to Evaluate the Efficacy and Safety of QVM149 (Indacaterol Acetate / Glycopyrronium Bromide / Mometasone Furoate) Versus Salmeterol Xinafoate/Fluticasone Propionate in Children From 12 Years to Less Than 18 Years of Age With Asthma.recruitingn=188
  • phase4Dymista in Chinese Adolescentsnot yet recruitingn=100
  • phase4A Bronchoscopy Study to Assess the Effects of Inhaled Corticosteroids on Adult Healthy Volunteersactive not recruitingn=30
  • phase2Study on the Safety and Efficacy of PA9159 Inhalation Aerosol for the Treatment of Adult Bronchial Asthmarecruitingn=30
  • phase2Study on BI 54903 (Inhaled Corticosteroid) Administered Twice Daily Via Respimat Inhaler in Patients With Asthma Inadequately Controlled on Medium Dose Inhaled Corticosteroid (ICS).terminatedn=9
  • phase3A Study to Evaluate MK0476 and Fluticasone to Control Asthma in Patients With Mild Persistent Asthma (0476-910)completedn=994
  • phase4Effects of Mometasone Furoate Dry Powder Inhaler, Fluticasone Propionate, and Montelukast on Bone Mineral Density in Asthmatics (Study P03418)completedn=566
  • phase3Study of Inhaled Glucocorticosteroids/Long-Acting Bronchodilator Drugs in Subjects With Asthma That Have Been Taking Inhaled Glucocorticosteroids (Study P04705AM1)completedn=722
more trials →

Patent cliff

source: FDA Orange Book
first barrier falls
Aug 26, 2026
6 days

Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.

patents (118)

  • Jan 6, 2041patentUS 11173259*PED
  • Jan 6, 2041patentUS 11173259*PED
  • Jan 6, 2041patentUS 11173259*PED
  • Jan 6, 2041patentUS 11173259*PED
  • Jan 6, 2041patentUS 11173259*PED
  • Jan 6, 2041patentUS 11173259*PED
  • Jan 6, 2041patentUS 11173259*PED
  • Jul 6, 2040formulationUS 11173259
  • Jul 6, 2040formulationUS 11173259
  • Jul 6, 2040formulationUS 11173259
  • Jul 6, 2040formulationUS 11173259
  • Jul 6, 2040formulationUS 11173259
  • Jul 6, 2040formulationUS 11173259
  • Jul 6, 2040formulationUS 11173259
  • Mar 26, 2040patentUS 11344685*PED
  • Mar 26, 2040patentUS 11344685*PED
  • Mar 26, 2040patentUS 11344685*PED
  • Mar 26, 2040patentUS 11344685*PED
  • Mar 26, 2040patentUS 11344685*PED
  • Mar 26, 2040patentUS 11344685*PED
  • Mar 26, 2040patentUS 11344685*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Feb 20, 2040patentUS 11969544*PED
  • Sep 26, 2039formulationUS 11344685
  • Sep 26, 2039formulationUS 11344685
  • Sep 26, 2039formulationUS 11344685
  • Sep 26, 2039formulationUS 11344685
  • Sep 26, 2039formulationUS 11344685
  • Sep 26, 2039formulationUS 11344685
  • Sep 26, 2039formulationUS 11344685
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Aug 20, 2039formulationUS 11969544
  • Jun 14, 2036patentUS 10918816*PED
  • Jun 14, 2036patentUS 10918816*PED
  • Jun 14, 2036patentUS 10918816*PED
  • Jun 14, 2036patentUS 10918816*PED
  • Jun 14, 2036patentUS 10918816*PED
  • Jun 14, 2036patentUS 10918816*PED
  • Jun 14, 2036patentUS 10918816*PED
  • Feb 23, 2036method-of-use (U-2133)US 11554229
  • Dec 14, 2035formulationUS 10918816
  • Dec 14, 2035formulationUS 10918816
  • Dec 14, 2035formulationUS 10918816
  • Dec 14, 2035formulationUS 10918816
  • Dec 14, 2035formulationUS 10918816
  • Dec 14, 2035formulationUS 10918816
  • Dec 14, 2035formulationUS 10918816
  • Apr 6, 2035patentUS 9066957*PED
  • Apr 6, 2035patentUS 9066957*PED
  • Apr 6, 2035patentUS 9066957*PED
  • Apr 6, 2035patentUS 9066957*PED
  • Apr 6, 2035patentUS 9066957*PED
  • Apr 6, 2035patentUS 9066957*PED
  • Apr 6, 2035patentUS 9415008*PED
  • Apr 6, 2035patentUS 9415008*PED
  • Oct 6, 2034formulationUS 9066957
  • Oct 6, 2034formulationUS 9066957
  • Oct 6, 2034formulationUS 9066957
  • Oct 6, 2034formulationUS 9066957
  • Oct 6, 2034formulationUS 9066957
  • Oct 6, 2034formulationUS 9066957
  • Oct 6, 2034formulationUS 9415008
  • Oct 6, 2034formulationUS 9415008
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Aug 14, 2031patentUS 10195375*PED5.0y
  • Apr 4, 2031method-of-use (U-2133)US 120832704.6y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Feb 14, 2031formulationUS 101953754.5y
  • Aug 26, 2026patentUS 7500444*PED6d
  • Aug 26, 2026patentUS 7500444*PED6d

FDA exclusivities (2)

  • Mar 15, 2027I-940Indication (3y)207d
  • Sep 20, 2026CGTCGT31d

News(0)

no news has mentioned this drug yet

brand
Fluticasone Propionate
generic
fluticasone propionate
MOA
Glucocorticoid receptor agonist
indication
Non Allergic Rhinitis
phase
marketed
Data sources
openFDA · ClinicalTrials.gov
last refreshed 1h ago
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