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  3. ›DAPAGLIFLOZIN
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DAPAGLIFLOZIN

Marketedupdated 3mo ago
by Lupin Ltd
Approved
community read0 votes

🐶 often sniffed alongside

top 8
  • tagApproval78 co-mentions · 27 sources
  • drugDAPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE65 co-mentions · 29 sources
  • drugDAPAGLIFLOZIN AND SAXAGLIPTIN HYDROCHLORIDE65 co-mentions · 29 sources
  • tagSmall Molecule37 co-mentions · 26 sources
  • drugmetformin22 co-mentions · 10 sources
  • drugSITAGLIPTIN AND METFORMIN HYDROCHLORIDE22 co-mentions · 10 sources
  • drugmetformin hydrochloride22 co-mentions · 10 sources
  • drugmetformin hydrochloride ER22 co-mentions · 10 sources

indications

investigational
Type 2 Diabetes

all catalysts(21)

approval · 20
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE (DAPAGLIFLOZIN) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE (DAPAGLIFLOZIN, METFORMIN HYDROCHLORIDE) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE (DAPAGLIFLOZIN) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND SAXAGLIPTIN HYDROCHLORIDE (DAPAGLIFLOZIN) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND SAXAGLIPTIN HYDROCHLORIDE (DAPAGLIFLOZIN) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE (DAPAGLIFLOZIN) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE (DAPAGLIFLOZIN) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE (DAPAGLIFLOZIN) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE (DAPAGLIFLOZIN) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE (DAPAGLIFLOZIN) — FDA approval
DAPAGLIFLOZIN
→
Apr 6, 2026
approval
4mo ago
DAPAGLIFLOZIN — FDA approval
DAPAGLIFLOZIN
→
phase 1 initiation · 1
Apr 30, 2026
phase 1 initiation
4mo ago
Bio-Innova Co Ltd — dapagliflozin (Phase I Trial Initiation)
DAPAGLIFLOZIN
→
view all 21 catalysts →

Trials studying DAPAGLIFLOZIN

  • phase3A Phase III Study to Investigate the Efficacy and Safety of Elecoglipron Alone or in Combination With Dapagliflozin Compared With Placebo in Adults With Type 2 Diabetes Mellitusrecruitingn=800
  • phase3A Phase III Study to Investigate the Efficacy and Safety of the Combination of Elecoglipron and Dapagliflozin in Adults With Type 2 Diabetes Mellitusrecruitingn=2,000
  • phase4Dapagliflozin and Effect on Cardiovascular Events in Acute Heart Failure -Thrombolysis in Myocardial Infarction 68 (DAPA ACT HF-TIMI 68)completedn=2,401
  • phase4The Fontan Dapagliflozin Pilot Studyenrolling by invitationn=29
  • phase2A Phase IIb Study to Evaluate the Effect of Dapagliflozin in Combination With Baxdrostat Compared With Baxdrostat on Albuminuria in Participants With Chronic Kidney Disease and High Blood Pressure.recruitingn=218
  • phase3Study to Investigate Efficacy, Safety, and Tolerability of Zibotentan/Dapagliflozin Compared to Dapagliflozin in Participants With Chronic Kidney Disease and High Proteinuria (ZENITH High Proteinuria)active not recruitingn=1,835
  • phase3A Phase III Study to Investigate the Efficacy and Safety of Baxdrostat in Combination With Dapagliflozin on CKD Progression in Participants With CKD and High Blood Pressure.active not recruitingn=2,554
  • phase3A Study of the Effect and Safety of Sparsentan in the Treatment of Patients With IgA Nephropathyactive not recruitingn=406
more trials →

Patent cliff

source: FDA Orange Book
first barrier falls
Jun 20, 2027
309 days

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

patents (64)

  • May 12, 2031patentUS 9616028*PED4.7y
  • May 12, 2031patentUS 9616028*PED4.7y
  • May 12, 2031patentUS 9616028*PED4.7y
  • May 12, 2031patentUS 9616028*PED4.7y
  • Nov 12, 2030formulationUS 96160284.2y
  • Nov 12, 2030formulationUS 96160284.2y
  • Nov 12, 2030formulationUS 96160284.2y
  • Nov 12, 2030formulationUS 96160284.2y
  • Jun 16, 2030patentUS 7919598*PED3.8y
  • Jun 16, 2030patentUS 7919598*PED3.8y
  • Jun 16, 2030patentUS 7919598*PED3.8y
  • Jun 16, 2030patentUS 7919598*PED3.8y
  • Jun 16, 2030patentUS 7919598*PED3.8y
  • Jun 16, 2030patentUS 7919598*PED3.8y
  • Dec 16, 2029compositionUS 79195983.3y
  • Dec 16, 2029compositionUS 79195983.3y
  • Dec 16, 2029compositionUS 79195983.3y
  • Dec 16, 2029compositionUS 79195983.3y
  • Dec 16, 2029compositionUS 79195983.3y
  • Dec 16, 2029compositionUS 79195983.3y
  • Sep 21, 2028patentUS 8221786*PED2.1y
  • Sep 21, 2028patentUS 8221786*PED2.1y
  • Sep 21, 2028patentUS 8361972*PED2.1y
  • Sep 21, 2028patentUS 8361972*PED2.1y
  • Sep 21, 2028patentUS 8716251*PED2.1y
  • Sep 21, 2028patentUS 8716251*PED2.1y
  • Sep 21, 2028patentUS 8716251*PED2.1y
  • Sep 21, 2028patentUS 8716251*PED2.1y
  • Sep 21, 2028patentUS 8716251*PED2.1y
  • Sep 21, 2028patentUS 8716251*PED2.1y
  • Mar 21, 2028formulationUS 82217861.6y
  • Mar 21, 2028formulationUS 82217861.6y
  • Mar 21, 2028method-of-use (U-493)US 83619721.6y
  • Mar 21, 2028method-of-use (U-493)US 83619721.6y
  • Mar 21, 2028formulationUS 87162511.6y
  • Mar 21, 2028formulationUS 87162511.6y
  • Mar 21, 2028formulationUS 87162511.6y
  • Mar 21, 2028formulationUS 87162511.6y
  • Mar 21, 2028formulationUS 87162511.6y
  • Mar 21, 2028formulationUS 87162511.6y
  • Dec 20, 2027patentUS 8501698*PED1.3y
  • Dec 20, 2027patentUS 8501698*PED1.3y
  • Dec 20, 2027patentUS 8501698*PED1.3y
  • Dec 20, 2027patentUS 8501698*PED1.3y
  • Dec 20, 2027patentUS 8501698*PED1.3y
  • Dec 20, 2027patentUS 8501698*PED1.3y
  • Jun 20, 2027formulationUS 8501698309d
  • Jun 20, 2027formulationUS 8501698309d
  • Jun 20, 2027formulationUS 8501698309d
  • Jun 20, 2027formulationUS 8501698309d
  • Jun 20, 2027formulationUS 8501698309d
  • Jun 20, 2027formulationUS 8501698309d
  • Apr 4, 2026patentUS 6515117*PED
  • Apr 4, 2026patentUS 6515117*PED
  • Apr 4, 2026patentUS 6515117*PED
  • Apr 4, 2026patentUS 6515117*PED
  • Apr 4, 2026patentUS 6515117*PED
  • Apr 4, 2026patentUS 6515117*PED
  • Oct 4, 2025compositionUS 6515117
  • Oct 4, 2025compositionUS 6515117
  • Oct 4, 2025compositionUS 6515117
  • Oct 4, 2025compositionUS 6515117
  • Oct 4, 2025compositionUS 6515117
  • Oct 4, 2025compositionUS 6515117

News(0)

no news has mentioned this drug yet

brand
DAPAGLIFLOZIN
generic
DAPAGLIFLOZIN
indication
Type 2 Diabetes
phase
marketed
Data sources
openFDA · ClinicalTrials.gov
last refreshed 49m ago
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