Dapagliflozin - AstraZeneca
Alternative Names: Andatang; AZ-dapagliflozin; BMS-512148; BMS-dapagliflozin; BMS/AZ-Dapagliflozin; DAPA; Dapagliflozin-AstraZeneca; Dapagliflozin-propanediol; Farxiga; Forxiga; OxraLatest Information Update: 05 Sep 2025
At a glance
- Originator Bristol-Myers Squibb
- Developer AstraZeneca; AstraZeneca KK; Bayer; Bristol-Myers Squibb; Novo Nordisk Foundation; Ono Pharmaceutical; University Medical Center Groningen; Uppsala University
- Class Anti-ischaemics; Antihyperglycaemics; Antivirals; Benzhydryl compounds; Cardiovascular therapies; Chlorobenzenes; Glucosides; Heart failure therapies; Hepatoprotectants; Obesity therapies; Pyrans; Small molecules; Urologics
- Mechanism of Action Sodium-glucose transporter 2 inhibitors
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Marketed Cardiovascular disorders; Chronic heart failure; Renal failure; Type 1 diabetes mellitus; Type 2 diabetes mellitus
- Phase III COVID 2019 infections; Heart failure; Myocardial infarction
- Phase II Kidney disorders; Liver cirrhosis; Obesity; Prediabetic state
Most Recent Events
- 05 Sep 2025 AstraZeneca completes a phase I DAPAG-02-23 bioequivalence study (In volunteers) in Romania (CTIS2023-506408-18-00)
- 09 May 2025 AstraZeneca completes the phase-II MIRO-CKD trial for Renal failure (Treatment-experienced) in USA, Austria, Brazil, Bulgaria, Canada, China, Italy, Japan, Malaysia, Poland, Spain, Taiwan, Turkey, United Kingdom and Vietnam (PO), (NCT06350123)
- 09 Sep 2024 Pharmacodynamics, efficacy and adverse events data from phase III T2NOW trial for Type 2 diabetes mellitus presented at the 60th Annual Meeting of the European Association for the Study of Diabetes (EASD-2024)