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Fitusiran
go.drugbank.com/drugs/DB15002ApprovedInvestigational[L52860] Fitusiran was first approved by the FDA on March 28, 2025, as routine prophylaxis therapy to prevent or reduce the frequency of bleeding episodes associated with hemophilia A or B.
Azathioprine
go.drugbank.com/drugs/DB00993ApprovedInvestigational[L11214] Azathiprine was granted FDA approval on 20 March 1968.[L11214]
Products: AZATIOPRINA GENERICSTiludronic acid
go.drugbank.com/drugs/DB01133ApprovedVet approvedWithdrawn[A202235] Tiludronic acid was granted FDA approval on 7 March 1997.[L4763]
Insulin icodec
go.drugbank.com/drugs/DB16693ApprovedInvestigational[L51078]The US FDA subsequently approved insulin icodec in March 2026 for use as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus. [L56102] … [L50758,A263818] Insulin icodec was approved by Health Canada in March 2024 for the treatment of adult patients with type 1 or 2 diabetes mellitus,[L50758] and was subsequently approved by the EMA in
Premature Ventricular Contraction (PVC)
go.drugbank.com/conditions/DBCOND0090285Drugs: BisoprololSynonyms: Ventricular premature complex, Ventricular ectopic complexLeniolisib
go.drugbank.com/drugs/DB16217ApprovedInvestigationalThe FDA approved leniolisib on March 24, 2023, making it the first treatment for activated phosphoinositide 3-kinase delta syndrome (APDS).
Basement membrane-specific heparan sulfate proteoglycan core protein
go.drugbank.com/bio_entities/BE0001031TargetHumansIntegral component of basement membranes. Component of the glomerular basement membrane (GBM), responsible for the fixed negative electrostatic membrane charge, and which provides a barrier which is both size- and charge-selective. It se...
Polypeptides: Basement membrane-specific heparan sulfate proteoglycan core proteinEntecavir
go.drugbank.com/drugs/DB00442ApprovedInvestigationalFood and Drug Administration (FDA) in March 2005.
Almonertinib
go.drugbank.com/drugs/DB16640ApprovedInvestigational[A231859] On March 19, 2020, almonertinib was approved in China for the treatment of EGFR T790M+ non-small cell lung cancer.[A231864] Almonertinib was also approved by the EMA on February 20, 2026.