Idhifa

Active Ingredient(s): Enasidenib
FDA Approved: * August 1, 2017
Pharm Company: * CELGENE CORP
Category: Cancer

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Idhifa Overview

Enasidenib (INN; trade name Idhifa) is a drug used to treat relapsed or refractory acute myeloid leukemia in people with specific mutations of the isocitrate dehydrogenase 2 (IDH2) gene, determined by an FDA-approved IDH2 companion diagnostic test.[1] It is an inhibitor of IDH2. It was developed by Agios Pharmaceuticals and is licensed to Celgene for further development. Contents 1 Medical use 2 Adverse effects 3 Pharmacology 4 History 5 References Medical use Enaside...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Enasidenib

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NDC Database Records for Idhifa: (2 results)

Sorted by National Drug Code

• 59572-705 Idhifa 50 mg Oral Tablet, Film Coated by Celgene Corporation
• 59572-710 Idhifa 100 mg Oral Tablet, Film Coated by Celgene Corporation

Other drugs which contain Enasidenib or a similar ingredient: (1 result)

• ENASIDENIB