Alunbrig

Active Ingredient(s): Brigatinib
FDA Approved: * April 28, 2017
Pharm Company: * ARIAD
Category: Cancer

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



Alunbrig Overview

Brigatinib (INN;[1] marketed as Alunbrig) is an investigational small-molecule targeted cancer therapy being developed by ARIAD Pharmaceuticals, Inc.[2] Brigatinib acts as both a anaplastic lymphoma kinase (ALK) and epidermal growth factor receptor (EGFR) inhibitor. Brigatinib could overcome resistance to osimertinib conferred by the EGFR C797S mutation if it is combined with an anti-EGFR antibody such as cetuximab or panitumumab.[3] Contents...

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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/Brigatinib

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Possible Dosages for this and Related Drugs:

Brigatinib
  • Tablet: 180mg, 30mg, 90mg
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Alunbrig: (5 results)

Sorted by National Drug Code
  • 63020-090 Alunbrig 90 mg Oral Tablet, Film Coated by Millennium Pharmaceuticals, Inc.
  • 63020-113 Alunbrig 30 mg Oral Tablet, Film Coated by Millennium Pharmaceuticals, Inc.
  • 63020-180 Alunbrig 180 mg Oral Tablet, Film Coated by Millennium Pharmaceuticals, Inc.
  • 63020-198 Alunbrig Kit by Millennium Pharmaceuticals, Inc.
  • 76189-113 Alunbrig 30 mg Oral Tablet, Coated by Ariad Pharmaceuticals Inc.

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






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