Hemlibra

Active Ingredient(s): Emicizumab
FDA Approved: * November 16, 2017
Pharm Company: * GENENTECH INC
Category: Blood Clotting (Hemostasis)

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

Hemlibra Overview

Emicizumab (trade name Hemlibra) is a humanized monoclonal antibody for the treatment of haemophilia A, developed by Chugai (a subsidiary of Roche).[1] A Phase I clinical trial found that it was well tolerated by healthy subjects.[2] In November 2017, it was approved by the US FDA for treatment of haemophilia A patients who had developed resistance to other treatments.[3] It was subsequently approved by the US FDA in April 2018 under the breakth...

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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/Emicizumab

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NDC Database Records for Hemlibra: (4 results)

Sorted by National Drug Code

• 50242-920 Hemlibra 30 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.
• 50242-921 Hemlibra 150 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.
• 50242-922 Hemlibra 150 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.
• 50242-923 Hemlibra 150 mg/ml Subcutaneous Injection, Solution by Genentech, Inc.

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