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Selumetinib granted US Breakthrough Therapy Designation in neurofibromatosis type 1

Increase font size  Decrease font size Date:2019-04-04   Views:541

AstraZeneca and MSD, Inc., Kenilworth, NJ, US (MSD: known as Merck & Co., Inc. inside the US and Canada) today announced that the US Food and Drug Administration (FDA) has granted Breakthrough Therapy Designation (BTD) for the MEK 1/2 inhibitor and potential new medicine selumetinib.

 
 
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