Tags: multiple sclerosis | fda | viatris | mapi pharma | injection | long-acting | once-a-month

FDA Declines to Approve Multiple Sclerosis Injection

illustration of head and brain and nerves
(Dreamstime)

Monday, 11 March 2024 07:35 AM EDT

The U.S. FDA has declined to approve Viatris and Mapi Pharma's once-a-month injection for treating relapsing forms of multiple sclerosis (MS), the companies said on Monday.

The companies were reviewing the content of the health regulator's complete response letter and would soon determine the appropriate next steps, they said.

The injection, GA Depot, is a long-acting injection version of glatiramer acetate, which was approved for relapsing forms of MS under brand name Copaxone, manufactured by Teva Pharmaceutical Industries.

MS is a neurological disease in which the immune system attacks brain cells, causing motor disabilities. It affects about 400,000 people in the United States, according to the National Institutes of Health.

Relapsing MS is a type of the disease where the symptoms appear sporadically, in the form of attacks. This is followed by a period of disease inactivity and weeks, months, or even years may pass before another attack occurs. 

© 2025 Thomson/Reuters. All rights reserved.


Health-News
The U.S. FDA has declined to approve Viatris and Mapi Pharma's once-a-month injection for treating relapsing forms of multiple sclerosis (MS), the companies said on Monday. The companies were reviewing the content of the health regulator's complete response letter and would...
multiple sclerosis, fda, viatris, mapi pharma, injection, long-acting, once-a-month, relapsing
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2024-35-11
Monday, 11 March 2024 07:35 AM
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