Datapoint: Roche Scores FDA Nod for New Eye Drug

The FDA last week approved Roche’s Vabysmo in neovascular (or “wet” age-related) macular degeneration and diabetic macular edema, eye disorders that are among the leading causes of blindness. The drug, which is the first FDA-approved bispecific antibody for the eye, will have to face off against Regeneron’s blockbuster Eylea. For the treatment of neovascular macular degeneration, Eylea holds covered or better status for 91% of all insured lives under the medical benefit.

SOURCE: MMIT Analytics, as of 2/2/22

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AIS Health Staff

AIS Health Staff

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