News about Viatris

The U.S. FDA has approved Viatris' RYZUMVI (phentolamine ophthalmic solution 0.75%) for treating presbyopia, the age-related loss of near focusing ability, in adults. The drug was already approved in the U.S. for pharmacologically induced mydriasis, and the new approval expands its use. Viatris holds exclusive U.S. commercialization rights under a licensing deal with Opus Genetics and is exploring a U.S. partner to commercialize RYZUMVI for presbyopia. The most common ocular side effects reported for presbyopia were conjunctival hyperemia (21%) and instillation site irritation (16%), and the drug is not recommended for patients with active ocular inflammation.