Commercialization OpportunitiesFDA-approval and launch of phentolamine (ophthalmic solution 0.75%) Ryzumvi reflects the beginning of commercial efforts from the established development and commercialization global license agreement with partner Viatris Inc.
Gene Therapy Market PotentialGene therapy for rare diseases faces limited competition and may charge up to $850k per patient, similar to LUXTURNA.
Ryzumvi Development And Financial StrategyOcuphire will manage the trials with partner Viatris, who will reimburse Ocuphire for agreed-to budgeted costs related to Ryzumvi development through FDA approval.