FDA Approval and Launch of VYKAT XR
FDA approved VYKAT XR for hyperphagia in Prader-Willi syndrome, and the commercial launch followed swiftly with patients receiving treatment ahead of schedule.
Strong Initial Launch Metrics
268 patient start forms received within 29 business days and 131 unique prescribers engaged, indicating strong initial interest and awareness.
Sufficient Financial Reserves
The company ended the quarter with $290 million in cash and believes it has sufficient funds to reach cash flow breakeven, with an additional $75 million available through a loan agreement.
Positive Payer and Market Feedback
Positive feedback from payers regarding the VYKAT XR value proposition, and anticipation of broad payer coverage in the U.S.