Verrica Pharmaceuticals reported a net loss of $13.0 million for the fourth quarter of 2020. The company's NDA for VP-102 was accepted for filing by the FDA, and Torii Pharmaceutical exercised its option to acquire an exclusive license for VP-102 in Japan.
FDA accepted the resubmitted NDA for VP-102 with a PDUFA goal date of June 23, 2021.
Torii Pharmaceutical exercised its option to acquire an exclusive license agreement to develop and commercialize VP-102 in Japan.
Phase 2 CARE-1 clinical study of VP-102 in external genital warts (EGW) achieved positive topline results.
Verrica had aggregate cash, cash equivalents, and marketable securities of $65.5 million as of December 31, 2020.
Verrica anticipates its cash, cash equivalents, and marketable securities will be sufficient to support planned operations at least into the first quarter of 2022.