Biofrontera(US:BFRI) Globenewswire·2026-02-11 14:15Core Viewpoint - Biofrontera Inc. has received FDA acceptance for its supplemental New Drug Application for Ameluz, which could expand its use to treat superficial basal cell carcinoma (sBCC) if approved, addressing a significant unmet medical need in dermatology [1][4][6]. Group 1: FDA Approval and Market Potential - The FDA has completed its review and accepted the filing of Biofrontera's sNDA for Ameluz, with a PDUFA target action date set for September 28, 2026 [1][6]. - If approved, this indication would significantly expand the Ameluz PDT platform beyond its current use for actinic keratosis, validating Biofrontera's photodynamic therapy approach [2][4]. - The potential approval would make Ameluz the first PDT photosensitizer indicated for the treatment of sBCC in the U.S., which is the most common skin cancer with approximately 3.6 million cases diagnosed annually [6][8]. Group 2: Clinical Significance and Treatment Options - Basal cell carcinoma (BCC) is prevalent in the U.S., with estimates suggesting that 10-25% of cases are of the superficial subtype, highlighting the need for effective treatment options [3][6]. - Current treatment methods often involve surgical or destructive approaches, which may not be suitable for all patients, indicating a demand for non-invasive alternatives like Ameluz PDT [3][4]. Group 3: Company Strategy and Leadership - The CEO of Biofrontera emphasized the importance of this milestone in expanding the clinical utility of Ameluz and reinforcing photodynamic therapy as a versatile platform in dermatology [4]. - The company believes that the new indication for Ameluz has the potential to significantly expand its addressable market and strengthen its position in medical dermatology [4].