Biofrontera Kicks Off US Clinical Study Program for Ameluz®
Biofrontera Inc. (BFRI)
Company Research
Source: GlobeNewswire
WOBURN, MA, Nov. 16, 2021 (GLOBE NEWSWIRE) -- Biofrontera Inc. (Nasdaq: BFRI) (the “Company”), a biopharmaceutical company specializing in the commercialization of dermatological products, announced today the start of a clinical study program focused on optimizing and expanding the market positioning of its in-licensed FDA-approved prescription drug Ameluz® for photodynamic therapy (PDT) in the United States. Site initiations for two upcoming studies are currently in progress with patient recruitment to start before the end of the year. The studies are being initiated and overseen by Biofrontera AG, an affiliate of the Company. Within the scope of the license and supply agreement (LSA) between Biofrontera Inc. and Biofrontera AG and its Germany-based subsidiaries (together the “Licensor”), the Company holds the exclusive rights to market and sell Ameluz® and the PDT-lamps BF-RhodoLED® as well as its successor model BF-RhodoLED XL in the United States. Under the terms of the LSA, Bi
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BFRI
Earnings
- 11/9/23 - Beat
BFRI
Sec Filings
- 5/7/24 - Form SC
- 5/3/24 - Form 8-K
- 5/3/24 - Form S-1
- BFRI's page on the SEC website