Biofrontera FDA Review Advances Ameluz® Dosage Expansion

Biofrontera (BFRI) has released an update to notify the public and investors about a regulation fd disclosure.

Biofrontera Inc. has announced a significant advancement with the FDA’s acceptance to review their application for increasing the dosage of their treatment, Ameluz®, from one to three tubes. This step suggests a move forward in the treatment’s regulatory process, potentially broadening its usage and marking a noteworthy development for investors and followers of the company’s progress in the healthcare market.

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For a comprehensive understanding of the announcement, you can read the full document here.