Biofrontera Inc. and Biofrontera AG discuss potential company combination and license agreement revisions. Terms remain undisclosed.
Quiver AI Summary
Biofrontera Inc. announced on June 11, 2025, that it is in discussions with Biofrontera AG regarding a potential merger or changes to their existing licensing and supply agreement. This could involve transferring certain rights from Biofrontera AG to Biofrontera Inc. and lowering the transfer price for licensed products in the U.S. However, no specific terms have been agreed upon yet, and any potential agreements are contingent on further negotiations. Biofrontera Inc. specializes in photodynamic therapy for dermatological conditions, marketing products such as Ameluz® in combination with the RhodoLED® lamp series for treating pre-cancerous skin lesions and is exploring additional applications for its products. The release also includes various forward-looking statements about the company’s prospects and the challenges it may face, emphasizing that actual results could vary significantly.
Potential Positives
- Potential for a beneficial combination with Biofrontera AG which could enhance operational capabilities and product offerings.
- Negotiations for a possible adjustment of the license and supply agreement might lead to reduced costs for Biofrontera Inc.'s licensed products in the US.
- Continued focus on expanding the use of Ameluz® for treating various skin conditions, indicating ongoing commitment to innovation and market growth.
Potential Negatives
- The potential transfer of rights and obligations from Biofrontera AG to Biofrontera Inc. may indicate uncertainty regarding the stability and terms of their current license and supply agreement.
- The ongoing negotiations could imply that there are unresolved issues between Biofrontera AG and Biofrontera Inc., which may affect the operational and strategic outlook of the company.
- The acknowledgment of various risks and uncertainties in the company's forward-looking statements highlights potential challenges that could hinder progress and profitability.
FAQ
What is the main focus of Biofrontera Inc.?
Biofrontera Inc. specializes in the development and commercialization of photodynamic therapy (PDT) for dermatological conditions.
What recent announcement was made by Biofrontera Inc.?
Biofrontera Inc. confirmed ongoing negotiations with Biofrontera AG regarding a possible company combination or license agreement adjustments.
What is Ameluz® and its purpose?
Ameluz® is a drug-device combination used for treating actinic keratosis and pre-cancerous skin lesions with PDT.
What risks might affect Biofrontera’s future performance?
Risks include supply chain disruptions, clinical trial outcomes, and changes in healthcare provider practices regarding reimbursement.
How can I stay updated on Biofrontera Inc.?
You can visit their website at www.biofrontera-us.com and follow them on LinkedIn and Twitter for updates.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
Full Release
WOBURN, Mass., June 11, 2025 (GLOBE NEWSWIRE) -- Biofrontera Inc. (Nasdaq: BFRI), a biopharmaceutical company focused on the development and commercialization of photodynamic therapy (PDT), confirms a disclosure by the Management Board of Biofrontera AG on June 10, 2025, according to which the two companies are in negotiations regarding a possible combination of the two companies or an adjustment of the license and supply agreement between them. The latter could result in the transfer of certain rights and obligations from Biofrontera AG to Biofrontera Inc. and a reduction in the transfer price for Biofrontera Inc.’s licensed products sold in the US.
The terms of any such agreement or agreements have not yet been established and are subject to numerous conditions, including the negotiation and execution of definitive agreements between the companies.
About Biofrontera Inc.
Biofrontera Inc. is a U.S.-based biopharmaceutical company specializing in the treatment of dermatological conditions with a focus on PDT. The Company commercializes the drug-device combination Ameluz ® with the RhodoLED ® lamp series for PDT of AK, pre-cancerous skin lesions which may progress to invasive skin cancers. The Company performs clinical trials to extend the use of the products to treat non-melanoma skin cancers and moderate to severe acne. For more information, visit www.biofrontera-us.com and follow Biofrontera on LinkedIn and Twitter .
Forward-Looking Statements
Certain statements in this press release may constitute “forward-looking statements” within the meaning of the United States Private Securities Litigation Reform Act of 1995, as amended. These statements include, but are not limited to, statements relating to Biofrontera's commercial opportunities and the commercial success of its licensed products. We have based these forward-looking statements on our current expectations and projections about future events. Nevertheless, actual results or events could differ materially from the plans, intentions and expectations disclosed in, or implied by, the forward-looking statements we make. These risks and uncertainties, many of which are beyond our control, include, but are not limited to: the impact of any extraordinary external events; any changes in the Company’s relationship with its licensors; the ability of the Company’s licensors to fulfill their obligations to the Company in a timely manner; the Company’s ability to achieve and sustain profitability; whether the current global disruptions in supply chains will impact the Company’s ability to obtain and distribute its licensed products; changes in the practices of healthcare providers, including any changes to the coverage, reimbursement and pricing for procedures using the Company’s licensed products; the uncertainties inherent in the initiation and conduct of clinical trials; availability and timing of data from clinical trials; whether results of earlier clinical trials or trials of Ameluz ® in combination with BF-RhodoLED and/or RhodoLED XL in different disease indications or product applications will be indicative of the results of ongoing or future trials; uncertainties associated with regulatory review of clinical trials and applications for marketing approvals; whether the market opportunity for Ameluz in combination with BF- RhodoLED and/or RhodoLED XL is consistent with the Company’s expectations; the Company’s ability to retain and hire key personnel; the sufficiency of cash resources and need for additional financing; and other factors that may be disclosed in the Company’s filings with the Securities and Exchange Commission (the “SEC”), which can be obtained on the SEC’s website at www.sec.gov . Readers are cautioned not to place undue reliance on the forward-looking statements, which speak only as of the date on which they are made and reflect management’s current estimates, projections, expectations and beliefs. The Company does not plan to update any such forward-looking statements and expressly disclaims any duty to update the information contained in this press release except as required by law.
Contact:
Investor Relations
Andrew Barwicki
1-516-662-9461
[email protected]