Biofrontera Ameluz Clinical Trial Results Show Significant Efficacy
Biofrontera announced results of its Phase 2b clinical trial evaluating Ameluz topical gel, 10% PDT for the treatment of moderate to severe acne vulgaris. The multicenter, randomized, double-blind study compared Ameluz and vehicle gel using two incubation times prior to illumination with the BF-RhodoLED lamp. Participants received one tube of Ameluz or vehicle gel applied to the entire face, followed by incubation and illumination with the red light. Up to three PDT treatments were administered at one-month intervals, and patients were followed up for two months after receiving the final PDT treatment. The study had co-primary endpoints, one of which looked at the relative reduction in inflammatory lesion counts. The other required an improvement of at least two grades on a 5-point modified Investigator Global Assessment scale and that the patient was rated "clear" or "almost clear". Greater improvements in both inflammatory lesion counts and mIGA scores were observed with Ameluz vs. vehicle with the 3-hour incubation regimen, identifying this as the most promising protocol for further clinical investigation in acne vulgaris. In the 3-hour per-protocol population, the Ameluz group achieved a 57.97% reduction in inflammatory lesions, compared with 36.51% in the corresponding vehicle group. For the mIGA analysis, 25% of the Ameluz treated patients met this co-primary endpoint with 21.4% of the vehicle patients achieving the same outcome. Reductions in absolute lesion counts further supported the efficacy of the 3-hour regimen. The values for inflammatory, non-inflammatory and total lesion reductions were 19.7, 23.1 and 42.7 with Ameluz vs. 15.4, 16.5 and 31.9 with vehicle. Ameluz PDT demonstrated a favorable safety profile consistent with previously reported photodynamic therapy experience. The most frequently reported treatment-related adverse events were burning sensation and pruritus, both of which were generally mild to moderate in severity. In addition, the average pain scores during the 3-hour incubation PDT treatments were modest, with the values in the Ameluz group ranging from 3.4 to 3.8, and from 2.0 to 2.1 with vehicle on an 11-point scale. Participants reported high overall satisfaction with PDT treatment. Of the patients who underwent the 3-hour Ameluz incubation, 85.7% said they would choose PDT again and 71.4% of them rated their esthetic outcome as "good" or "very good".
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- Financial Reporting Schedule: Biofrontera will announce its financial results for the year ended December 31, 2025, after the U.S. market closes on March 19, 2026, reflecting the company's commitment to financial transparency.
- Conference Call Timing: The company will host a conference call at 10:00 AM ET on the same day to discuss the financial results and provide a business update, aiming to bolster investor confidence in the company's future prospects.
- Product Focus Area: Biofrontera specializes in photodynamic therapy (PDT), commercializing the drug-device combination Ameluz® with the RhodoLED® lamp series for treating precancerous skin lesions, showcasing its expertise in dermatological treatments.
- Clinical Trial Expansion: The company is conducting clinical trials to extend the use of its products to treat non-melanoma skin cancers and moderate-to-severe acne, indicating its proactive approach to product development and market expansion potential.
- Clinical Trial Results: Biofrontera's Phase 2b study demonstrated that Ameluz® achieved a 57.97% reduction in inflammatory acne lesions with a 3-hour incubation, significantly outperforming the control group's 36.51%, indicating the treatment's potential in acne management.
- Efficacy Assessment: In the mIGA analysis, 25% of patients treated with Ameluz® met the co-primary endpoint compared to 21.4% in the vehicle group, further validating Ameluz®'s effectiveness in improving skin conditions.
- Safety and Tolerability: Ameluz® exhibited a favorable safety profile, with treatment-related adverse events primarily consisting of mild to moderate burning sensations and pruritus, and average pain scores during the 3-hour treatments ranged from 3.4 to 3.8, indicating good tolerability.
- Market Potential: Acne vulgaris is one of the most common dermatological conditions in the U.S., and Biofrontera plans to present these findings to the FDA in Q3 2026 to seek approval for Ameluz® in treating moderate to severe acne, thereby expanding its dermatology product line.
Project Overview: The BioFrontier AI initiative is set to present Phase 2 data for the Ameluz PDT treatment in Q3 2026.
Focus on Ameluz: The data presentation will specifically highlight the efficacy and outcomes of Ameluz in photodynamic therapy (PDT).
Study Overview: A Phase 2 study by BioFrontier AI demonstrates a favorable safety profile for a new treatment.
Implications for Treatment: The findings suggest potential advancements in therapeutic options based on the study's results.

Study Overview: A Phase 2 study has been conducted to evaluate the effects of a treatment on inflammatory acne lesions.
Results: The study shows a significant reduction in inflammatory acne lesions with the use of the treatment, Ameluz PDT.

Positive Phase 2 Results: BioFrontier AI has reported positive results from Phase 2 trials supporting the development of its AmeLuz® photodynamic therapy.
Targeted Condition: The therapy is aimed at treating moderate to severe acne vulgaris, indicating a potential advancement in acne treatment options.






