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Clinical trialNCT05080764CompletedPhase 2Interventional

Study to Evaluate the Safety and Efficacy of BF-200 ALA (Ameluz®) and BF-RhodoLED® in the Treatment of Moderate to Severe Acne Vulgaris With Photodynamic Therapy in Adults

SponsorBiofrontera Inc.Enrollment120Acne Vulgaris
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The aim of this study is to test the safety and efficacy of photodynamic therapy (PDT) for the medication Ameluz® performed with the PDT-lamp BF-RhodoLED® in comparison to the respective placebo treatment for moderate to severe Acne vulgaris.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

  • Mitchel P Goldman, MD

    Dermatology Cosmetic Laser Medical Associates of La Jolla, Inc.

    Principal Investigator

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

9 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • First Oc Dermatology

    Fountain Valley, California, United States

  • Cosmetic Laser Dermatology

    San Diego, California, United States

  • Dermatology Associates Pa of the Palm Beaches

    Delray Beach, Florida, United States

  • Forcare Clinical Research

    Tampa, Florida, United States

  • Delricht Research

    Baton Rouge, Louisiana, United States

  • Skin Search of Rochester, Inc

    Rochester, New York, United States

  • Clinical Research Center of the Carolinas

    Charleston, South Carolina, United States

  • Dermresearch Pa

    Austin, Texas, United States

  • Austin Institute for Clinical Research Inc.

    Pflugerville, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
10 Dec 2021
Primary completion
22 Aug 2025
Completion
7 Jan 2026
Last update posted
8 Jul 2026
Registered enrollment
120
Registry id
NCT05080764

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.