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Clinical Trial Summary

The aim of the study is to evaluate the safety and tolerability of PDT for treatment of mild to severe actinic keratosis on the face and scalp in the expanded treatment field using 3 tubes of BF-200 ALA 10% gel (Ameluz®) in conjunction with the BF-RhodoLED® XL PDT lamp.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05060237
Study type Interventional
Source Biofrontera Bioscience GmbH
Contact Corinna Zogel, Dr.
Phone +49 214 3119772207
Email [email protected]
Status Not yet recruiting
Phase Phase 1
Start date November 2021
Completion date March 2022

See also
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Completed NCT00989313 - A Long Term Follow up Study of Patients Who Have Complete Clearance of Their Actinic Keratosis (AK) Lesions at the Day 57 Visit in the PEP005-028 Study Phase 3
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Recruiting NCT03684772 - Topical Ionic Contra-Viral Therapy in Actinic Keratosis Phase 2
Completed NCT02878382 - Potential Impact of Patient Vitamin D Status in AK Response to MAL-PDT N/A