Zurich-Schlieren, Switzerland, September 10, 2020. TOPADUR Pharma AG, a biopharmaceutical start-up company today announces dosing of first healthy subjects in Phase 1 clinical trial evaluating the safety and tolerability of TOP-N53, a first-in-class wound healing drug candidate.TOP-N53 locally applied, increases microcirculation and induces the formation of new blood vessels.TOP-N53 has demonstrated unprecedented potency and efficacy in preclinical models. “We are very positive it will address an important need for patients with non-healing cutaneous wounds exemplified by diabetic foot ulcer (DFU) and digital ulcers (DU)“, said Reto Naef, Chairman of the Board of Directors and CEO at TOPADUR Pharma AG. The Phase 1 clinical trial will evaluate the safety and tolerability of single ascending doses of TOPN53 in healthy subjects. "The enrollment of the first subjects in this trial is a major event in the clinical development program for this promising drug candidate," commented Dr. Naef. "If successful, the trial will provide important validation for our innovative approach to treat debilitating and rare wound healing diseases."
TOPADUR announces the completion of Phase 1 dose escalation study of TOP-N53, a first-in-class wound healing drug candidate.
Read moreTOP-N53: A Clinical Drug Candidate for the Treatment of Non-healing Wounds.
Read moreThe European Patent Office granted a patent covering the lead drug candidate, TOP-N53 used for the treatment of chronic wounds.
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