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Efficacy of Topical TolaSure on Acute Induced Wounds in Healthy Participants

Wound Healing Clinical Trial

Official title:
A Phase II, Closed Label, Randomized, Double Blind Study for the Treatment of Acute Induced Wounds With TolaSure Gel, 5% w/w in Healthy Volunteers

Clinical Trial Summary

TolaSure is a topical gel for the promotion of accelerated wound healing. This phase II study will primarily assess the efficacy of TolaSure when applied to skin wounds created by punch biopsy in healthy participants. Safety, cutaneous tolerability, wound pain control, and quality of healing will also be assessed. A total of 80 healthy volunteers, males and females ages 18 years or older, will be enrolled. Subjects will be monitored for safety and efficacy until wound closure (estimation about 8 weeks) following topical administration of TolaSure.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04088357
Study type Interventional
Source BioMendics, LLC
Contact
Status Completed
Phase Phase 2
Start date August 26, 2019
Completion date April 22, 2020
View Details
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