drugset / Trial / NCT02360358

Autologous Skin Substitute for Chronic Leg/Foot Ulcers.

NCT02360358 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

A prospective, multicenter, randomised controlled phase II study in which patients with therapy resistant (arterio-) venous leg/foot ulcers are treated with Tiscover® (test group) or with AS210 (control group) to determine the safety and relative efficacy of both products.

Timeline

Start
2012-08
Primary completion
2015-12
Completion
2015-12

Outcome

Outcome not reported

Stopped: “slow inclusion”

Drugs

EvaluationDrugModalityDoseRoute
Subject Tiscover Cell therapy — Topical

Indications