drugset / Trial / NCT02213861

Efficacy, Safety and Tolerability Study of SHAPE in IA, IB or IIA Cutaneous T-cell Lymphoma

NCT02213861 ↗

Phase 2 Unknown 60 enrolled TetraLogic Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy, safety and tolerability of SHAPE administered topically to skin lesions in patients with early-stage cutaneous T-cell lymphoma (CTCL).

Timeline

Start
2014-11
Primary completion
2016-10
Completion
2016-10

Drugs

EvaluationDrugModalityDoseRoute
Subject SHAPE Unknown 0.5 % Topical
Subject SHAPE Unknown 1 % Topical