drugset / Trial / NCT04759664

LUT014 for the Reduction of Dose-Limiting Acneiform Lesions Associated With EGFRI Treatment of mCRC

NCT04759664 ↗

Phase 2 Unknown 117 enrolled Lutris Pharma Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The study evaluates the efficacy and safety of two strengths of LUT014 Gel topically applied once a day for 4 weeks, compared to placebo, in metastatic colorectal cancer (mCRC) patients who developed Grade 2 or non-infected Grade 3 EGFRI induced acneiform lesions

Timeline

Start
2021-04-12
Primary completion
2024-03
Completion
2024-05

Drugs

EvaluationDrugModalityDoseRoute
Subject LUT014 Small molecule — Topical

Indications