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Efficacy, Safety and Tolerability of CG428 Cutaneous Solution on Chemotherapy Induced Alopecia; Controlled Study (ELAN) — ELAN  

Alopecia Clinical Trial

Official title:
A Randomized, Double Blind, Single Center, Controlled Study to Compare the Efficacy, Safety and Tolerability of CG 428 Cutaneous Solution With Placebo on Alopecia in Cancer Female Patients Under Chemotherapy

Clinical Trial Summary

Phase II clinical trial

Clinical Trial Description

The aim of this trial is to compare the degree of efficacy, safety and tolerability of CG 428 cutaneous solution versus placebo on prevention of chemotherapy induced alopecia (CIA) in female patients with metastatic cancer treated with selected regimens inducing alopecia. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02919735
Study type Interventional
Source Legacy Healthcare SA
Contact
Status Completed
Phase Phase 2
Start date October 2016
Completion date March 1, 2019
View Details
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