drugset / Trial / NCT05165069

The Efficacy and Safety of Mecobalamin in the Prevention of Capecitabine Induced Hand Foot Syndrome

NCT05165069

Phase 3 Active not recruiting 234 enrolled Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
RandomizedParallel-groupQuadruple-blindPrevention

Summary

A multicenter, randomized, placebo-controlled, double-blind, phase III clinical trial will be conducted to explore the efficacy and safety of mecobalamin in the prevention of 2/3 HFS in patients with early breast cancer. 234 patients will be enrolled and will be randomized into mecobalamin group and placebo group at the ration of 1:1. The incidence of grade 2 / 3 HFS in the experimental group and the control group will be observed. This study is expected to provide evidence for clinical prevention of hand foot syndrome, improve clinical treatment guidelines for early breast cancer, and provide reference for other antitumor drugs for hand foot syndrome.

Timeline

Start
2022-01-01
Primary completion
2024-08-22
Completion
2030-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject methylcobalamin Small molecule 0.5 mg Oral

Indications