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Clinical Trial Summary

The aim of this study is to assess the efficacy of range of dermo-cosmetic products (hand/feet serum, nail strengthening solution nail strengthening solution, dissolving oil and gloves/slippers) based on natural products and designed for cancer patients)on bispecific Ac-induced skin and nail toxicity in MM patients treated with anti-CD3xGPRC5D bispecific antibodies. The effects of supportive care products will be studied as a preventive measure in patients starting treatment with bispecific Ac and as a curative measure in patients undergoing treatment. Patients will be able to apply the products directly at home according to the study schedule, and a skin and nail toxicity skin and nail toxicity will be performed each time the patient comes for administration of bispecific Ac. Follow-up will be for a total of 6 months (or less if progression occurs earlier), and patients will be asked to complete a quality-of-life questionnaire at protocol inclusion and after 1 month and 6 months of supportive care.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06418750
Study type Interventional
Source Nantes University Hospital
Contact Cyrille Touzeau
Phone 02 53 48 24 05
Email cyrille.touzeau@chu-nantes.fr
Status Not yet recruiting
Phase N/A
Start date July 2024
Completion date June 2026

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