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Clinical Trial Summary

The primary objective of the study is to evaluate at Day 1 Cycle 2, the detection sensitivity of the urinary monoclonal component on a spot urine sample, compared to the reference measurement on 24-hour urine, in patients with Multiple Myeloma.


Clinical Trial Description

To evaluate the detection sensitivity of the urinary monoclonal component on a spot urine sample, compared to the reference measurement on 24-hour urine, in Multiple Myeloma patients. 300 evaluable patients are required. For each of them, both spot urine sample and 24h urine sample will be collected at Cycle1 Day1, Cycle 2 Day 1 and Cycle 4 Day 1. The detection of urine monoclonal component will be performed by urine protein electrophoresis (quantitative) and urine immunofixation (qualitative). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05208086
Study type Observational
Source Intergroupe Francophone du Myelome
Contact amandine huguet
Phone 0531156338
Email [email protected]
Status Not yet recruiting
Phase
Start date February 2022
Completion date July 2025

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