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Collection of Blood Samples From Patients With Relapsing MS Who Developed ITP After Receiving Lemtrada — LEMTRADA-ITP  

Multiple Sclerosis Clinical Trial

Official title:
Collection of Blood Samples From Patients With Relapsing Forms of Multiple Sclerosis (RMS) Who Have Developed Immune Thrombocytopenic Purpura (ITP) After LEMTRADA® Treatment

Clinical Trial Summary

Primary Objective: To collect blood samples in a new cohort of Relapsing Forms of Multiple Sclerosis (RMS) participants who had developed immune thrombocytopenic purpura (ITP) after LEMTRADA treatment, for future Deoxyribonucleic acid (DNA) analysis as part of a global biomarker project assessing pre-identified candidate single nucleotide polymorphisms (SNPs) associated to the development of ITP after LEMTRADA treatment in RMS participants.

Clinical Trial Description

One to 70 days, as screening and inclusion visit(s) were performed the same day or on separate days with a maximum timeframe of 30 days apart. One visit was required for blood draw. However, if a second visit occured, it took place within 40 days of the first visit. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03784898
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 4
Start date February 8, 2019
Completion date December 11, 2019
View Details
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