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Clinical Trial Summary

The purpose of this observational study is to evaluate the effectiveness, safety and health related quality of life of Generic DMF (Sclera® or Marovarex ®, Hikma) in patients undergoing routine clinical care for RRMS in MENA Region


Clinical Trial Description

This is an observational, multi-center, prospective, cohort study, where no visits or intervention(s) additional to the daily practice will be performed. In the study sites, patients undergoing routine clinical care for RRMS and initiated treatment with Generic DMF (Sclera® or Marovarex ®, Hikma) in accordance with the approved SPC will be followed up and assessed for a total of 12 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04468165
Study type Observational
Source Hikma Pharmaceuticals LLC
Contact
Status Completed
Phase
Start date February 23, 2021
Completion date July 20, 2023

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