clinical trial · NCT04468165
Effectiveness and Safety of Generic Delayed-Release Dimethyl Fumarate (Sclera® or Marovarex ®, Hikma) in Routine Medical Practice in the Treatment of Relapsing-Remitting Multiple Sclerosis in MENA Region
Relapsing Remitting Multiple SclerosisDimethyl Fumarate (DMF)
brief 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
started
Feb 23, 2021
primary completion
Jul 20, 2023
completion
Jul 20, 2023
last updated
Sep 22, 2023
detailed 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.
sourced from ClinicalTrials.gov · pharmadog mirrors structured fields, not the full protocol