Effectiveness and Safety of Ocrelizumab in Primary Progressive Multiple Sclerosis among Iraqi Patients

Dr. Ismael Raje Albayati , Dr. Anmar Oday Hatem

Abstract

Background Multiple sclerosis disorder altering agents are classify into two groups: drugs with medium effectiveness, also known as platform therapies, and high efficacy agent treatments (HEATs). Ocrelizumab (Ocrevus®), a humanized anti-CD20 monoclonal antibody given through veinous line, is approved for adults in deteriorating forms of multiple sclerosis or primary progressive multiple sclerosis.


Aim: The study aims to evaluate Effectiveness and safety of (Ocrelizumab) in Primary Progressive Multiple - Sclerosis among Iraqi patients.


Method: A multi centered, prospective study conducted in 3 hospitals in Iraq. A study analyzed clinical and MRI data in two visits over 6 months period.


Results: A study compromised 151 participants demonstrate 51% males while (49%) females with mean age 41±10; most patients taken (2) doses. Average of Expanded Disability Status Scale score of patients significantly increased from 4.851 to 5.026 with 34 (22.5%) confirmed disability progression. There was significant reduction in the progression index from 1.030 to 0.909 between two visits. Brain MRI experienced a substantial reduction in the number of T2 lesions from 8 to 7 with stable spinal MRI lesions. Ocrelizumab was well tolerated with most common adverse events were infusion related and 99% of them classified as mild.


Conclusion: Ocrelizumab appears effective in delaying the progression of the illness and lowering the development of MRI lesions in people with Multiple - Sclerosis.

Full Article

Generated from XML file

Authors

Dr. Ismael Raje Albayati
Dr. Anmar Oday Hatem
Albayati , D. I. R., & Oday Hatem, D. A. (2025). Effectiveness and Safety of Ocrelizumab in Primary Progressive Multiple Sclerosis among Iraqi Patients. World of Medicine : Journal of Biomedical Sciences, 2(3), 86–91. Retrieved from https://wom.semanticjournals.org/index.php/biomed/article/view/322
Copyright and license info is not available

Article Details