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The evaluation of therapeutic effects and adverse effects of Imatinib in Secondary Progressive Multiple Sclerosis

Imatinib Treatment for Secondary Progressive Multiple Sclerosis: A Randomized Control Trial Study Assessing Clinical and Radiological Responses and adverse effects in comparison with Novanterone

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201210231584N3
Enrollment
28
Registered
2012-11-14
Start date
2012-11-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis. Multiple sclerosis (MS), also known as

Interventions

Intervention 1: Case group receives Imatinib 400 mg daily (PO). Intervention 2: Control group will receive Novanterone according to accepted guidelines.
Treatment - Drugs
Case group receives Imatinib 400 mg daily (PO)
Control group will receive Novanterone according to accepted guidelines

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: SPMS patients with relapse; EDSS between 3 and 5; age between 18 and 40 Exclusion criteria: History of other autoimmune disorder or chronic hematologic, renal, liver or infectious diseases; Pregnancy; lactation; History of HIV and Hepatitis; History of cancer especially breast tumor; History of recent herpes zoster infection; History of cytotoxic drugs consumption during recent three months; History of high dose corticosteroid during recent two months.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical signs and symptoms. Timepoint: every one month. Method of measurement: Number of relapses during six months, EDSS changes.;Adverse effect. Timepoint: every one month. Method of measurement: biochemical test, clinical examination.

Secondary

MeasureTime frame
Number of new plaques in MRI. Timepoint: six months. Method of measurement: Brain MRI with and without Gad.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammad Hossein Harirchian

Tehran University of Medical Sciences

harirchm@sina.tums.ac.ir+98 21 6119 2424

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026