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Effects of Rapamycin on multiple Sclerosis treatment

Effects of Rapamycin on the gene expression of FoxP3 and GARP in CD4+CD25+FoxP3 Treg cells and evaluation of Tregs number and function in Multiple Sclerosis

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012092510936N1
Enrollment
8
Registered
2015-01-08
Start date
2012-11-09
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

relapsing remitting multiple sclerosis. Demyelinating diseases of the central nervous system

Interventions

FDA approved drug (Rapamycin) administrated to the patients, 2 mg daily for 6 months.
Treatment - Drugs
FDA approved drug (Rapamycin) administrated to the patients, 2 mg daily for 6 months

Sponsors

Vice-chancellor of Research and Technology, Isfahan University of Medical Sciences, Isfahan, Iran
Lead Sponsor
Charity
Collaborator
The researcher
Collaborator

Eligibility

Sex/Gender
All
Age
24 Years to 27 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Relapsing- Remitting MS; MRI records that proved the existence of demyelination; 0-6 expanded disability status scale (EDSS); lack of response to ß interferon or glatiramer acetate; stopping ß interferon or glatiramer acetate one month before the experimentation . Exclusion criteria: primary progressive MS; history of immunosuppressive therapy; side effects of the drug; steroid therapy in the last one month; any sign of infection and cancer; cardiovascular and hematological disorders; high serum cholesterol and using medication for it; history of hepatic cirrhosis or other liver diseases that require treatment; history of C and B hepatitis; active CMV infection; renal diseases which require treatment; active lung diseases, diabetes, hyperthyroidism, infection with HIV, tuberculosis; history of alcohol misuse during last 6 months; phobia from MRI (claustrophobia) and pregnant and lactating women.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reduction in plaque area and number, variation in the expesion of FOXP3 gene. Timepoint: Before and 6 months after the therapy with rapamyin. Method of measurement: MRI, real-time PCR.

Secondary

MeasureTime frame
Th1, 2 and 17 Cytokine variation. Timepoint: Before and 6 months after therapy with rapamycin. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMansour Salehi

Department of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Scie

m_salehi@med.mui.ac.ir+98 31 3792 2486

Outcome results

None listed

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