Senolytics for Secondary Progressive MS
Part of paid clinical trials in Columbus, Ohio.
- Sponsor
- Ohio State University
- Study ID
- NCT07270120
- Phase
- PHASE1
- Status
- Not Yet Recruiting
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Conditions
- Multiple Sclerosis (MS) Secondary Progressive
Eligibility Criteria
- Sex
- ALL
- Age
- 50 Years - 85 Years
- Healthy Volunteers
- Not accepted
Interventions
- Dasatinib and quercetin — DRUGParticipants will receive 100 mg of dasatinib and 1250 mg of quercetin orally once a day for 2 days every 2 weeks over 12 consecutive weeks
Study Details
This is a clinical trial to see whether senolytic therapy is safe and feasible for patients with secondary progressive MS and whether treatment improves physical and thinking abilities. The study seeks to enroll adults with secondary progressive MS (SPMS), aged 50-85, who are not currently taking a MS disease-modifying therapy and have noticed their MS symptoms getting worse. People who join the study will take the medicines dasatinib and quercetin by mouth every two weeks for three months. These medicines work together to remove old, damaged cells that may cause inflammation and slow the repair of nerves. Participants will also be followed for one year from enrollment to monitor for treatment effects.
Key Dates
- Start date
- Jan 15, 2026
- Status verified
- Dec 2025
- Primary completion
- Jan 15, 2027
- Completion
- Jan 15, 2028
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: TreatmentDasatinib and quercetin
Primary Outcome Measure
Participant retention rate [ Time Frame: Baseline until 3 months ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Ohio State Martha Morehouse Outpatient Care | Columbus | Ohio | 43210 | 6142934969 |
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