Senolytics for Secondary Progressive MS

This study is testing if a treatment called senolytic therapy is safe and possible for people with secondary progressive multiple sclerosis (SPMS). The treatment involves taking two medicines, dasatinib and quercetin, by mouth every two weeks for three months. These medicines work by removing old, damaged cells that can cause inflammation and slow down nerve repair. The study is looking for adults aged 50-85 with SPMS whose symptoms have been getting worse and who are not currently taking certain MS medications. Researchers will be watching to see how many people stay in the study, how easy it is to recruit participants, and if there are any side effects from the medicines. Participants will be followed for one year to see the effects of the treatment.

Study design
This is an interventional study planning to enroll 30 participants. It is testing a specific drug combination.
What's involved
You would take dasatinib and quercetin by mouth every two weeks for three months. You would also be monitored for one year after joining the study.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for one year from enrollment to monitor for treatment effects.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07270120

Senolytics for Secondary Progressive MS

Not Yet Recruiting
PHASE1Ages 50–85InterventionalTreatment
Ohio State University
~30 participants
Updated 2025-12-08 on ClinicalTrials.gov
What's tested:Dasatinib and quercetin

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Participant retention rate
Measured over Baseline until 3 months
+2 more outcomes measured
Multiple Sclerosis (MS) Secondary Progressive

NCT07270120

Where you'd take part

This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Ohio State Martha Morehouse Outpatient Care

    Columbus, Ohiostudy coordinator listed

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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  • Participant retention rateBaseline until 3 months

    Participant retention rate with D+Q therapy with no more than one missed study visit

  • Recruitment feasibilityBaseline

    The number of subjects screened to identify eligible participants

  • Frequency of adverse drug effects of dasatinib and quercetinFrom baseline through study completion at 1 year

    Frequency of adverse drug effects of dasatinib and quercetin