Trials / Recruiting
RecruitingNCT07025226
Sequential Treatments or Combinations Including Dasatinib, Quercetin, Fisetin and/or Temozolomide for the Treatment of Previously Treated Glioma With Residual Disease
MC230715 Pilot Study of the Mechanistic Feedback From CNS Tumors With Latent Residual Disease to Guide Individualized Therapies
- Status
- Recruiting
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 10 (estimated)
- Sponsor
- Mayo Clinic · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This early phase I trial tests the safety, side effects and how well medication combinations of dasatinib, quercetin, fisetin and temozolomide work in treating patients with glioma for which the patient has received treatment in the past (previously treated) and for tumor cells that remain after attempts to treat the tumor have been made (residual disease). Dasatinib is in a class of medications called tyrosine kinase inhibitors. It works by blocking the action of an abnormal protein that signals tumor cells to multiply, which may help keep tumor cells from growing. Quercetin and fisetin are compounds found in plants. They have antioxidant and anti-inflammatory properties and help remove senescent cells, older or damaged cells that have stopped dividing but don't die off as they should and build up in tissues over time. Senescent cells may cause inflammation or damage to nearby healthy cells. Temozolomide is in a class of medications called alkylating agents. It works by damaging the cell's deoxyribonucleic acid (DNA) and may kill tumor cells and slow down or stop tumor growth. Giving medication combinations of dasatinib, quercetin, fisetin and temozolomide may be safe, tolerable and/or effective in treating patients with previously treated glioma with residual disease.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Biospecimen Collection | Undergo blood and CSF sample collection |
| DRUG | Dasatinib | Given PO |
| DRUG | Fisetin | Given PO |
| DRUG | Fluorodopa F 18 | Undergo 18F-DOPA-PET scan |
| PROCEDURE | Magnetic Resonance Imaging | Undergo MRI |
| OTHER | Patient Observation | Receive rest and take no treatment |
| PROCEDURE | Positron Emission Tomography | Undergo 18F-DOPA-PET scan |
| DRUG | Quercetin | Given PO |
| DRUG | Temozolomide | Given PO |
Timeline
- Start date
- 2025-08-12
- Primary completion
- 2027-09-01
- Completion
- 2027-09-01
- First posted
- 2025-06-17
- Last updated
- 2026-01-26
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT07025226. Inclusion in this directory is not an endorsement.