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NCT07025226 · ClinicalTrials.gov registry record · Early Phase 1

Sequential Treatments or Combinations Including Dasatinib, Quercetin, Fisetin and/or Temozolomide for the Treatment of Previously Treated Glioma With Residual Disease

A Early Phase 1 study of Glioma, sponsored by Mayo Clinic.

Recruiting
Registry status
Early Phase 1
Development phase
10
Enrollment target
1
Study location

NCT07025226: Recruiting Early Phase 1 study of Glioma, sponsored by Mayo Clinic.

NCT07025226 is a Early Phase 1 study of Glioma that is actively recruiting participants, run by Mayo Clinic. The registered enrollment target is 10 participants, below the 210-participant average among 87 other Glioma trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07025226, a Early Phase 1 study of Glioma, is actively recruiting participants, sponsored by Mayo Clinic.

RECRUITING
Registry status
Early Phase 1
Development phase
10 participants
Enrollment target
1
Study location

Study 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.

Primary Outcome

Will evaluate feasibility of serially screening multiple candidate therapies or combinations based on individualized empiric biological feedback from biospecimens and imaging. This will be measured as the percentage of patients successfully completing 3 cycles of drug administration (study visits). A cycle is 35 +/- 7 days. Regimen will be considered feasible if at least 2/3 of patients can achieve this target.

Conditions Studied

Interventions

  • PROCEDURE Biospecimen Collection
  • PROCEDURE Magnetic Resonance Imaging
  • DRUG Dasatinib
  • DRUG Fisetin
  • DRUG Fluorodopa F 18

Study Locations (1)

Minnesota

  • Mayo Clinic in Rochester - Rochester

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2025-08-12
Est. Completion 2027-09-01
Phase Early Phase 1
Mayo Clinic

2,844 total trials

What NCT07025226 shows while recruiting

NCT07025226 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 210-participant average among 87 other Glioma trials with a reported enrollment target (95% lower).

The record links to 1 condition, with Glioma appearing as the primary indexed condition, and to 5 interventions - of which Biospecimen Collection is the first listed.

NCT07025226 reports a single indexed study location in Minnesota.

Frequently Asked Questions

What is clinical trial NCT07025226 about?

NCT07025226 is a clinical study titled "Sequential Treatments or Combinations Including Dasatinib, Quercetin, Fisetin and/or Temozolomide for the Treatment of Previously Treated Glioma With Residual Disease". 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 att...

What is the current status of trial NCT07025226?

This trial is currently recruiting. It is a Early Phase 1 study. The enrollment target is 10 participants. The study started on 2025-08-12. Estimated completion is 2027-09-01.

What conditions does trial NCT07025226 study?

This clinical trial studies the following conditions: Glioma.

What interventions are being tested in trial NCT07025226?

The interventions under investigation include: Biospecimen Collection (PROCEDURE), Magnetic Resonance Imaging (PROCEDURE), Dasatinib (DRUG), Fisetin (DRUG), Fluorodopa F 18 (DRUG).

Who is sponsoring clinical trial NCT07025226?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07025226 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Glioma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07025226's enrollment target sits among peer trials

10 79th of 87 higher than 6 of 87 other Glioma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Glioma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07025226, the US trial registry maintained by the National Library of Medicine. NCT07025226 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.