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Medication Combinations of Dasatinib, Quercetin, Fisetin, Temozolomide, LMP744, and Autologous TLPO Vaccine for the Treatment of Previously Treated Glioma With Residual Disease

Study acronym: Senolytics
StatusRecruiting
PhaseEarly Phase 1
Started2025-08-12
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 12 months later Sep 1, 2027 → Sep 1, 2028
See other at-risk trials from Mayo Clinic

Amendment history

2026-10-02
critical
Primary completion pushed: 2027-09-01 → 2028-09-01
Completion pushed: 2027-09-01 → 2028-09-01
2026-06-30
minor
Study Identification, Study Status, Study Description, Arms and Interventions v7
Trial arms changed: 7 → 9
InterventionsBiospecimen Collection (Procedure), Dasatinib (Drug), Fisetin (Drug), Magnetic Resonance Imaging (Procedure), Patient Observation (Other)…→Biospecimen Collection (Procedure), Dasatinib (Drug), Fisetin (Drug), Magnetic Resonance Imaging (Procedure), Patient Observation (Other)…
Study title+10 characters
Sequential Treatments orMedication Combinations Includingof Dasatinib, Quercetin, Fisetin, Temozolomide, LMP744, and/or TemozolomideAutologous TLPO Vaccine for the Treatment of Previously Treated Glioma With Residual Disease
2026-06-15
notable
Study Identification, Study Status, Study Design, Arms and Interventions, Eligibility v6
Enrollment increased: 10 → 30 participants
Trial arms changed: 6 → 7
InterventionsBiospecimen Collection (Procedure), Dasatinib (Drug), Fisetin (Drug), Fluorodopa F 18 (Drug), Magnetic Resonance Imaging (Procedure)…→Biospecimen Collection (Procedure), Dasatinib (Drug), Fisetin (Drug), Magnetic Resonance Imaging (Procedure), Patient Observation (Other)…
Eligibility criteria+1,248 characters
Inclusion Criteria - Treatment Arm (Regimens 1-8): Age ≥ 18 years Prior diagnosis of a glioma treated with ch [...] consent Willingness to return to Mayo Clinic for follow-up Inclusion Criteria - Monitoring Arm (Regimen 1 only): Age ≥ 18 years Prior diagnosis of a glioma Negative serum pregnancy test is required for persons of childbearing potential ≤ 8 days prior to registration Co-enrollment on the neuro-oncology biorepository [institutional review board (IRB) 12-00345 [...] Exclusion Criteria - Treatment Arm (Regimens 1-8): Any of the following because this study involves an agent [...] ng, gastric resection/ [...]
2026-01-23
minor
Study Status v5
Re-verified, no change to tracked fields
2025-08-21
notable
Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v4
Trial statusNot Yet Recruiting→Recruiting
Start dateestimated 2025-09-01→confirmed 2025-08-12
Study sitesdetails revised at 1 of 1 site
Show 3 earlier versions
2025-08-15
minor
Study Identification, Study Status v3
Start date2025-11-01→2025-09-01
2025-07-15
minor
Study Status v2
Start date2025-07-01→2025-11-01
2025-06-16
minor
Study Status, Sponsor/Collaborators v1
Re-verified, no change to tracked fields
2025-06-09
minor
Original filing
1,015 trials monitored
See 115 trials at risk
666 trials monitored
See 38 trials at risk
This early phase I trial tests the safety, side effects and how well medication combinations of dasatinib, quercetin, fisetin, temozolomide, LMP744, and autologous tumor lysate particle only (TLPO) vaccine 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. LMP744 works by interfering with a protein that tumor cells use to copy and repair their DNA. By blocking this repair process, the drug causes DNA damage so that tumor cells cannot survive. The autologous TLPO vaccine is made using material from a patient's own tumor. It delivers the tumor material to immune cells so they can learn to recognize and attack the cancer. Giving medication combinations of dasatinib, quercetin, fisetin, temozolomide, LMP744, and autologous TLPO vaccine may be safe, tolerable and/or effective in treating patients with previously treated glioma with residual disease.
Trial Details
NCT Number NCT07025226
Lead Sponsor Mayo Clinic
Conditions Glioma
Enrollment 30 participants
Start Date 2025-08-12
Primary Completion 2028-09-01 (estimated)
Study Completion 2028-09-01 (estimated)
Updated on ClinicalTrials.gov 2026-10-01