Sitagliptin in Recurrent/Progressive Grade 4 Glioma
Part of paid clinical trials in Iowa City, Iowa.
- Sponsor
- Kailin Yang, MD, PhD
- Study ID
- NCT07541781
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Glioblastoma
- Glioma
- Grade 4 Malignant Glioma of Brain (Disorder)
- Recurrent Glioblastoma
- Recurrent Glioma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Sitagliptin — DRUGSitagliptin, PO dose to be determined by Phase I dose de-escalation, cycle length 28 days. Treatment until progression.
- Bevacizumab — BIOLOGICALBevacizumab, IV, 10 mg/kg days 1 and 15 every 28 days, until progression.
Study Details
Sitagliptin, when combined with standard-of-care drug bevacizumab, is being tested to 1) find out if it is effective at treating gliomas that have returned or progressed after treatment, and 2) find out what the highest dose of sitagliptin is appropriate to give when combined with bevacizumab.
Key Dates
- First listed
- Apr 21, 2026
- Start date
- Jun 11, 2026
- Status verified
- Jun 2026
- Primary completion
- Jun 11, 2029
- Completion
- Jun 11, 2030
Study Design
- Enrollment
- 45 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Standard of care Bevacizumab in addition to SitagliptinPhase I: Bevacizumab in combination with Sitagliptin Phase Ib: a standard 3+3 design and dose de-escalation will be used to determine the maximal tolerated dose (MTD) of sitagliptin in combination with bevacizumab on non-surgical patients with recurrent GBM Pilot: 12 patients with recurrent GBM, will receive pre-operative treatment with sitagliptin for at least 5 days at the MTD determined in phase 1b. These patients will then undergo surgical resection of the tumor. All patients will receive postoperative sitagliptin in addition to standard-of-care bevacizumab
Primary Outcome Measure
Phase Ib: Dose-limiting toxicities as measured by CTCAE v5.0 [ Time Frame: First day of treatment through completion of cycle 2 of therapy (each cycle is 28 days) ]
Central Contacts
- Kailin Yang, MD, PhD+1 319 356 3630
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Iowa Health Care | Iowa City | Iowa | 52242 | Kailin Yang, MD, PhD (PRINCIPAL_INVESTIGATOR) |
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