Trials / Not Yet Recruiting
Not Yet RecruitingNCT05521997
Glutaminase Inhibition and Chemoradiation in Advanced Cervical Cancer
Phase II Study of Glutaminase Inhibition and Chemoradiation in Advanced Cervical Cancer
- Status
- Not Yet Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 42 (estimated)
- Sponsor
- Washington University School of Medicine · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Advanced cervical cancer patients treated with standard of care (SOC) chemoradiation plus glutaminase inhibition with telaglenastat (CB-839) will have increased progression-free survival (PFS) compared to historical rates for patients receiving SOC chemoradiation alone.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Telaglenastat | -800 mg twice per day by mouth |
| RADIATION | Radiation treatment | * Standard of care * External beam radiation therapy delivered daily 4 days a week and 1 day per week of brachytherapy. |
| DRUG | Cisplatin | * Standard of care * Weekly administration of cisplain |
Timeline
- Start date
- 2026-07-31
- Primary completion
- 2032-10-07
- Completion
- 2032-10-07
- First posted
- 2022-08-30
- Last updated
- 2026-03-13
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05521997. Inclusion in this directory is not an endorsement.