Glutaminase Inhibition and Chemoradiation in Advanced Cervical Cancer (NCT05521997) | Clinical Trial Compass
Not Yet RecruitingPhase 2
Glutaminase Inhibition and Chemoradiation in Advanced Cervical Cancer
United States42 participantsStarted 2026-07-31
Plain-language 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.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Patients eligible for definitive chemoradiotherapy, including brachytherapy
* Patient age ≥ 18 years.
* Patients with histologically confirmed newly diagnosed advanced cervical cancer (squamous, adenosquamous, adenocarcinoma or poorly differentiated); Federation of Gynecology and Obstetrics (FIGO) 2018 clinical stages III-IVA.
* Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
* Absolute neutrophil count ≥ 1,500/mcL.
* Platelets ≥ 100,000/mcL.
* Hemoglobin ≥ 8 g/dL (can be transfused prior to study).
* Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN); patients with known Gilbert disease with serum bilirubin ≤ 3 x ULN may be enrolled.
* Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase \[SGOT\]/alanine aminotransfersase (ALT) (serum glutamate pyruvate transaminase \[SGPT\] ≤ 2.5 x ULN.
* Alkaline phosphatase ≤ 2.5 x ULN.
* Serum creatinine ≤ 1.5 mg/dL to receive weekly cisplatin; patients whose serum creatinine is between 1.5 and 1.9 mg/dL are eligible for cisplatin if there is no hydronephrosis and the estimated creatinine clearance (CCr) is ≥ 30 ml/min. For the purpose of estimating the CCr, formulas, including Cockcroft and Gault for females or similar, should be used.
* International normalize ratio (INR) and activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN (this applies only to patients who do not receive therapeutic anticoagulation; patients receiving therapeutic anticoagulation, such …
What they're measuring
1
Progression-free survival (PFS) - experimental arm only
Timeframe: Through completion of follow-up (estimated to be 24 months and 9 weeks)