OncoMatch/Clinical Trials/NCT05838521
A Study of Sacituzumab Govitecan (IMMU-132) in Patients With Recurrent or Persistent Cervical Cancer
Is NCT05838521 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Sacituzumab govitecan for cervical cancer.
Treatment: Sacituzumab govitecan — This is a non-randomized Phase 2 study of sacituzumab govitecan (IMMU-132) in subjects with recurrent or persistent cervical cancer.
Check if I qualifyExtracted eligibility criteria
Cancer type
Cervical Cancer
Biomarker criteria
Required: TACSTD2 any tested (testing required; no eligibility threshold specified)
Disease stage
Required: Stage I, II, III, IV
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Must have received: chemotherapy — recurrent or persistent cervical cancer
have progressed following at least one prior chemotherapy treatment regimen
Cannot have received: topoisomerase I inhibitor
Have previously received topoisomerase I inhibitors
Cannot have received: irinotecan (irinotecan)
Exception: history of anaphylactic reaction or ≥ Grade 3 toxicity
history of an anaphylactic reaction to irinotecan or ≥ Grade 3 toxicity to prior irinotecan
Lab requirements
Blood counts
WBC ≥ 3,000/ul, Platelets ≥ 75,000/ul, Granulocytes ≥ 1500/ul
Kidney function
creatinine ≤ 2.0 mg/dL
Liver function
bilirubin ≤ 1.5 institutional upper limit of normal, AST and ALT ≤ 2.5 × IULN or ≤ 5 × IULN if known liver metastases
adequate bone marrow function: WBC ≥ 3,000/ul, Platelets ≥ 75,000/ul, Granulocytes ≥ 1500/ul. adequate renal function: creatinine ≤ 2.0 mg/dL. adequate hepatic function: bilirubin ≤ 1.5 institutional upper limit of normal, AST and ALT ≤ 2.5 × IULN or ≤ 5 × IULN if known liver metastases
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Smilow Cancer Hospital at Yale New Haven · New Haven, Connecticut
- Cleveland Clinic · Cleveland, Ohio
Showing up to 5 US sites. See all sites on ClinicalTrials.gov →
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