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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 (Jun 2026). This Phase 2 trial studies Sacituzumab govitecan for cervical cancer.

Phase 2RecruitingYale UniversityNCT05838521Data as of Jun 2026

Treatment: Sacituzumab govitecanThis is a non-randomized Phase 2 study of sacituzumab govitecan (IMMU-132) in subjects with recurrent or persistent cervical cancer.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Sacituzumab govitecan

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)

Demographics

Female only

Prior therapy

Max 2 prior lines
Min 1 prior line

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 →

Frequently asked questions

Is NCT05838521 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior topoisomerase I inhibitor, irinotecan disqualifies patients from enrollment.

Does this trial require TACSTD2?

Yes, TACSTD2 any tested is a required biomarker for enrollment.

What disease stage is eligible?

Stage I or II or III or IV is required.

Is this trial open to male patients?

No. This trial enrolls female patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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