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OncoMatch/Clinical Trials/NCT06540729

RC48 in Combination With AK104 and Bevacizumab in OCCC

Is NCT06540729 recruiting? Yes, currently enrolling (Sep 2026). This Phase 2 trial studies Disitamab vedotin in combination with AK104 and bevacizumab for the treatment of recurrent and persistent clear cell ovarian cancer for ovary cancer.

Phase 2RecruitingSun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityNCT06540729Data as of Sep 2026Location: China

Treatment: Disitamab vedotin in combination with AK104 and bevacizumab for the treatment of recurrent and persistent clear cell ovarian cancerDisitamab vedotin (RC48) in combination with AK104 (PD-1/CTLA-4 bispecific) and bevacizumab for the treatment of recurrent and persistent clear cell ovarian cancer: a single-arm, phase II, multicenter study (DAB OCC study)

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Disitamab vedotin in combination with AK104 and bevacizumab for the treatment of recurrent and persistent clear cell ovarian cancer

Cancer type

Ovarian Cancer

Biomarker criteria

Required: HER2 (ERBB2) ihc ≥1+ (ihc ≥1+)

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75
Female only

Prior therapy

Max 2 prior lines

Lab requirements

Blood counts

white blood cell count ≥3.0×10^9/l, neutrophil count ≥1.5×10^9/l, platelet count ≥100×10^9/l, hemoglobin ≥80 g/l

Kidney function

creatinine ≤1.5× uln

Liver function

ast ≤2.5× uln, alt ≤2.5× uln, serum total bilirubin ≤1.5× uln

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT06540729 currently recruiting?

Yes, this trial is currently recruiting patients.

Does this trial require ERBB2?

Yes, ERBB2 ihc ≥1+ is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 75 years or younger.

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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