OncoMatch

OncoMatch/Clinical Trials/NCT06769971

Phase II Study of Ivonescimab and Cadonilimab in Combination with Chemotherapy in Patients with ES-SCLC

Is NCT06769971 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Ivonescimab and Cadonilimab for small cell lung cancer.

Phase 2RecruitingSichuan UniversityNCT06769971Data as of May 2026

Treatment: Ivonescimab · Cadonilimab · Etoposide · CarboplatinThis is a phase II study. All patients are treatment naive extensive stage small cell lung cancer(ES-SCLC), Eastern Cooperative Oncology Group (ECOG) performance status 0-1. The purpose of this study is to evaluate the efficacy and safety of Ivonescimab and Cadonilimab in combination with chemotherapy in patients with ES-SCLC.

Check if I qualify

Extracted eligibility criteria

Cancer type

Small Cell Lung Cancer

Disease stage

Required: Stage IV

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Max 0 prior lines

Cannot have received: systemic therapy

Exception: ES-SCLC patients who had received definitive chemoradiotherapy for limited-stage small-cell lung cancer but had disease progression > 6 months earlier

Had not received previous systemic therapy; Or ES-SCLC patients who had received definitive chemoradiotherapy for limited-stage small-cell lung cancer but had disease progression > 6 months earlier

Cannot have received: immunotherapy targeting tumor immunity

Subjects who received any prior treatments targeting the mechanism of tumor immunity

Cannot have received: anti-angiogenic therapy

Subjects who received any prior anti-angiogenic therapy

Cannot have received: palliative local treatment

Received palliative local treatment within 2 weeks prior to the first dose

Cannot have received: non-specific immunomodulatory treatment

non-specific immunomodulatory treatment within 2 weeks prior to the first dose

Cannot have received: Chinese herbal medicine or traditional Chinese medicinal products with anti-tumor indications

Chinese herbal medicine or traditional Chinese medicinal products with anti-tumor indications within 1 weeks prior to the first dose

Lab requirements

Blood counts

Kidney function

Liver function

Have adequate organ function

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

Could you qualify for this trial?

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

Check if I qualify