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OncoMatch/Clinical Trials/NCT03872661

Neoadjuvant IBI308, Bevacizumab, Plus Pemetrexed and Carboplatin Followed by Surgery in Unresectable Stage III NSCLC

Is NCT03872661 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including IBI308 and Bevacizumab for lung cancer stage iii.

Phase 2RecruitingSun Yat-sen UniversityNCT03872661Data as of Jun 2026Location: China

Treatment: IBI308 · Bevacizumab · Pemetrexed · CarboplatinThe purpose of this study is to studying neoadjuvant IBI308, bevacizumab, plus pemetrexed and carboplatin followed by surgery to see how well it works in treating patients with unresectable stage III non-small cell lung cancer.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Bevacizumab

Chemotherapy

PemetrexedCarboplatin

Other

IBI308

Cancer type

Non-Small Cell Lung Carcinoma

Small Cell Lung Cancer

Biomarker criteria

Required: ALK wild-type

Required: EGFR wild-type

Disease stage

Required: Stage III

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: anti-pd-1/pd-l1/pd-l2 or anti-ctla-4 antibody

Cannot have received: chemotherapy

Cannot have received: radiotherapy

Lab requirements

Blood counts

ANC ≥2.0 x 10^9/L, Platelet count ≥100 x 10^9/L, Hemoglobin ≥9 g/dL (may be transfused to maintain or exceed this level)

Kidney function

Serum creatinine ≤ 1.25 x ULN, or ≥ 60 ml/min

Liver function

Total bilirubin ≤ 1.5 x ULN; AST, ALT ≤ 2.5 x ULN in subjects without liver metastases; ≤ 5 x ULN in subjects with liver metastases

Adequate hematological function: Absolute neutrophil count (ANC) ≥2.0 x 109/L, and Platelet count ≥100 x 109/L, and Hemoglobin ≥9 g/dL (may be transfused to maintain or exceed this level). Adequate liver function: Total bilirubin ≤ 1.5 x upper limit of normal (ULN), Aspartate aminotransferase (AST), alanine aminotransferase (ALT) ≤ 2.5 x ULN in subjects without liver metastases; ≤ 5 x ULN in subjects with liver metastases. Adequate renal function: Serum creatinine ≤ 1.25 x ULN, or ≥ 60 ml/min.

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

Frequently asked questions

Is NCT03872661 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Does this trial require ALK?

Yes, ALK wild-type is a required biomarker for enrollment.

Does this trial require EGFR?

Yes, EGFR wild-type is a required biomarker for enrollment.

What disease stage is eligible?

Stage III is required.

Is there an age limit?

Yes. Patients must be 75 years or younger.

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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