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OncoMatch/Clinical Trials/NCT05271292

Chiauranib for Advanced Solid Malignant Tumors and Relapsed/Refractory SCLC.

Is NCT05271292 recruiting? Yes, currently enrolling (May 2026). This Phase 1/2 trial studies Chiauranib for small cell lung cancer.

Phase 1/2RecruitingChipscreen Biosciences, Ltd.NCT05271292Data as of May 2026

Treatment: ChiauranibThis is a Phase 1b/2, single-arm, open-label, dose-escalation study including 2 stages: Phase 1b: Dose-Escalation Stage (Single-Dose and Consecutive-Dose Periods) Phase 2: recommended Phase 2 dose (RP2D) of chiauranib will be given to all patients enrolled in this phase once daily for 28-day cycles continuously with no interruption between cycles.

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Extracted eligibility criteria

Cancer type

Small Cell Lung Cancer

Tumor Agnostic

Disease stage

Metastatic disease required

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Must have received: standard therapy — relapsed/refractory or no standard therapy exists

relapsed from or is refractory to standard therapy or for which no standard therapy exists

Cannot have received: systemic anticancer therapy

Exception: must be >21 days before enrollment

Patient has received any systemic anticancer therapy (including chemotherapy, targeted therapy, biological immunotherapy, any investigational drug, or anti-cancer herbal medicine) within 21 days before enrollment

Cannot have received: blood support therapy (blood transfusion, blood products, hematopoiesis stimulating agents such as granulocyte-colony stimulating factor [G-CSF])

Exception: must be >2 weeks before enrollment

any blood support therapy (including blood transfusion, blood products, or hematopoiesis stimulating agents such as granulocyte-colony stimulating factor [G-CSF]) within 2 weeks before enrollment

Cannot have received: systemic corticosteroids

Exception: dose >10 mg prednisone or equivalent

Patients who are receiving corticosteroids at a dose of > 10 mg prednisone or equivalent of other systemic steroids will be excluded

Cannot have received: Aurora kinase inhibitor

Exception: toxicity leading to discontinuation

Patient has previously experienced toxicity leading to discontinuation of treatment with Aurora kinase inhibitors

Cannot have received: VEGF/VEGFR inhibitor (sorafenib, sunitinib, pazopanib, bevacizumab, regorafenib, axitinib, vandetanib, dasatinib)

Exception: toxicity leading to discontinuation

Patient has previously experienced toxicity leading to discontinuation of treatment with ... VEGF/VEGFR inhibitors, such as sorafenib, sunitinib, pazopanib, bevacizumab, regorafenib, axitinib, vandetanib, or dasatinib

Lab requirements

Blood counts

ANC ≥1.5×10^9/L, platelet ≥100×10^9/L, hemoglobin ≥100 g/L

Kidney function

creatinine clearance >60 mL/min (Cockcroft-Gault equation)

Liver function

total bilirubin ≤1.25×ULN, ALT and AST ≤1.5×ULN (≤5×ULN for patients with hepatic metastasis)

Cardiac function

NYHA grade II or higher congestive cardiac failure, unstable angina, MI within 6 months, significant arrhythmia, LVEF <50%, primary cardiomyopathies, prolonged QTc, QTcF >470ms (female) or >450ms (male), coronary heart disease with symptoms requiring medication

Major organ functions meet the following criteria ... Hematology: ANC ≥1.5×10^9/L, platelet ≥100×10^9/L, hemoglobin ≥100 g/L. Biochemistry: total bilirubin ≤1.25×ULN, ALT and AST ≤1.5×ULN (≤5×ULN for patients with hepatic metastasis), creatinine clearance >60 mL/min (Cockcroft-Gault equation), fasting triglyceride ≤3.0 mmol/L, fasting total cholesterol ≤7.75 mmol/L. Coagulation panel: INR <1.5.

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

US trial sites

  • California Cancer Associates-Encintas · Encinitas, California
  • Providence/St. Joe Cancer Institute/Crosson Cancer Institute · Fullerton, California
  • Winship Cancer Institute of Emory University · Atlanta, Georgia
  • Dana Farber Cancer Institue · Boston, Massachusetts
  • Karmanos Cancer Institute · Detroit, Michigan

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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