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OncoMatch/Clinical Trials/NCT05271292

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

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

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

Treatments studied

Targeted therapy

Chiauranib

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 →

Frequently asked questions

Is NCT05271292 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior systemic anticancer therapy, blood support therapy, systemic corticosteroids disqualifies patients from enrollment.

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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