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.
Treatment: Chiauranib — This 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.
Check if I qualifyExtracted eligibility criteria
Treatments studied
Targeted therapy
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.
Check if I qualifyRelated pages