Chiauranib for Advanced Solid Tumors and Relapsed/Refractory Small Cell Lung Cancer
This study is testing a drug called Chiauranib for people with advanced solid tumors, including small cell lung cancer (SCLC), that have come back or are resistant to standard treatments. The main goals are to find out how safe Chiauranib is, what side effects it might cause, and to determine the highest dose that can be given safely (MTD) and the recommended dose for future studies (RP2D). You would take Chiauranib once a day in cycles. The study is open to adults aged 18 and older with various advanced solid tumors. This trial is currently recruiting about 36 participants.
- Study design
- This is a Phase 1b/2, single-arm, open-label study, meaning all participants receive Chiauranib and everyone knows what treatment is being given. It aims to enroll about 36 participants.
- What's involved
- Participants will undergo a single-dose period of 6 days, followed by a consecutive-dose period of 28 days. For Phase 2, patients will take Chiauranib once daily for continuous 28-day cycles.
- Compensation
- Not stated in the trial record.
- Follow-up
- Safety will be monitored for up to 30 days after you take your last dose of Chiauranib. Dose-limiting toxicities (DLTs) and the recommended dose will be evaluated over 34 days.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Chiauranib for Advanced Solid Malignant Tumors and Relapsed/Refractory SCLC.
At a glance
Conditions
NCT05271292
Where you'd take part
This study runs at 11 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
California Cancer Associates-Encintas
Encinitas, Californiastudy coordinator listed
Recruiting
Comprehensive Cancer Centers of Nevada
Las Vegas, Nevadastudy coordinator listed
Recruiting
Dana Farber Cancer Institue
Boston, Massachusettsstudy coordinator listed
Recruiting
Gabrail Cancer Center Research
Canton, Ohiostudy coordinator listed
Recruiting
Karmanos Cancer Institute
Detroit, Michiganstudy coordinator listed
Recruiting
North Houston Cancer Clinics
Huntsville, Texasstudy coordinator listed
Recruiting
OU Health
Oklahoma City, Oklahomastudy coordinator listed
Recruiting
Providence/St. Joe Cancer Institute/Crosson Cancer Institute
Fullerton, Californiastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Cabilia Pichardo, MD · STUDY_DIRECTOR · Executive Director of Clinical Development
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Incidence of adverse events (AEs) and other safety parametersUntil 30 days after a patient takes the last dose of the study drug
Number of patients experienced AEs
- Incidence and characteristics of DLTs34 days
Number of patients experienced any dose limited toxicity
- MTD and recommended Phase 2 dose (RP2D)34 days
Determination of recommended phase II dose