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.

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NCT05271292

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

UNKNOWN
PHASE1Ages 18+InterventionalTreatment
Chipscreen Biosciences, Ltd.
~36 participants
Updated 2024-07-16 on ClinicalTrials.gov
What's tested:Chiauranib

At a glance

Recruiting sites
11 of 11 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Incidence of adverse events (AEs) and other safety parameters
Measured over Until 30 days after a patient takes the last dose of the study drug
+2 more outcomes measured
Small Cell Lung Cancer
Advanced Solid Malignant Tumor

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.

  • Cabilia Pichardo, MD · STUDY_DIRECTOR · Executive Director of Clinical Development

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  • 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