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Recruiting NCT05464875

NCT05464875 A Multicenter Study of Avapritinib Efficacy and Safety of Metastatic or Unresectable Gastrointestinal Stromal Tumors

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Clinical Trial Summary
NCT ID NCT05464875
Status Recruiting
Phase
Sponsor Xinhua Zhang, MD
Condition Gastrointestinal Stromal Tumors
Study Type OBSERVATIONAL
Enrollment 74 participants
Start Date 2022-07-09
Primary Completion 2025-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 74 participants in total. It began in 2022-07-09 with a primary completion date of 2025-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This is a prospective, multicenter, observational real-world study to explore the therapy patterns and clinical outcomes of Avapritinib in patients with metastatic or unresectable gastrointestinal stromal tumors.

Eligibility Criteria

Inclusion Criteria: * Patients who are aged ≥ 18 years. * Gastrointestinal stromal tumors confirmed by histopathological examination, and CD- and/or DOG-1-positive by immunohistochemistry. * Presence of mRECIST v1.1-compliant lesions with at least one measurable lesion (non-lymphadenopathy ≥1.0 cm or ≥2-fold scan slice thickness). * Treatment with Avapritinib. * Patients with an Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 to 2 at screening. * Patient informed consent and signed written consent form. * The patient was compliant and voluntarily scheduled for follow-up, treatment, laboratory tests, and other study procedures. Exclusion Criteria: * KIT or PDGFRA wild type. * Failure to complete continuous atorvastatin for at least 15 days due to intolerability or disease progression. * Other serious acute or chronic physical or mental problems, or laboratory abnormalities, may increase the risk associated with participation in the study or use of drugs, or interfere with the judgment of the study results and, in the judgment of the investigator, are not considered appropriate for participation in the investigator.

Contact & Investigator

Central Contact

Xinhua Zhang, PhD

✉ zhangxinhua@mail.sysu.edu.cn

📞 +8620-87332200

Principal Investigator

Xinhua Zhang, PhD

PRINCIPAL INVESTIGATOR

First affiliated hosptial,Sun Yat-sen university

Frequently Asked Questions

Who can join the NCT05464875 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Gastrointestinal Stromal Tumors. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05464875 currently recruiting?

Yes, NCT05464875 is actively recruiting participants. Contact the research team at zhangxinhua@mail.sysu.edu.cn for enrollment information.

Where is the NCT05464875 trial being conducted?

This trial is being conducted at Guangzhou, China.

Who is sponsoring the NCT05464875 clinical trial?

NCT05464875 is sponsored by Xinhua Zhang, MD. The principal investigator is Xinhua Zhang, PhD at First affiliated hosptial,Sun Yat-sen university. The trial plans to enroll 74 participants.

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