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Clinical Trial Summary

The objective of this observational study is to explore the efficacy and safety of ripretinib treatment combined with surgery in advanced gastrointestinal stromal tumors(GIST) after failure of imatinib therapy.


Clinical Trial Description

This study is a single-arm, multicenter, observational study. A total of approximately 30 subjects were be enrolled. The patient was orally administered with ripretinib150 mg QD. 4 weeks for one cycle. Efficacy was assessed every two cycles. For subjects with PR or SD after ripretinib treatment, resection of gastrointestinal stromal tumor was performed after discussion by MDT and ensure R0 resection as much as possible.Ripretinib 150mg QD was continued 2 weeks after surgery. Thereafter, subjectss entered the follow-up period for at least 1 year. Safety and survival information will be collected ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05354388
Study type Observational
Source Sichuan Provincial People's Hospital
Contact Minghui Pang, Professor
Phone 18981838525
Email pangmh2000@163.com
Status Recruiting
Phase
Start date October 1, 2021
Completion date December 30, 2023

See also
  Status Clinical Trial Phase
Completed NCT04633122 - A Study to Assess the Efficacy and Safety of DCC-2618 and Sunitinib in Patients With Advanced Gastrointestinal Stromal Tumors After Treatment With Imatinib Phase 2
Completed NCT03440515 - Management of Imatinib-associated Severe Skin Rash in Patients With Gastrointestinal Stromal Tumor Phase 2