drugset / Trial / NCT07379047

Efficacy and Safety of NB003 in Patients With Advanced Gastrointestinal Stromal Tumors (GIST)

NCT07379047

Phase 2/3 Recruiting 255 enrolled Ningbo Newbay Technology Development Co., Ltd
RandomizedCrossoverOpen-labelTreatment

Summary

NB003-04 is a phase II/III, multicenter, open-label clinical study designed to evaluate the efficacy, safety, and pharmacokinetic (PK) profile of NB003 in patients with gastrointestinal stromal tumors aged 18 years and above (or the legal adult age of consent per local regulations, whichever is older). Participants who are eligible for this study are those who have experienced disease progression or documented intolerance following treatment with either imatinib and sunitinib or following treatment with imatinib. This study consists of two parts. Part 1 (hereinafter referred to as Part 1) compares the efficacy of NB003 versus regorafenib in patients who need a third-line therapy for GIST who have failed sequential therapy with imatinib and sunitinib. Part 2 (hereinafter referred to as Part 2) evaluates the efficacy of NB003 in patients who need a second-line therapy for GIST who have failed treatment with imatinib.

Timeline

Start
2026-05-11
Primary completion
2028-08-01
Completion
2028-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject NB003 Unknown 15 mg
Comparator Regorafenib Small molecule 160 mg Oral