drugset / Trial / NCT02371369

Phase 3 Study of Pexidartinib for Pigmented Villonodular Synovitis (PVNS) or Giant Cell Tumor of the Tendon Sheath (GCT-TS)

NCT02371369 ↗

Phase 3 Completed 120 enrolled Daiichi Sankyo
RandomizedCrossoverQuadruple-blindTreatment

Summary

This is a Phase 3 clinical study, which aims to evaluate the effectiveness of an investigational drug called pexidartinib for the treatment of certain tumors for which surgical removal could cause more harm than good. The main purpose of this study is to gather information about the investigational drug pexidartinib, which may help to treat tumors of pigmented villonodular synovitis (PVNS) or giant cell tumor of the tendon sheath (GCT-TS). The study consists of two parts with a follow-up period. In Part 1, eligible study participants will be assigned to receive either pexidartinib or matching placebo for 24 weeks. A number of assessments will be carried out during the course of the study, including physical examinations, blood tests, imaging studies, electrocardiograms, and questionnaires. MRI scans will be used to evaluate the response of the tumors to the treatment. Some subjects, assigned to placebo in Part 1 transitioned to pexidartinib for Part 2. Then a protocol amendment was written to allow only pexidartinib patients to continue into Part 2. Part 2 is a long-term treatment phase in which all participants receive open-label pexidartinib. There was also a follow-up period added to Part 2.

Timeline

Start
2015-05-11
Primary completion
2017-03-27
Completion
2021-04-30

Outcome

Met primary endpoint

paper The proportion of patients who achieved overall response was higher for pexidartinib than placebo at week 25 by RECIST PMID 31229240 ↗

paper (24 [39%] of 61 vs none of 59; absolute difference 39% [95% CI 27-53]; p<0·0001). PMID 31229240 ↗

release “the pivotal phase 3 placebo-controlled ENLIVEN (NCT02371369) study of pexidartinib met its primary endpoint of tumor response” daiichisankyo.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Pexidartinib Small molecule 800 mg Oral