CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 6 enrolled
Drug / intervention
PLX3397drug
Likely dose
PLX3397 1000 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02975700
NCT02975700N/ACompleted

A Phase I/II Open Label, Multicenter Study of PLX3397 in Patients With Unresectable or Metastatic KIT-mutated Melanoma

Daiichi Sankyo Co., Ltd.·interventional·Posted Nov 29, 2016·Updated Jan 13, 2026

In Brief

A clinical study evaluating PLX3397 for Melanoma. Completed, enrolled 6 participants across 5 sites in 2 countries.

Detailed Summary

The purpose of this Phase I/II study is to evaluate safety, pharmacokinetics, and preliminary efficacy of the investigational drug PLX3397 in subjects with unresectable or metastatic KIT-mutated melanoma.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMelanoma
CountriesChina, South Korea
CollaboratorsDaiichi Sankyo

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedNov 29, 2016
Enrollment StartJan 31, 2017
Primary CompletionAug 31, 2018
Study CompletionOct 11, 2024
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 9.6 years ago

Interventions

PLX3397drug

1000 mg/day (400 mg in the morning and 600 mg in the evening)