drugset / Trial / NCT01804530

Phase 1 Study of PLX7486 as Single Agent in Patients With Advanced Solid Tumors

NCT01804530 ↗

Phase 1 Terminated 59 enrolled Plexxikon
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to determine the safety, pharmacokinetics, maximum tolerated dose/recommended Phase 2 dose, and efficacy of PLX7486.

Timeline

Start
2013-08
Primary completion
2018-01-24
Completion
2018-01-24

Outcome

Outcome not reported

Stopped: “Discontinued”

Drugs

EvaluationDrugModalityDoseRoute
Subject PLX7486 Unknown 50 mg —