drugset / Trial / NCT02078752

A Study Of PF-06647263 In Patients With Advanced Solid Tumors

NCT02078752 ↗

Phase 1 Terminated 60 enrolled Pfizer
NaSingle-groupOpen-labelTreatment

Summary

To assess the safety and tolerability at increasing dose levels of PF-06647263 in patients with advanced solid tumors in order to determine the maximum tolerated dose and select the recommended Phase 2 dose.

Timeline

Start
2014-04-09
Primary completion
2017-05-10
Completion
2017-05-10

Outcome

Outcome not reported

Stopped: “The study was terminated due to a change in sponsor prioritization.”

Drugs

EvaluationDrugModalityDoseRoute
Subject PF-06647263 Unknown 0.015 mg/kg Intravenous