drugset / Trial / NCT02078752
A Study Of PF-06647263 In Patients With Advanced Solid Tumors
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PF-06647263 | Unknown | 0.015 mg/kg | Intravenous |