A Study Of PF-06647263 In Patients With Advanced Solid Tumors
Stopped early · Phase 1
Conditions studied: Neoplasms, Triple-Negative Breast Cancer
In brief
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.
Key facts
- Study ID
- NCT02078752
- Run by
- Pfizer
- People needed
- 60
- Starts
- 2014-04-09
- Expected to finish
- 2017-05-10
- Last updated by the study team
- 2019-04-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Diagnosis of solid tumor that is advanced/metastatic and resistant to standard therapy or for whom no standard therapy is available
- Performance Status of 0 or 1
- Adequate bone marrow, kidney, and liver function
- Part 2 includes advanced triple negative breast cancer patients.
You may not qualify if…
- Brain metastases requiring steroids
- Major surgery, radiation therapy, or systemic anti-cancer therapy within 4 weeks of study treatment start
- Active and clinically significant bacterial, fungal or viral infection
Where it is running
- Massachusetts General Hospital — Boston, Massachusetts, United States
- Brigham & Women's Hospital (BWH) — Boston, Massachusetts, United States
- Dana-Farber Cancer Institute (DFCI) — Boston, Massachusetts, United States
- Karmanos Cancer Institute — Detroit, Michigan, United States
- Comprehensive Cancer Centers Of Nevada — Las Vegas, Nevada, United States
- Sarah Cannon Research Institute — Nashville, Tennessee, United States
- Tennessee Oncology, PLLC — Nashville, Tennessee, United States
- The University of Texas MD Anderson Cancer Center — Houston, Texas, United States
- Huntsman Cancer Hospital / University of Utah — Salt Lake City, Utah, United States
- Huntsman Cancer Institute-University of Utah — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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