A Study Of PF-06647020 For Adult Patients With Advanced Solid Tumors
To assess the safety and tolerability at increasing dose levels of PF-06647020 in patients with advanced solid tumors in order to determine the maximum tolerated dose and select the recommended Phase 2 dose.
Checked against the public recordLast updated Dec 17, 2020 · Source: ClinicalTrials.gov
What this study is about
- Purpose
- Treatment
- Study type
- Interventional
- Phase
- Phase 1
- Sponsor
- Pfizer
- Interventions being studied
- Drug: PF-06647020 Q3W; Drug: fluconazole; Drug: PF-06647020 Q2W; Drug: PF-06647020 combined with Avelumab
How this study is categorized
These labels come from structured fields and exact terms in the public record.
Who may be able to participate
Q2W Inclusion Criteria: * Diagnosis of platinum resistant or refractory OVCA having received 2 or fewer prior lines, or recurrent advanced NSCLC having received 3 or fewer prior lines * Performance Status of 0, 1, or 2 * Adequate bone marrow, kidney, and liver function Q2W Exclusion Criteria: * OVCA pts excluded with any of the following: non-epithelial, including malignant mixed mullerian tumors, unresolved bowel obstruction * 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 Q3W Inclusion Criteria: * 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 ovarian cancer, target expressing triple negative breast cancer and non small cell lung cancer patients Q3W Exclusion Criteria: * OVCA pts excluded with any of the following: non-epithelial, including malignant mixed mullerian tumors, prior radiotherapy to pelvis/abdomen, pts with CA-125 only disease, unresolved bowel obstruction * 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
Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.
U.S. locations
- University of Alabama at BirminghamBirmingham, Alabama
- University of Alabama at BirminghamBirmingham, Alabama
- Scottsdale Healthcare Hospitals DBA HonorHealthScottsdale, Arizona
- University of California Davis Comprehensive Cancer CenterSacramento, California
- University of California Davis Medical CenterSacramento, California
- Stanford Cancer CenterStanford, California
- Stanford Hospital and ClinicsStanford, California
- University of Chicago MedicineChicago, Illinois
- START MidwestGrand Rapids, Michigan
- South Texas Accelerated Research Therapeutics, LLCSan Antonio, Texas
- Inova Fairfax Hospital Woodburn GYN Infusion CenterAnnandale, Virginia
- Mid Atlantic Gynecologic Oncology and Pelvic Surgery Associates (MAGOPSA)Annandale, Virginia
Source and freshness
Processed from ClinicalTrials.gov. Last public update: Dec 17, 2020. Always confirm current availability with the study team.