Breast Cancer Clinical Trial

A Study Of PF-06647020 For Adult Patients With Advanced Solid Tumors

Summary

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.

View Eligibility Criteria

Eligibility Criteria

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

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

138

Study ID:

NCT02222922

Recruitment Status:

Completed

Sponsor:

Pfizer

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There are 13 Locations for this study

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University of Alabama at Birmingham
Birmingham Alabama, 35233, United States
University of Alabama at Birmingham
Birmingham Alabama, 35249, United States
Scottsdale Healthcare Hospitals DBA HonorHealth
Scottsdale Arizona, 85258, United States
University of California Davis Comprehensive Cancer Center
Sacramento California, 95817, United States
University of California Davis Medical Center
Sacramento California, 95817, United States
Stanford Cancer Center
Stanford California, 94305, United States
Stanford Hospital and Clinics
Stanford California, 94305, United States
University of Chicago Medicine
Chicago Illinois, 60637, United States
START Midwest
Grand Rapids Michigan, 49503, United States
South Texas Accelerated Research Therapeutics, LLC
San Antonio Texas, 78229, United States
Inova Fairfax Hospital Woodburn GYN Infusion Center
Annandale Virginia, 22003, United States
Mid Atlantic Gynecologic Oncology and Pelvic Surgery Associates (MAGOPSA)
Annandale Virginia, 22003, United States
Fairfax Radiological Consultants
Fairfax Virginia, 22031, United States
Inova Schar Cancer Institute
Fairfax Virginia, 22031, United States
Inova Loudon Hospital
Leesburg Virginia, 20176, United States
Hospital Universitario Fundacion Jimenez Diaz
Madrid , 28040, Spain
Hospital Universitario Madrid Sanchinarro
Madrid , 28050, Spain

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

138

Study ID:

NCT02222922

Recruitment Status:

Completed

Sponsor:


Pfizer

How clear is this clinincal trial information?

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