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Terminated Phase 1Phase 2 Interventional Results available

A Study of PF-06873600 in People With Cancer

ClinicalTrials.gov ID: NCT03519178

Public ClinicalTrials.gov record NCT03519178. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 5:33 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

PHASE 1/2A DOSE ESCALATION AND EXPANSION STUDY EVALUATING SAFETY, TOLERABILITY, PHARMACOKINETIC, PHARMACODYNAMICS AND ANTI-TUMOR ACTIVITY OF PF-06873600 AS A SINGLE AGENT AND IN COMBINATION WITH ENDOCRINE THERAPY

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this clinical trial is to learn about the safety and effects of study medicine (PF-06873600) when taken alone or with hormone therapy by people with cancer. People may be able to participate in this study if they have the following types of cancer: Hormone Receptor positive (HR+) breast cancer; Human Epidermal Growth Factor Receptor 2 (HER2)-negative breast cancer that is advanced or metastatic (spread to other parts of the body); triple negative breast cancer; epithelial ovarian cancer; fallopian tube cancer; or primary peritoneal cancer. All participants in this study will receive the study medicine by mouth, 1 to 2 times a day at home. The dose of the study medicine may be changed during the study. Some participants will also receive hormone therapy. The hormone therapy will be either letrozole by mouth once a day at home, or fulvestrant as a shot into the muscle. Fulvestrant will be given every two weeks at the study clinic for the first month, and then once a month after that. Participants will take part in this study for at least 7 to 8 months, depending on how they respond to the therapy. During this time participants will visit the study clinic once a week for the first 2 cycles and every cycle thereafter.

Study identification

NCT ID
NCT03519178
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
155 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 7, 2018 (Actual)
Primary completion
Apr 5, 2023 (Actual)
Completion
Oct 30, 2024 (Actual)
Last update posted
Nov 14, 2025

2018 – 2024

United States locations

U.S. sites
39
U.S. states
11
U.S. cities
25
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35233 —
University Of Alabama at Birmingham Birmingham Alabama 35249 —
HonorHealth Scottsdale Arizona 85258 —
Virginia G. Piper Cancer Center Pharmacy Scottsdale Arizona 85258 —
Highlands Oncology Group Fayetteville Arkansas 72703 —
Highlands Oncology Group Rogers Arkansas 72758 —
Highlands Oncology Group Springdale Arkansas 72762 —
Highlands Oncology Springdale Arkansas 72762 —
The Oncology Institute of Hope and Innovation Glendale California 91204 —
The Oncology Institute of Hope and Innovation Long Beach California 90805 —
UCSF Helen Diller Family Comprehensive Cancer Center San Francisco California 94143 —
UCSF Investigational Drugs Pharmacy San Francisco California 94158 —
The Oncology Institute of Hope and Innovation Santa Ana California 92705 —
UCLA Hematology/Oncology - Parkside Santa Monica California 90404 —
UCLA Hematology/Oncology - Santa Monica Santa Monica California 90404 —
The Oncology Institute of Hope and Innovation Whittier California 90602 —
University of Colorado Hospital - Anschutz Cancer Pavilion (ACP) Aurora Colorado 80045 —
University of Colorado Hospital - Anschutz Inpatient Pavilion (AIP) Aurora Colorado 80045 —
University of Colorado Hospital - Anschutz Outpatient Pavilion (AOP) Aurora Colorado 80045 —
UCHealth Lone Tree Medical Center Lone Tree Colorado 80124 —
Holy Cross Hospital Fort Lauderdale Florida 33308 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Brigham & Women's Hospital Boston Massachusetts 02115 —
Dana Farber Cancer Institute Boston Massachusetts 02215 —
Dana-Farber Cancer Institute Boston Massachusetts 02215 —
Memorial Sloan Kettering Cancer Center Long Island City New York 11101 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
Tennessee Oncology, PLLC Nashville Tennessee 37203 —
The Sarah Cannon Research Institute-Pharmacy Nashville Tennessee 37203 —
The Sarah Cannon Research Institute Nashville Tennessee 37203 —
The University of Texas MD Anderson Cancer Center Houston Texas 77030 —
South Texas Accelerated Research Therapeutics, LLC San Antonio Texas 78229 —
Northwest Medical Specialties, PLLC Federal Way Washington 98003 —
Northwest Medical Specialties, PLLC Gig Harbor Washington 98332 —
Rainier Hematology-Oncology PC Puyallup Washington 98373 —
Rainier Hematology-Oncology, PC Puyallup Washington 98373 —
Fred Hutchinson Cancer Center Seattle Washington 98109 —
University of Washington Medical Center Seattle Washington 98195 —
Northwest Medical Specialties, PLLC Tacoma Washington 98405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03519178, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 14, 2025 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03519178 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →