Skip to main content
TrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor about whether a trial is right for you.
RECRUITINGPhase 1INTERVENTIONAL

A Study to Learn About the Study Medicine Called PF-08046876 in People With Advanced Solid Tumors

A Phase 1 Open-label Study to Investigate PF-08046876 in Adult Participants With Advanced Solid Tumors.

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The purpose of the study is to explore the safety and effects of the study drug (PF-08046876) in people diagnosed with advanced cancer of the bladder, lung, head and neck, esophagus, or pancreas. PF-08046876 is an investigational anticancer therapy called an 'antibody drug conjugate' or 'ADC'. ADCs are anticancer drugs designed to stick to cancer cells and kill them. The study drug will be given to participants through a needle in a vein (intravenous infusion). This study includes multiple parts. In the first part of the study, there will be different groups of people receiving different doses of the study drug. The study may also test different schedules.

Who May Be Eligible (Plain English)

Who May Qualify: - 18 years of age or older - Advanced cancer of the bladder, lung, head and neck, esophagus, or pancreas - Measurable disease - You should be able to carry out daily activities with 0 level of ability (ECOG 0)-1 - Part 1: progression or relapse following standard treatments - Part 2: maximum of 2 prior lines of systemic therapy in the advanced setting - Resolution of acute effects of prior anticancer therapy to baseline or Grade 1 - Consent to submit required pre-treatment tumor tissue as medically feasible Who Should NOT Join This Trial: - Received prior treatment with an antibody drug conjugate with a camptothecin-class payload (e.g. sacituzumab govitecan, trastuzumab deruxtecan ) - Active anorexia, nausea or vomiting, and/or signs of intestinal obstruction meeting protocol exclusion - Pulmonary disease meeting protocol exclusion - Other unacceptable abnormalities as defined by protocol Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * 18 years of age or older * Advanced cancer of the bladder, lung, head and neck, esophagus, or pancreas * Measurable disease * ECOG Performance status 0-1 * Part 1: progression or relapse following standard treatments * Part 2: maximum of 2 prior lines of systemic therapy in the advanced setting * Resolution of acute effects of prior anticancer therapy to baseline or Grade 1 * Consent to submit required pre-treatment tumor tissue as medically feasible Exclusion criteria: * Received prior treatment with an antibody drug conjugate with a camptothecin-class payload (e.g. sacituzumab govitecan, trastuzumab deruxtecan ) * Active anorexia, nausea or vomiting, and/or signs of intestinal obstruction meeting protocol exclusion * Pulmonary disease meeting protocol exclusion * Other unacceptable abnormalities as defined by protocol

Treatments Being Tested

DRUG

PF-08046876

Intravenous administration

Locations (20)

City of Hope National Medical Center
Duarte, California, United States
City of Hope at Irvine Lennar
Irvine, California, United States
Ronald Reagan UCLA Medical Center
Los Angeles, California, United States
UCLA Department of Medicine-Hematology/Oncology
Los Angeles, California, United States
Santa Monica UCLA Medical Center & Orthopaedic Hospital
Santa Monica, California, United States
UCLA Hematology/Oncology - Santa Monica
Santa Monica, California, United States
Smilow Cancer Hospital - Yale New Haven Health
New Haven, Connecticut, United States
Yale - New Haven Hospital - Yale Cancer Center
New Haven, Connecticut, United States
Smilow Cancer Hospital Phase 1 Unit
New Haven, Connecticut, United States
Smilow Cancer Hospital - Trumbull
Trumbull, Connecticut, United States
Brigham and Women's Hospital
Boston, Massachusetts, United States
Dana-Farber Cancer Institute
Boston, Massachusetts, United States
Dana-Farber Cancer Institute - Chestnut Hill
Newton, Massachusetts, United States
Sarah Cannon Research Institute - Pharmacy
Nashville, Tennessee, United States
SCRI Oncology Partners
Nashville, Tennessee, United States
The University of Texas MD Anderson Cancer Center - Conroe
Conroe, Texas, United States
University of Texas MD Anderson Cancer Center
Houston, Texas, United States
The University of Texas, MD Anderson Cancer Center - West Houston
Houston, Texas, United States
The University of Texas, MD Anderson Cancer Center - League City
League City, Texas, United States
NEXT Oncology
San Antonio, Texas, United States