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Spots Global Cancer Trial Database for Study Of OX40 Agonist PF-04518600 Alone And In Combination With 4-1BB Agonist PF-05082566

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Trial Identification

Brief Title: Study Of OX40 Agonist PF-04518600 Alone And In Combination With 4-1BB Agonist PF-05082566

Official Title: A PHASE 1, OPEN-LABEL, DOSE ESCALATION STUDY OF PF-04518600 AS A SINGLE AGENT AND IN COMBINATION WITH PF-05082566 IN PATIENTS WITH SELECTED LOCALLY ADVANCED OR METASTATIC CANCERS

Study ID: NCT02315066

Conditions

Neoplasms

Study Description

Brief Summary: To assess the safety and tolerability at increasing dose levels of PF-04518600 alone or in combination wtih PF-05082566 in patients with select advanced or metastatic carcinoma in order to determine the maximum tolerated dose and select the recommended Phase 2 dose.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

The Angeles Clinic And Research Institute, A Cedars-Sinai Affiliate, Los Angeles, California, United States

Keck Hospital of USC, Los Angeles, California, United States

LAC+USC Medical Center, Los Angeles, California, United States

USC/Norris Comprehensive Cancer Center, Los Angeles, California, United States

Ronald Regan Medical Center, Los Angeles, California, United States

UCLA Hematology & Oncology Clinic, Los Angeles, California, United States

Hoag Memorial Hospital Presbyterian, Newport Beach, California, United States

Medical Imaging Center of Southern California, Inc., Santa Monica, California, United States

Santa Monica UCLA Hematology & Oncology Clinic, Santa Monica, California, United States

UConn Health, Pharmacy, Farmington, Connecticut, United States

UConn Health, Neag Comprehensive Cancer Center, Farmington, Connecticut, United States

H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, United States

Massachusetts General Hospital (MGH), Boston, Massachusetts, United States

Brigham & Women's Hospital (BWH), Boston, Massachusetts, United States

Beth Israel Deaconess Medical Center (BIDMC), Boston, Massachusetts, United States

Dana-Farber Cancer Institute (DFCI), Boston, Massachusetts, United States

Massachusetts General/Chelsea HealthCare Center, Chelsea, Massachusetts, United States

Mass General/North Shore Center for Outpatient Care, Danvers, Massachusetts, United States

Mass General West, Waltham, Massachusetts, United States

Columbia University Medical Center - Herbert Irving Pavilion, New York, New York, United States

Methodist Hospital-Pathology, Houston, Texas, United States

The University of Texas MD Anderson Cancer Center, Houston, Texas, United States

Seattle Cancer Care Alliance, Seattle, Washington, United States

University of Washington Medical Center, Seattle, Washington, United States

Groupe hospitalier Pitie Salpetriere, Paris, , France

Institut Gustave Roussy, Villejuif, , France

National Cancer Center Hospital East, Kashiwa, Chiba, Japan

The Netherlands Cancer Institute, Amsterdam, , Netherlands

Slotervaart Hospital/Antoni van Leeuwenhoek, Amsterdam, , Netherlands

Erasmus MC, Rotterdam, , Netherlands

Contact Details

Name: Pfizer CT.gov Call Center

Affiliation: Pfizer

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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