120
Participants
Start Date
June 1, 2022
Primary Completion Date
May 31, 2029
Study Completion Date
November 30, 2029
Pembrolizumab
Treatment at 200 mg pembrolizumab, administered intravenously (IV) on Day 1 of each 21-day cycle prior to infusion of FF-10832
FF-10832
Following administration of pembrolizumab, FF-10832 Gemcitabine Liposome Injection, 40 mg/m2 administered intravenously (IV) on Day 1 of each 21-day cycle
NYU Langone Health, New York
Icahn School of Medicine at Mount Sinai, New York
UPMC Hillman Cancer Center, Pittsburgh
Hospital of the Univ of Pennsylvania Perlman Center, Philadelphia
Sibley Memorial Hospital, Washington D.C.
Virginia Cancer Specialists, PC, Fairfax
Medical University of South Carolina, Charleston
Sarah Cannon Research Institute, Nashville
University of Louisville Brown Cancer Center, Louisville
University of Kentucky Medical Center, Lexington
TriHealth Cancer Institute; Good Samaritan Hospital, Cincinnati
Henry Ford Cancer - Detroit (Brigitte Harris Cancer Pavilion), Detroit
University of Wisconsin Clinical Science Center, Madison
Avera Cancer Institute, Sioux Falls
Washington University School of Medicine, Center for Adv Medicine, St Louis
University of Kansas Cancer Center - Westwood, Westwood
Nebraska Cancer Specialists - Legacy, Omaha
University of Texas Southwestern Medical Center, Dallas
Comprehensive Cancer Centers of Nevada - Southern Hills, Las Vegas
Cancer and Blood Speciality Clinic, Long Beach
Sharp Memorial Hospital (Oncology Clinical Research), San Diego
Providence Cancer Institute Franz Clinic, Portland
Atlantic Health System / Morristown Medical Center, Morristown
Lead Sponsor
Merck Sharp & Dohme LLC
INDUSTRY
Fujifilm Pharmaceuticals U.S.A., Inc.
INDUSTRY