174
Participants
Start Date
October 17, 2018
Primary Completion Date
January 16, 2026
Study Completion Date
January 16, 2026
pembrolizumab
Administered as an IV infusion every 3 weeks (Q3W)
Favezelimab
Administered as an IV infusion Q3W
Concord Repatriation & General Hospital ( Site 0203), Concord
St Vincent s Hospital (Melbourne) Limited ( Site 0202), Fitzroy
Monash Health ( Site 0201), Clayton
Princess Alexandra Hospital ( Site 0204), Woollongabba
Universitaetsklinikum Leipzig AOeR ( Site 0327), Leipzig
Fox Chase Cancer Center ( Site 0019), Philadelphia
Humanitas-U.O di Oncologia medica ed Ematologia ( Site 0352), Rozzano
A.O. Universitaria Policlinico S. Orsola-Malpighi ( Site 0351), Bologna
Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori ( Site 0354), Meldola
U. klinikum Koeln AOER ( Site 0326), Cologne
Texas Oncology-Austin Midtown ( Site 8002), Austin
Banner MD Anderson Cancer Center ( Site 0020), Gilbert
Ronald Reagan UCLA Medical Center (Radiological Sciences) ( Site 0007), Los Angeles
City of Hope ( Site 0001), Duarte
Pacific Cancer Care ( Site 0006), Monterey
University of California San Francisco ( Site 0023), San Francisco
Rambam Medical Center ( Site 0382), Haifa
Chaim Sheba Medical Center. ( Site 0380), Ramat Gan
Sourasky Medical Center ( Site 0381), Tel Aviv
Hadassah Ein Karem Jerusalem ( Site 0383), Jerusalem
Dana Farber Cancer Institute ( Site 0002), Boston
BC Cancer ( Site 0107), Vancouver
CancerCare Manitoba ( Site 0101), Winnipeg
Princess Margaret Cancer Centre ( Site 0100), Toronto
Jewish General Hospital ( Site 0105), Montreal
Merck Sharp & Dohme LLC
INDUSTRY