125
Participants
Start Date
December 29, 2020
Primary Completion Date
June 2, 2023
Study Completion Date
June 2, 2023
CX-2009
Intravenous administration of the CX-2009 of 6 mg/kg administered every 3 weeks (Q3W)
CX-072
Intravenous administration of the CX-072 of 1200 mg administered every 3 weeks (Q3W)
Montefiore Medical Center, The Bronx
Seoul National University Bundang Hospital, Seongnam-si
UPMC Magee-Womens Hospital, Pittsburgh
University of Maryland, Baltimore
Gachon University Gil Medical Center, Incheon
Virginia Cancer Specialists, Fairfax
Hospital Universitario Ramn y Cajal, Madrid
Hospital Universitario HM Sanchinarro, Madrid
NEXT Oncology, Madrid
MUSC, Charleston
Baptist Medical Center, Jacksonville
FCS - North, St. Petersburg
FCS - South, Fort Myers
Hematology Oncology Assoc of the Treasure Coast, Port Saint Lucie
Tennessee Oncology, Nashville
Cleveland Clinic, Cleveland
Hospital Clinico Universitario de Valencia, Valencia
Indiana University Health Melvin and Bren Simon Cancer Center, Indianapolis
University of Wisconsin, Madison
Allina Health System, Minneapolis
University of Chicago Medical Center, Chicago
Nebraska Cancer Specialists, Omaha
UT Health East Texas HOPE Cancer Center, Tyler
Hematology Oncology Clinic, Baton Rouge
Rocky Mountain Cancer Centers, Lone Tree
Huntsman Cancer Institute Research, Salt Lake City
Los Angeles Hematology Oncology Medical, Los Angeles
USC Norris Cancer Center, Los Angeles
UCLA David Geffen, Santa Monica
Moores Cancer Center, La Jolla
Summit Cancer Centers, Spokane
MGH, Boston
DRCI, Boston
Soon Chun Hyang University Cheonan Hospital SCHMC, Cheonan
Korea University Anam Hospital, Seoul
Asan Medical Center, Seoul
Gangnam Severance Hospital, Seoul
Samsung Medical Center, Seoul
Hospital Clinic i Provincial de Barcelona, Barcelona
Vall d'Hebron University Hospital, Barcelona
Institut Catala Oncologia, Barcelona
Hospital Parc Tauli, Sabadell
Lead Sponsor
CytomX Therapeutics
INDUSTRY