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Brief Title: A Phase 1, Dose Finding Study of CC-90002 in Subjects With Advanced Solid and Hematologic Cancers
Official Title: A Phase I, Open-Label, Dose Finding Study of CC-90002, a Monoclonal Antibody Directed Against CD47, in Subjects With Advanced Solid and Hematologic Cancers
Study ID: NCT02367196
Brief Summary: CC-90002-ST -001 is an open-label, Phase 1, dose escalation clinical study in subjects with advanced, refractory solid and hematologic cancers.
Detailed Description: CC-90002-ST-001 is an open-label, Phase 1, dose escalation, first in human (FIH) clinical study of CC-90002, administered by intravenous (IV) infusion, in subjects with advanced, refractory solid and hematologic cancers. The study will be conducted in two parts. Part A dose escalation phase will explore escalating dose cohorts of the study drug CC-90002. Part B dose escalation will explore escalating doses of CC-90002 in combination with rituximab in subjects with CD20-positive NHL.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Scottsdale Healthcare Research Institute, Scottsdale, Arizona, United States
University of Arizona Cancer Center, Tucson, Arizona, United States
University of California San Francisco, San Francisco, California, United States
Yale University School of Medicine, New Haven, Connecticut, United States
South Texas Accelerated Research Therapeutics, San Antonio, Texas, United States
Hospital Universitari Germans Trias i Pujol Can Ruti, Badalona (Barcelona), , Spain
Hospital Val d'Hebron, Barcelona, , Spain
Duran i Reynals Institut Catala d'Oncologia, Barcelona, , Spain
Hospital Universitario Fundacion Jimenez Diaz, Madrid, , Spain
Hospital 12 de Octubre, Madrid, , Spain
Hospital Universitario de Salamanca, Salamanca, , Spain
Hospital Marques de Valdecilla, Santander, , Spain
Hospital de la Fe, Valencia, , Spain
Name: Michael Burgess, MD, PhD
Affiliation: Celgene
Role: STUDY_DIRECTOR