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Spots Global Cancer Trial Database for A Phase 1, Dose Finding Study of CC-90002 in Subjects With Advanced Solid and Hematologic Cancers

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Trial Identification

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

Interventions

CC-90002
Rituximab

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Name: Michael Burgess, MD, PhD

Affiliation: Celgene

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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