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Brief Title: A Study of AB801 Monotherapy and Combination Therapy in Participants With Advanced Malignancies
Official Title: A Phase 1/1b Study to Evaluate the Safety and Tolerability of AB801 Monotherapy and Combination Therapy in Participants With Advanced Malignancies
Study ID: NCT06120075
Brief Summary: The primary purpose of this study is to assess the safety and tolerability of AB801 in participants with advanced malignancies, and to determine a recommended AB801 dose for expansion.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
START MIdwest, Grand Rapids, Michigan, United States
Icahn School of Medicine at Mount Sinai/ The Tisch Cancer Cente, New York, New York, United States
Mary Crowley, Dallas, Texas, United States
START - South Texas Accelerated Research Theraputics, LLC., San Antonio, Texas, United States
START Mountain Region, West Valley City, Utah, United States
Next Oncology Virginia, Fairfax, Virginia, United States
Name: Medical Director
Affiliation: Arcus Biosciences
Role: STUDY_DIRECTOR