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A Phase 1/2 Study of BA3071 in Patients With Solid Tumors
Sponsor: BioAtla, Inc.
Summary
The objective of this study is to assess safety and efficacy of BA3071 in solid tumors
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
320
Start Date
2022-08-03
Completion Date
2026-06-30
Last Updated
2025-06-15
Healthy Volunteers
No
Interventions
BA3071
Conditionally active biologic (CAB) antibody that binds to CTLA-4
Nivolumab
Humanized, immunoglobulin G4 (IgG4)-variant mAb against PD-1
Pembrolizumab
Humanized antibody, immunoglobulin G4, with a variable region against the human PD-1 receptor
Pemetrexed (Alimta)
pemetrexed with either cisplatin or carboplatin
Locations (12)
The Angeles Clinic and Research Institute
Los Angeles, California, United States
USC Norris Comprehensive Cancer Center
Los Angeles, California, United States
Piedmont West
Atlanta, Georgia, United States
Northwest Cancer Centers
Dyer, Indiana, United States
Morristown Medical Center/Atlantic Health System
Morristown, New Jersey, United States
Icahn School of Medicine at Mt. Sinai
New York, New York, United States
University Hospitals Cleveland Medical Center
Cleveland, Ohio, United States
Providence Cancer Institute
Portland, Oregon, United States
University of Utah Huntsman Cancer Institute
Salt Lake City, Utah, United States
Border Medical Oncology Research Unit at Albury Wodonga Regional Cancer Centre
Albury, New South Wales, Australia
Cancer Care Foundation
Miranda, New South Wales, Australia
Cancer Research South Australia
Adelaide, South Australia, Australia