A Phase 1/2 Study of BA3071 in Patients With Solid Tumors
Running, not enrolling · Phase 1/Phase 2
Conditions studied: NSCLC, Melanoma
In brief
The objective of this study is to assess safety and efficacy of BA3071 in solid tumors
Key facts
- Study ID
- NCT05180799
- Run by
- BioAtla, Inc.
- People needed
- 320
- Starts
- 2022-08-03
- Expected to finish
- 2026-06-30
- Last updated by the study team
- 2025-06-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients must have measurable disease.
- Age ≥ 18 years
- CLTA-4 blocking-antibody naïve
- Adequate renal function
- Adequate liver function
- Adequate hematological function
- Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Patients must have single or any combination of the following mutations: KRAS, STK11, KEAP1 and/or PD-L1 TPS <1%
- Patients must be eligible for surgery (NSCLC Stage IIB-IIIA only)
You may not qualify if…
- Patients must not have clinically significant cardiac disease.
- Patients must not have known non-controlled CNS metastasis.
- Patients must not have a history of ≥ Grade 3 allergic reactions to mAb therapy as well as known or suspected allergy or intolerance to any agent given during this study.
- Patients must not have had major surgery within 4 weeks before first BA3071 administration.
- Patients must not have known human immunodeficiency virus (HIV) infection, active hepatitis B and/or hepatitis C.
- Patients must not be women who are pregnant or breast feeding.
Where it is running
- 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
Full record on ClinicalTrials.gov
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