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Phase 1 Study Evaluating BA3182 in Patients With Advanced Adenocarcinoma.
RECRUITINGPhase 1Sponsored by BioAtla, Inc.
Actively Recruiting
PhasePhase 1
SponsorBioAtla, Inc.
Started2023-07-14
Est. completion2028-09-15
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations9 sites
View on ClinicalTrials.gov →
NCT05808634
Summary
The objective of this study is to assess safety and efficacy of BA3182 in Advanced Adenocarcinoma
Eligibility
Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria: * Histologically or cytologically confirmed locally advanced unresectable or metastatic adenocarcinoma * Age ≥ 18 years * Adequate renal function * Adequate liver function * Adequate hematological function * Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. Exclusion Criteria: * Patients must not have clinically significant cardiac disease. * Patients must not have known non-controlled CNS metastasis. * Patients must not have active autoimmune disease or a documented history of autoimmune disease. * Patients must not have a history of ≥ Grade 3 allergic reactions to mAb therapy as wellas known or suspected allergy or intolerance to any agent given during this study. * Patients must not incomplete recovery from the effects of major surgery or significant traumatic injury before the first dose of study treatment. * 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.
Conditions2
Advanced AdenocarcinomaCancer
Locations9 sites
UC Irvine
Irvine, California, 92697
USC Norris Comprehensive Cancer Center
Los Angeles, California, 90033
Northwestern University
Chicago, Illinois, 60611
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
PhasePhase 1
SponsorBioAtla, Inc.
Started2023-07-14
Est. completion2028-09-15
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations9 sites
View on ClinicalTrials.gov →
NCT05808634