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NCT05180799

A Phase 1/2 Study of BA3071 in Patients With Solid Tumors

Active, enrolled Phase 1, PHASE2 Last updated 15 June 2025
What this trial tests

Phase 1, PHASE2 trial testing BA3071 in NSCLC in 320 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
3 August 2022
Primary endpoint
19 March 2025
30 June 2026

Quick facts

Lead sponsorBioAtla, Inc.
PhasePhase 1, PHASE2
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment320
Start date3 August 2022
Primary completion19 March 2025
Estimated completion30 June 2026
Sites12 locations across United States, Australia

Drugs / interventions tested

Conditions studied

Sponsor

BioAtla, Inc. — full company profile →

Who can join

18 and older, any sex, with NSCLC or Melanoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to assess safety and efficacy of BA3071 in solid tumors

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Dual blockade immunotherapy targeting PD-1/PD-L1 and CTLA-4 in lung cancer.
    Cheng W, Kang K, Zhao A, Wu Y. · · 2024 · cited 110× · PMID 39068460 · DOI 10.1186/s13045-024-01581-2

Verify or expand the search:

Other recruiting trials for NSCLC

Currently open trials in the same condition.

Other BioAtla, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05180799.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing