A Study to Evaluate Immunotherapy Combinations in Participants With Lung Cancer
NCT03846310 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 77
Last updated 2024-12-09
Summary
This is a Phase 1/1b, multicenter, open-label, dose-escalation and dose-expansion study to evaluate the safety, tolerability, pharmacokinetic (PK), pharmacodynamic, and clinical activity of etrumadenant (AB928) in combination with carboplatin and pemetrexed, with or without an anti-PD-1 antibody (pembrolizumab or zimberelimab), in participants with non-squamous Non-Small Cell Lung Cancer (NSCLC).
Conditions
- Non Small Cell Lung Cancer Metastatic
- Non Small Cell Lung Cancer
- Nonsquamous Nonsmall Cell Neoplasm of Lung
- Sensitizing EGFR Gene Mutation
Interventions
- DRUG
-
Etrumadenant
Etrumadenant is an A2aR and A2bR antagonist
- DRUG
-
Zimberelimab
Zimberelimab is a fully human anti-PD-1 monoclonal antibody
- DRUG
-
Carboplatin administered as part of standard chemotherapy regimen
- DRUG
-
Pemetrexed
Pemetrexed administered as part of standard chemotherapy regimen
- DRUG
-
Pembrolizumab is a humanized anti-PD-1 monoclonal antibody
Sponsors & Collaborators
- collaborator INDUSTRY
-
Arcus Biosciences, Inc.
lead INDUSTRY
Principal Investigators
-
Medical Director · Arcus Biosciences, Inc.
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-04-01
- Primary Completion
- 2024-11-18
- Completion
- 2024-11-18
- FDA Drug
- Yes
Countries
- United States
- Singapore
- South Korea
- Taiwan
Study Locations
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