About the study

The purpose of this study is to assess the efficacy and safety of INCMGA00012 in combination with chemoradiation therapy (CRT) in participants with unresectable, Stage III non-small cell lung cancer (NSCLC). The study will randomize approximately 360 participants in a 2:1 ratio into the INCMGA00012 in combination with CRT followed by consolidation therapy with INCMGA00012 treatment group and placebo in combination with CRT followed by consolidation therapy with placebo treatment group.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria

1. Histologically or cytologically confirmed NSCLC that is locally advanced and unresectable.
2. Adequate tumor sample from fresh biopsy or archival tissue block must be available.
3. Evaluable disease per RECIST v1.1.
4. Eastern Cooperative Oncology Group performance status 0 to 1.
5. Willingness to avoid pregnancy or fathering children.

Exclusion criteria

1. Receipt of cancer treatment for this malignancy, including but not limited to radiation therapy, investigational agents, chemotherapy, and immunotherapy for disease under consideration.
2. Recent major surgery within 4 weeks before entry into the study.
3. Any medical contraindication to platinum-based doublet chemotherapy.
4. Active autoimmune disease requiring systemic immunosuppression in excess of physiologic consolidation doses of corticosteroids (> 10 mg/day of prednisone or equivalent).
5. Known hypersensitivity to another monoclonal antibody that cannot be controlled with standard measures (eg, antihistamines and corticosteroids).
6. Mixed small cell and NSCLC histology.
7. Evidence of interstitial lung disease or active noninfectious pneumonitis.
8. Participants who are HIV-positive.
9. History of organ transplant, including allogeneic stem cell transplantation.

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

Determine if a study site for this clinical trial is near you. Contact the study to apply.