Study on Platinum-Based Chemotherapy With or Without INCMGA00012 for Advanced Non-Small Cell Lung Cancer

Sponsor: Incyte Corporation

Sponsor score: 60
Inactive

ClinicalTrials ID:NCT04205812

This clinical trial is evaluating the effectiveness and safety of using platinum-based chemotherapy, with or without the addition of the drug INCMGA00012, in patients with advanced non-small cell lung cancer (NSCLC).

Patient Parameters

Program Overview

The aim of this study is to determine how well platinum-based chemotherapy works, with or without the drug INCMGA00012, in treating patients with advanced non-small cell lung cancer (NSCLC). The study will focus on both the effectiveness of the treatment and its safety for patients.

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with advanced non-small cell lung cancer (NSCLC), either squamous or nonsquamous type, at Stage IV.
  • Have not received any previous treatment for advanced or metastatic NSCLC.
  • Able to provide a sample of tumor tissue for testing.
  • Have at least one tumor that can be measured by scans.
  • Be in good overall health, with a performance status score of 0 or 1, meaning fully active or restricted in physically strenuous activity but ambulatory.
  • Have a life expectancy of at least 3 months.
  • Agree to use effective birth control to prevent pregnancy during the study.
  • Have good organ function as shown by specific lab tests.
  • Have been fully vaccinated against COVID-19 or be willing to get vaccinated during the study.

Exclusion Criteria

  • Have had serious heart problems within the last 6 months.
  • Have had major surgery within 3 weeks before starting the study treatment.
  • Have had high-dose radiation therapy to the chest within the last 6 months.
  • Have a history of nerve damage that could be worsened by certain chemotherapy drugs.
  • Have untreated cancer that has spread to the brain or spinal cord.
  • Have lung diseases that required treatment with steroids.
  • Have an active infection or tuberculosis that needs treatment.
  • Have certain types of superficial cancers or in situ cancers.
  • Have allergies or contraindications to the chemotherapy drugs used in the study.
  • Have an active autoimmune disease that needed treatment in the last 2 years.
  • Are taking antibiotics or steroids within 7 days before starting the study treatment.
  • Have received a live vaccine within 30 days before starting the study treatment.
  • Have active hepatitis B or C infections.

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