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
| Parameter | Options |
|---|
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.
Get This Program In Your Inbox
Receive detailed information about this treatment opportunity to review with your healthcare provider.
