[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

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Study’s contact

Call center

855-907-3286

Email address

Clinical.Trials@bms.com

Condition

Non-Small Cell Lung Cancer

Treatment type

Interventional

Investigational product

BMS-986207

Phase

Phase 2

Sponsor

Bristol-Myers Squibb

ClinicalTrials.gov identifier

NCT05005273

Study number

CA020016

Understanding clinical trials

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About the study

The purpose of this study is to determine the safety and efficacy of BMS-986207 in combination with nivolumab and ipilimumab as first-line treatment for participants with stage IV non-small cell lung cancer (NSCLC).

Who can take part?

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

Inclusion criteria

  1. Histologically confirmed metastatic 1L Stage IV non-small cell lung cancer (NSCLC) of squamous or nonsquamous histology
  2. No prior systemic anti-cancer treatment given as primary therapy for advanced or metastatic NSCLC
  3. Measurable disease as per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1
  4. Eastern Cooperative Oncology Group (ECOG) performance status 0-1
  5. A formalin-fixed, paraffin-embedded (FFPE) tumor tissue block or a minimum of 20 unstained slides of tumor tissue obtained during screening or prior to enrollment
  6. Life expectancy of at least 3 months at the time of first dose
Exclusion criteria

  1. Participants with epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), or c-ros oncogene 1 (ROS-1) mutations which are sensitive to available targeted inhibitor therapy. Participants with nonsquamous histology and unknown EGFR, ALK, or ROS-1 status are also excluded
  2. Participants with known B-rapidly accelerated fibrosarcoma proto-oncogene (BRAF) V600E mutations that are sensitive to available targeted inhibitor therapy. Participants with unknown or indeterminate BRAF mutation status are eligible.
  3. Untreated central nervous system metastases
  4. Leptomeningeal metastases (carcinomatous meningitis)
  5. Concurrent malignancy requiring treatment
  6. Active, known, or suspected autoimmune disease
  7. Interstitial lung disease
  8. Uncontrolled or significant cardiovascular disease Other protocol-defined inclusion/exclusion criteria apply

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.

Find a Study Site