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Spots Global Cancer Trial Database for Nivolumab in Combination With Ipilimumab (Part 1); Nivolumab Plus Ipilimumab in Combination With Chemotherapy (Part 2) as First Line Therapy in Stage IV Non-Small Cell Lung Cancer

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Trial Identification

Brief Title: Nivolumab in Combination With Ipilimumab (Part 1); Nivolumab Plus Ipilimumab in Combination With Chemotherapy (Part 2) as First Line Therapy in Stage IV Non-Small Cell Lung Cancer

Official Title: A Study of Nivolumab in Combination With Ipilimumab (Part 1); and Nivolumab Plus Ipilimumab in Combination With Chemotherapy (Part 2) as First Line Therapy in Stage IV Non-Small Cell Lung Cancer (NSCLC)

Study ID: NCT02659059

Study Description

Brief Summary: The purpose of part 1 of this study is to determine the objective response rate (ORR) in stage IV NSCLC subjects treated with nivolumab in combination with ipilimumab as first line therapy. The purpose of part 2 of this study is to determine the safety and tolerability of nivolumab and ipilimumab combined with a short course of chemotherapy in first line stage IV NSCLC.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Sharp Memorial Hospital, San Diego, California, United States

Cancer Center Of Central Connecticut, Plainville, Connecticut, United States

Cleveland Clinic Florida, Weston, Florida, United States

Winship Cancer Institute., Atlanta, Georgia, United States

Summit Cancer Care, Savannah, Georgia, United States

Cancer Center Of Kansas, Wichita, Kansas, United States

University Of Louisville Medical Center, Inc., Dba, Louisville, Kentucky, United States

Johns Hopkins Cancer Center, Baltimore, Maryland, United States

Local Institution - 0029, Boston, Massachusetts, United States

Local Institution - 0030, Boston, Massachusetts, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Henry Ford Health System, Detroit, Michigan, United States

Local Institution - 0015, Lincoln, Nebraska, United States

Hackensack University Medical Center, Hackensack, New Jersey, United States

Local Institution - 0036, Albuquerque, New Mexico, United States

Lovelace Cancer Care, Albuquerque, New Mexico, United States

New Mexico Cancer Care Alliance, Albuquerque, New Mexico, United States

New Mexico Cancer Care Center, Albuquerque, New Mexico, United States

The Cancer Center at Presbyterian, Albuquerque, New Mexico, United States

Local Institution - 0010, Mineola, New York, United States

Memorial Sloan Kettering Nassau, New York, New York, United States

Duke University, Durham, North Carolina, United States

Novant Health Oncology Specialists, Winston-Salem, North Carolina, United States

The Ohio State University, Columbus, Ohio, United States

Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States

Local Institution - 0006, Pittsburgh, Pennsylvania, United States

Charleston Hematology Oncology Associates, Pa, Charleston, South Carolina, United States

Tennessee Oncology, PLLC - SCRI - PPDS, Nashville, Tennessee, United States

Vanderbilt University Medical Center, Nashville, Tennessee, United States

Local Institution - 0022, Kingston, Ontario, Canada

Local Institution - 0023, Sault Ste Marie, Ontario, Canada

Csss De St-Jerome, St. Jerome, Quebec, Canada

Contact Details

Name: Bristol-Myers Squibb

Affiliation: Bristol-Myers Squibb

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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