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Clinical Trial Details — Status: No longer available

Administrative data

NCT number NCT02186249
Other study ID # CA209-218
Secondary ID
Status No longer available
Phase N/A
First received July 8, 2014
Last updated February 6, 2017

Study information

Verified date February 2017
Source Bristol-Myers Squibb
Contact n/a
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

The purpose of this study is to provide treatment with nivolumab in combination with ipilimumab to subjects who are anti-(CTLA)-4 and anti-PD-1 treatment-naive and have unresectable or metastatic melanoma.


Recruitment information / eligibility

Status No longer available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com

Inclusion Criteria:

- Men and women 18 years and older

- Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1

- Histologically-confirmed unresectable stage III or stage IV melanoma, as per American Joint Committee on Cancer (AJCC) staging system, Including mucosal and ocular melanoma

- Subjects must be anti-CTLA-4 treatment-naive and anti-PD-1 treatment-naive. Subjects may have had other prior systemic treatment for localized or metastatic disease

- Subjects with brain metastases are eligible if these have been treated and there is no magnetic resonance imaging (MRI) evidence of progression for at least 2 weeks after treatment is complete and within 28 days prior to first dose of study drug administration. There must also be no requirement for high doses of systemic corticosteroids that could result in Immunosuppression (>10 mg/day prednisone equivalent) for at least 2 weeks prior to study drug administration

Exclusion Criteria:

- Active (symptomatic) and not treated brain metastases or leptomeningeal metastases

- Life expectancy < 6 weeks

- Subjects with active, known, or suspected autoimmune disease. Subjects with Type I diabetes mellitus, hypothyroidism only requiring hormone replacement, skin disorders (such as vitiligo, psoriasis, or alopecia) not requiring systemic treatment, or conditions not expected to recur in absence of an external trigger are permitted to enroll

- Subjects with a condition requiring systemic treatment with either corticosteroids (>10 mg daily prednisone equivalents) or other immunosuppressive medications within 14 days of treatment. Inhaled or topical steroids and adrenal replacement steroid doses > 10 mg daily prednisone equivalent are permitted in the absence of active autoimmune disease

- Subjects who received prior therapy with an anti-CTLA-4, anti-PD-1, anti-PD-L1 or anti-PD-L2, anti-CT137 (or any other antibody or drug specifically targeting T-cell costimulation or checkpoint pathways) or subject is expected to require any other form of systemic antineoplastic therapy while receiving nivolumab

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Nivolumab

Ipilimumab


Locations

Country Name City State
Canada Cross Cancer Institute Edmonton Alberta
Canada Grand River Hospital Kitchener Ontario
Canada London Health Sciences Centre London Ontario
Canada McGill University Health Center Montreal Quebec
Canada Lakeridge Health Oshawa Oshawa Ontario
Canada Chuq Centre Hospitalier Universitaire de Quebec Quebec
Canada Princess Margaret Hospital Toronto Ontario
Canada Sunnybrook Health Science Centre Toronto Ontario
Canada British Columbia Cancer Agency Vancouver British Columbia
United States Lehigh Valley Health Network Allentown Pennsylvania
United States University of Michigan Comprehensive Cancer Center Ann Arbor Michigan
United States Winship Cancer Institute Atlanta Georgia
United States University of Colorado Hospital Aurora Colorado
United States Texas Oncology Austin Texas
United States 6501 Truxtun Avenue Bakersfield California
United States Johns Hopkins Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland
United States Medstar Health Research Institute Baltimore Maryland
United States Center For Cancer and Blood Disorders Bethesda Maryland
United States St Luke's Hospital Bethlehem Pennsylvania
United States Beth Israel Deaconess Medical Center Boston Massachusetts
United States Dana Farber Cancer Institute Boston Massachusetts
United States Massachusetts General Hospital Boston Massachusetts
United States Carolinas Healthcare System Charlotte North Carolina
United States Karmanos Cancer Institute Detroit Michigan
United States Greenville Health System Easley South Carolina
United States Evanston Premier Healthcare Research LLC Evanston Illinois
United States Banner MD Anderson Cancer Center Gilbert Arizona
United States Cancer and Hematology Centers of Western Michigan Grand Rapids Michigan
United States Memorial Regional Hospital Hollywood Florida
United States MD Anderson Cancer Center Houston Texas
United States 4500 San Pablo Road South Jacksonville Florida
United States Cancer Specialists of North Florida Jacksonville Florida
United States UC San Diego Moores Cancer Center La Jolla California
United States Comprehensive Cancer Centers of Nevada Las Vegas Nevada
United States Rocky Mountain Cancer Centers Littleton Colorado
United States UF Health Cancer Center at Orlando Health Longwood Florida
United States 100 UCLA Medical Plaza Los Angeles California
United States Local Institution Louisville Kentucky
United States University of Wisconsin Madison Wisconsin
United States Mount Sinai Medical Center Miami Beach Florida
United States Texas Oncology Midland Texas
United States Atlantic Health System Morristown New Jersey
United States Tennessee Oncology PLLC Nashville Tennessee
United States Smilow Cancer Hospital at Yale University Cancer Center New Haven Connecticut
United States Memorial Sloan-Kettering Cancer Center New York New York
United States NYU Langone Medical Center New York New York
United States 600 Celebrate Life Parkway Newnan Georgia
United States Oncology Specialists, SC Niles Illinois
United States Florida Hospital Cancer Institute Orlando Florida
United States Texas Oncology Paris Texas
United States Mayo Clinic Arizona Phoenix Arizona
United States Northwest Cancer Specialists PC Portland Oregon
United States 514 North Prospect Ave Redondo Beach California
United States Virginia Cancer Institute Richmond Virginia
United States Oncology and Hematology Associates of Southwest Virginia, Inc Roanoke Virginia
United States Mayo Clinic Rochester Minnesota
United States Washington University School of Medicine Saint Louis Missouri
United States California Pacific Medical Center Research Institute San Francisco California
United States University of California San Francisco San Francisco California
United States 1325 East Church Street Santa Monica California
United States Angeles Clinic and Research Institute Santa Monica California
United States Seattle Cancer Care Alliance Seattle Washington
United States H. Lee Moffitt Cancer Center & Research Institute Tampa Florida
United States Tulsa Cancer Institute PLLC Tulsa Oklahoma
United States Georgetown-Lombardi Comprehensive Cancer Center Washington District of Columbia
United States Shenandoah Oncology Association Winchester Virginia

Sponsors (1)

Lead Sponsor Collaborator
Bristol-Myers Squibb

Countries where clinical trial is conducted

United States,  Canada, 

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