Phase II Safety Study of Vemurafenib Followed by Ipilimumab in Subjects With V600 BRAF Mutated Advanced Melanoma



Status:Completed
Conditions:Skin Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:Any
Updated:7/26/2018
Start Date:September 13, 2012
End Date:May 12, 2015

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A Single Arm Open-Label Phase II Study of Vemurafenib Followed by Ipilimumab in Subjects With Previously Untreated V600 BRAF Mutated Advanced Melanoma

The purpose of this study is to assess the safety profile of vemurafenib, 960 mg,
administered for 6 weeks, followed by ipilimumab monotherapy in patients with BRAF V600
mutated advanced/metastatic melanoma.


For more information regarding BMS clinical trial participation, please visit
www.BMSStudyConnect.com

Key Inclusion Criteria:

- Men and women 18 years of age and older

- Histologic diagnosis of malignant melanoma tested positive for the BRAF V600 mutation

- Previously untreated unresectable Stage III or Stage IV melanoma

- Complete set of brain/neck, chest, abdomen/pelvis axial radiographs taken within 28
days of first dose of study drug

- Measurable melanoma by physical or radiographic examination

- Brain metastases stable after radiation for at least 1 month and off corticosteroid
therapy for ≥30 days prior to enrollment

- Eastern Cooperative Oncology Group performance status of 0 or 1

- Adequate hematologic parameters and renal and hepatic function

Key Exclusion Criteria:

- Primary ocular melanoma

- Active brain metastases with symptoms or requiring corticosteroid treatment

- Any other malignancy from which the patient has been disease-free for less than 2
years, with the exception of adequately treated and cured basal or squamous cell skin
cancer, superficial bladder cancer, or carcinoma in situ of the cervix

- History of or current active autoimmune diseases, including but not limited to
inflammatory bowel diseases, rheumatoid arthritis, autoimmune thyroiditis, autoimmune
hepatitis, systemic sclerosis, systemic lupus erythematosus, autoimmune vasculitis,
autoimmune neuropathies

- History of or current immunodeficiency disease, splenectomy, or splenic irradiation

- Prior anticancer therapy or investigational products <4 weeks prior to enrollment

- Prior therapy with a BRAF or MEK inhibitor and prior investigational anticancer
immunotherapies;

- Prior therapies with immunosuppressive agents within the past 2 years

- Concomitant therapy with any anticancer or potent immunosuppressive agent, surgery,
radiotherapy, other investigational anticancer therapies, or chronic use of systemic
corticosteroids
We found this trial at
14
sites
Atlanta, Georgia 30322
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1201 Camino de Salud Northeast
Albuquerque, New Mexico 87131
(505) 272-4946
University of New Mexico Cancer Center It’s been 40 years since the New Mexico State...
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24 Sturtevant St
Orlando, Florida 32806
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Orlando, FL
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Beverly Hills, California 90211
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Beverly Hills, CA
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450 Brookline Ave
Boston, Massachusetts 2215
617-632-3000
Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...
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Boston, MA
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450 Brookline Ave
Boston, Massachusetts 2215
617-632-3000
Dana-Farber Cancer Institute Since it’s founding in 1947, Dana-Farber has been committed to providing adults...
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Boston, MA
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Charlotte, North Carolina 28211
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Charlotte, NC
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11100 Euclid Ave
Cleveland, Ohio 44106
(216) 844-1000
University Hospitals of Cleveland The history of University Hospitals Case Medical Center is linked to...
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Cleveland, OH
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Cleveland, Ohio 44106
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Detroit, Michigan 48201
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Detroit, MI
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Durham, North Carolina 27710
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Durham, NC
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Durham, North Carolina 27705
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Durham, NC
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Jacksonville, Florida
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Jacksonville, FL
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New York, New York 10029
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New York, NY
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