Spots Global Cancer Trial Database for Molecularly Targeted Therapy in Treating Patients With BRAF Wild-type Melanoma That is Metastatic
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Trial Identification
Brief Title: Molecularly Targeted Therapy in Treating Patients With BRAF Wild-type Melanoma That is Metastatic
Official Title: Stand Up to Cancer Consortium Genomics-Enabled Medicine for Melanoma (G.E.M.M.): Using Molecularly-Guided Therapy for Patients With BRAF Wild-Type (BRAFwt) Metastatic Melanoma
Study ID: NCT02094872
Study Description
Brief Summary: This phase II trial studies how well molecularly targeted therapy works in treating patients with melanoma that has spread to other parts of the body. Patients must have received or do not qualify for prior immunotherapy. Targeted therapy is a type of treatment that uses drugs or other substances to identify and attack specific types of cancer cells with less harm to normal cells. Molecularly targeted therapy works by treating patients with substances that kill cancer cells by targeting key molecules involved in cancer cell growth.
Detailed Description: PRIMARY OBJECTIVES: I. To determine the difference in best overall response rate (BORR) between patients treated with MEK162 following personalized molecularly guided assignment vs. a historical BORR of 7% in this patient population. SECONDARY OBJECTIVES: I. To evaluate the safety of performing individualized drug therapy (including novel agents and commercially-available agents) in the context of a personalized medicine clinical trial. II. To define the difference in progression free survival (PFS) between patients treated with MEK162 following personalized molecularly guided assignment vs. a historical PFS rate of 2 months in this patient population. III. To continually assess data in real time so as to iteratively refine and standardize a set of statistical and informatics methodologies for matching treatments to the patient's tumor, based on the molecular profile. OUTLINE: Patients undergo collection of tissue and blood samples for deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) analysis via sequencing. Based on the results of the DNA and RNA analysis, patients receive molecularly targeted therapy. Treatment continues in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up for 30 days.
Keywords
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
Mayo Clinic Cancer Center, Scottsdale, Arizona, United States
Smilow Cancer Hospital at Yale-New Haven, New Haven, Connecticut, United States
Mayo Clinic Cancer Center, Jacksonville, Florida, United States
University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan, United States
Barbara Ann Karmanos Cancer Institute, Detroit, Michigan, United States
Mayo Clinic Cancer Center, Rochester, Minnesota, United States
Vanderbilt University Medical Center, Nashville, Tennessee, United States
Baylor Sammons Cancer Center, Dallas, Texas, United States
Contact Details
Name: Patricia LoRusso, D.O.
Affiliation: Yale University
Role: PRINCIPAL_INVESTIGATOR
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