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Brief Title: Ipilimumab With or Without Talimogene Laherparepvec in Unresected Melanoma
Official Title: Phase 1b/2, Multicenter, Open-label Trial to Evaluate the Safety and Efficacy of Talimogene Laherparepvec and Ipilimumab Compared to Ipilimumab Alone in Subjects With Unresected, Stage IIIB-IV Melanoma
Study ID: NCT01740297
Brief Summary: Phase 1b of the study will evaluate the safety of talimogene laherparepvec in combination with ipilimumab. Phase 2 is a randomized study that will evaluate the safety and efficacy of talimogene laherparepvec in combination with ipilimumab versus ipilumumab alone.
Detailed Description: The phase 1b part is an open-label, multicenter, single-arm study where all participants will receive talimogene laherparepvec in combination with ipilimumab. The phase 2 part of the study is an open-label, multicenter, randomized study to further assess the safety and to evaluate the efficacy of talimogene laherparepvec in combination with ipilimumab. Participants will be randomized 1:1 to receive talimogene laherparepvec plus ipilimumab or ipilimumab alone. Participants randomized before amendment 2 will be stratified by stage of disease (stage IIIB/C, IVM1a, and stage IVM1b vs IVM1c) and v-raf murine sarcoma viral oncogene homolog B1 (BRAF) V600E (a mutation resulting in a substitution of glutamic acid for valine at codon 600) (mutation vs mutation not present). Participants randomized after amendment 2 will be stratified by stage of disease (stage IIIB/C and IVM1a vs stage IVM1b and IVM1c) and prior therapy (treatment naïve vs previously treated with systemic anticancer immunotherapy vs previously treated with systemic anticancer treatment other than immunotherapy).
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Research Site, Tucson, Arizona, United States
Research Site, Beverly Hills, California, United States
Research Site, Los Angeles, California, United States
Research Site, Los Angeles, California, United States
Research Site, Los Angeles, California, United States
Research Site, San Francisco, California, United States
Research Site, Santa Rosa, California, United States
Research Site, Aurora, Colorado, United States
Research Site, Jacksonville, Florida, United States
Research Site, Jacksonville, Florida, United States
Research Site, Lakeland, Florida, United States
Research Site, Miami, Florida, United States
Research Site, Chicago, Illinois, United States
Research Site, Indianapolis, Indiana, United States
Research Site, Indianapolis, Indiana, United States
Research Site, Iowa City, Iowa, United States
Research Site, Louisville, Kentucky, United States
Research Site, Minneapolis, Minnesota, United States
Research Site, Saint Louis, Missouri, United States
Research Site, Morristown, New Jersey, United States
Research Site, New Brunswick, New Jersey, United States
Research Site, New York, New York, United States
Research Site, New York, New York, United States
Research Site, Chapel Hill, North Carolina, United States
Research Site, Canton, Ohio, United States
Research Site, Cincinnati, Ohio, United States
Research Site, Charleston, South Carolina, United States
Research Site, Nashville, Tennessee, United States
Research Site, Houston, Texas, United States
Research Site, Salt Lake City, Utah, United States
Research Site, Richmond, Virginia, United States
Research Site, Milwaukee, Wisconsin, United States
Research Site, Bordeaux, , France
Research Site, Grenoble Cedex 9, , France
Research Site, Lille, , France
Research Site, Nantes Cedex 1, , France
Research Site, Paris, , France
Research Site, Göttingen, , Germany
Research Site, Kiel, , Germany
Research Site, Tübingen, , Germany
Name: MD
Affiliation: Amgen
Role: STUDY_DIRECTOR