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Brief Title: A Study of Novel Anti-cancer Agents in Patients With Metastatic Triple Negative Breast Cancer
Official Title: A Phase IB/II, 2-stage, Open-label, Multicenter Study to Determine the Efficacy and Safety of Durvalumab (MEDI4736) + Paclitaxel and Durvalumab (MEDI4736) in Combination With Novel Oncology Therapies With or Without Paclitaxel for First-line Metastatic Triple Negative Breast Cancer
Study ID: NCT03742102
Brief Summary: This study is designed to determine the efficacy and safety of durvalumab in combination with novel oncology therapies with or without paclitaxel and durvalumab + paclitaxel for first-line metastatic triple negative breast cancer
Detailed Description: This is a Phase IB/II, 2-stage, open-label, multicenter study to determine the efficacy and safety of durvalumab in combination with novel oncology therapies (i.e. therapies designed for immune modulation) with or without paclitaxel and durvalumab + paclitaxel as first-line treatment in patients with metastatic triple negative breast cancer (TNBC). The study is designed to concurrently evaluate potential novel treatment combinations with clinical promise using a 2-stage approach. The study will use a Simon 2-Stage design to evaluate which cohorts may proceed to expansion. Part 1 is a Phase IB study of safety and initial efficacy, and Part 2 may expand patient enrollment if adequate efficacy signal is observed in Part 1. The treatment regimens evaluated in Part 2 will depend on the evaluation of safety and efficacy outcomes in Part 1.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: FEMALE
Healthy Volunteers: No
Research Site, Goodyear, Arizona, United States
Research Site, Tucson, Arizona, United States
Research Site, West Hollywood, California, United States
Research Site, Columbia, Maryland, United States
Research Site, Boston, Massachusetts, United States
Research Site, Boston, Massachusetts, United States
Research Site, Grand Rapids, Michigan, United States
Research Site, Saint Paul, Minnesota, United States
Research Site, Saint Louis, Missouri, United States
Research Site, Las Vegas, Nevada, United States
Research Site, Eugene, Oregon, United States
Research Site, Philadelphia, Pennsylvania, United States
Research Site, Dallas, Texas, United States
Research Site, Flower Mound, Texas, United States
Research Site, Houston, Texas, United States
Research Site, McAllen, Texas, United States
Research Site, San Antonio, Texas, United States
Research Site, Fairfax, Virginia, United States
Research Site, Williamsburg, Virginia, United States
Research Site, Kelowna, British Columbia, Canada
Research Site, London, Ontario, Canada
Research Site, Toronto, Ontario, Canada
Research Site, Greenfield Park, Quebec, Canada
Research Site, Montreal, Quebec, Canada
Research Site, Seoul, , Korea, Republic of
Research Site, Seoul, , Korea, Republic of
Research Site, Seoul, , Korea, Republic of
Research Site, Gdańsk, , Poland
Research Site, Gliwice, , Poland
Research Site, Kraków, , Poland
Research Site, Lublin, , Poland
Research Site, Opole, , Poland
Research Site, Poznań, , Poland
Research Site, Rzeszów, , Poland
Research Site, Warszawa, , Poland
Research Site, Warszawa, , Poland
Research Site, Kaohsiung, , Taiwan
Research Site, Taichung, , Taiwan
Research Site, Tainan City, , Taiwan
Research Site, Taipei, , Taiwan
Research Site, Taipei, , Taiwan
Research Site, Taoyuan, , Taiwan
Research Site, Cambridge, , United Kingdom
Research Site, London, , United Kingdom
Research Site, London, , United Kingdom
Research Site, Manchester, , United Kingdom
Research Site, Oxford, , United Kingdom
Name: Peter Schmid, MD, PhD
Affiliation: Barts Cancer Institute
Role: PRINCIPAL_INVESTIGATOR