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Spots Global Cancer Trial Database for A Study of Novel Anti-cancer Agents in Patients With Metastatic Triple Negative Breast Cancer

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Trial Identification

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

Study Description

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.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

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

Contact Details

Name: Peter Schmid, MD, PhD

Affiliation: Barts Cancer Institute

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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