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Spots Global Cancer Trial Database for ARX788 in HER2-positive, Metastatic Breast Cancer Subjects (ACE-Breast-03)

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Trial Identification

Brief Title: ARX788 in HER2-positive, Metastatic Breast Cancer Subjects (ACE-Breast-03)

Official Title: A Global, Phase 2 Study of ARX788 in HER2-positive Metastatic Breast Cancer Patients Who Were Previously Treated With T-DXd

Study ID: NCT04829604

Interventions

ARX788

Study Description

Brief Summary: A Global, Phase 2 Study of ARX788 in HER2-positive Metastatic Breast Cancer Patients who were previously treated with T-DXd

Detailed Description: A Global, Single Arm, Phase 2 Study of ARX788 in HER2-positive Metastatic Breast Cancer Patients who were previously treated with T-DXd. The ARX788 will be administered every 3 weeks (Q3W) intravenous (IV) infusion.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Research Site, Los Angeles, California, United States

Research Site, Los Angeles, California, United States

Research Site, Newport Beach, California, United States

Research Site, San Francisco, California, United States

Research Site, Santa Barbara, California, United States

Research Site, Torrance, California, United States

Research Site, West Los Angeles, California, United States

Research Site, Whittier, California, United States

Research Site, Newark, Delaware, United States

Research Site, Hollywood, Florida, United States

Research Site, Orlando, Florida, United States

Research Site, Athens, Georgia, United States

Research Site, Atlanta, Georgia, United States

Research Site, Chicago, Illinois, United States

Research Site, Louisville, Kentucky, United States

Research Site, Baton Rouge, Louisiana, United States

Research Site, Lutherville, Maryland, United States

Research Site, Silver Spring, Maryland, United States

Research Site, Boston, Massachusetts, United States

Research Site, Bolivar, Missouri, United States

Research Site, Saint Louis, Missouri, United States

Research Site, Omaha, Nebraska, United States

Research Site, Las Vegas, Nevada, United States

Research Site, Albuquerque, New Mexico, United States

Research Site, New York, New York, United States

Research Site, New York, New York, United States

Research Site, Portland, Oregon, United States

Research Site, Tigard, Oregon, United States

Research Site, Chattanooga, Tennessee, United States

Research Site, Nashville, Tennessee, United States

Research Site, Austin, Texas, United States

Research Site, Dallas, Texas, United States

Research Site, Houston, Texas, United States

Research Site, Plano, Texas, United States

Research Site, Tyler, Texas, United States

Research Site, Norfolk, Virginia, United States

Research Site, Tacoma, Washington, United States

Research Site, South Brisbane, Queensland, Australia

Research Site, Woolloongabba, Queensland, Australia

Research Site, Clayton, Victoria, Australia

Research Site, Frankston, Victoria, Australia

Research Site, Geelong, Victoria, Australia

Research Site, Melbourne, Victoria, Australia

Research Site, Ringwood East, Victoria, Australia

Research Site, Nedlands, Western Australia, Australia

Research Site, Avignon Cedex 09, , France

Research Site, La Rochelle, , France

Research Site, Le Mans, , France

Research Site, Nice, , France

Research Site, Toulouse CEDEX 9, , France

Research Site, Daegu, , Korea, Republic of

Research Site, Goyang-si, , Korea, Republic of

Research Site, Seongnam-si, , Korea, Republic of

Research Site, Seoul, , Korea, Republic of

Research Site, Seoul, , Korea, Republic of

Research Site, Seoul, , Korea, Republic of

Research Site, Seoul, , Korea, Republic of

Research Site, Suwon, , Korea, Republic of

Contact Details

Name: Ambrx

Affiliation: Ambrx, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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