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Spots Global Cancer Trial Database for A Phase 1b Study of T-DXd Combinations in HER2-low Advanced or Metastatic Breast Cancer

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Trial Identification

Brief Title: A Phase 1b Study of T-DXd Combinations in HER2-low Advanced or Metastatic Breast Cancer

Official Title: A Phase 1b Multicentre, Open-label, Modular, Dose-finding and Dose-expansion Study to Explore the Safety, Tolerability, Pharmacokinetics and Anti-tumour Activity of Trastuzumab Deruxtecan (T-DXd) in Combination With Other Anti-cancer Agents in Patients With Metastatic HER2-low Breast Cancer (DESTINY-Breast08)

Study ID: NCT04556773

Study Description

Brief Summary: DESTINY-Breast 08 will investigate the safety, tolerability, PK and preliminary anti-tumour activity of T-DXd in combination with other therapies in patients with Metastatic HER2-low Advanced or Metastatic Breast Cancer

Detailed Description: This study is modular in design allowing assessment of the safety, tolerability, PK and preliminary anti-tumour activity of T-DXd in combination with other therapies. Combination-treatment modules will have 2 parts: a dose-finding phase (Part 1), and a dose expansion phase (Part 2); the Part 2 dose-expansion phase will use the RP2D determined in Part 1. The target population of interest in this study is patients with HER2-low (IHC 1+ or IHC 2+/ISH -) (as per ASCO/CAP 2018 guidelines) advanced/MBC. Part 1 of each module will enroll patients with locally confirmed HER2-low advanced/MBC in second-line or later (≥ 2L) settings Part 2 of each module will enroll patients with HER2-low MBC who have either not received prior treatment, or received only 1 prior treatment (depending on the module-specific exclusion criteria) for advanced/metastatic disease

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Research Site, Commack, New York, United States

Research Site, Harrison, New York, United States

Research Site, New York, New York, United States

Research Site, New York, New York, United States

Research Site, Uniondale, New York, United States

Research Site, Chapel Hill, North Carolina, United States

Research Site, Chattanooga, Tennessee, United States

Research Site, Germantown, Tennessee, United States

Research Site, Fort Worth, Texas, United States

Research Site, East Melbourne, , Australia

Research Site, Westmead, , Australia

Research Site, Edegem, , Belgium

Research Site, Leuven, , Belgium

Research Site, Ottignies, , Belgium

Research Site, Goiania, , Brazil

Research Site, Porto Alegre, , Brazil

Research Site, Porto Alegre, , Brazil

Research Site, Sao Paulo, , Brazil

Research Site, São Paulo, , Brazil

Research Site, Kelowna, British Columbia, Canada

Research Site, Quebec, , Canada

Research Site, Villejuif Cedex, , France

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, Monterrey, , Mexico

Research Site, Moscow, , Russian Federation

Research Site, Moscow, , Russian Federation

Research Site, Saint Petersburg, , Russian Federation

Research Site, Kaohsiung, , Taiwan

Research Site, Taichung, , Taiwan

Research Site, Taipei City, , Taiwan

Research Site, Taipei, , Taiwan

Research Site, Taipei, , Taiwan

Research Site, Taipei, , Taiwan

Research Site, Taoyuan, , Taiwan

Contact Details

Name: Komal Jhaveri, MD, FACP

Affiliation: Memorial Sloan Kettering Cancer Center

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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