Sacituzumab Govitecan In TNBC

2020-01-22 12:12:55 | BioPortfolio


This research study is studying to see if Sacituzumab govitecan is effective and safe for individuals with localized triple negative breast cancer (TNBC)

The names of the study drugs involved in this study is:

- Sacituzumab govitecan


This research study is a Phase II clinical trial. Phase II clinical trials test the safety and effectiveness of an investigational drug to learn whether the drug works in treating a specific disease."Investigational" means that the drug is being studied.

This research study involves an experimental study treatment. The names of the study drugs involved in this study is:

- Sacituzumab govitecan

The research study procedures include screening for eligibility and study treatment including evaluations and follow up visits.

- Eligible participants will receive Sacituzumab govitecan for up to 12 weeks.

- This can be followed by standard chemotherapy at the discretion of the treating physician.

- It is expected that about 50 people will take part in this research study.

The U.S. Food and Drug Administration (FDA) has not approved Sacituzumab govitecan as a treatment for any disease.

Sacituzumab govitecan is an antibody-drug conjugate which means it's made up of an antibody attached to an anticancer drug. An antibody is a protein normally made the immune system. Sacituzumab govitecan is believed to work by binding the antibody portion of the drug in the tumor(s) while the anticancer drug portion works to prevent ancer cells from growing/spreading.

Study Design


Invasive Breast Cancer


Sacituzumab Govitecan


Beth Israel Deaconess Medical Center
United States


Not yet recruiting


Massachusetts General Hospital

Results (where available)

View Results


Published on BioPortfolio: 2020-01-22T12:12:55-0500

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