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Expanded Access for IMMU-132

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT04320693
Expanded Access Status : Approved for marketing
First Posted : March 25, 2020
Last Update Posted : August 19, 2021
Information provided by (Responsible Party):
Gilead Sciences

Brief Summary:
This is an expanded access program (EAP) for eligible participants designed to provide access to IMMU-132.

Condition or disease Intervention/treatment
Metastatic Triple-Negative Breast Carcinoma Drug: IMMU-132

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Study Type : Expanded Access
Expanded Access Type : Individual Patients
Official Title: Expanded Access for IMMU-132

Resource links provided by the National Library of Medicine

Intervention Details:
  • Drug: IMMU-132
    IMMU-132 will be administered as an intravenous infusion on Days 1 and 8 of 21-day treatment cycles
    Other Name: Sacituzumab Govitecan

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All

Inclusion Criteria:


Exclusion Criteria:


No Contacts or Locations Provided
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Responsible Party: Gilead Sciences Identifier: NCT04320693    
Other Study ID Numbers: IMMU-132
First Posted: March 25, 2020    Key Record Dates
Last Update Posted: August 19, 2021
Last Verified: April 2020
Additional relevant MeSH terms:
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Breast Neoplasms
Neoplasms by Site
Breast Diseases
Skin Diseases