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A Real World Study: Clinical Outcomes and Safety of Sacituzumab Govitecan in Metastatic HER-2 Negative Breast Cancer Patients

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

Clinical Outcomes and Safety of Sacituzumab Govitecan in Metastatic HER-2 negative Breast Cancer Patients

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Male or female aged 18 or above;

• The Eastern Cooperative Oncology Group (ECOG) physical condition score of the United States is ≤2;

• Unresectable or metastatic triple-negative breast cancer confirmed by tumor histology or cytology, and having received at least two systemic treatments previously (at least one of which was for metastatic disease); Or HR+/HER2- (IHC 0, 1+ or IHC 2+/ISH-) unresectable or metastatic breast cancer confirmed by tumor histology or cytology, with previous endocrine therapy and ≥2 lines of systemic therapy (for metastatic disease);

• Receive gosatetuzumab treatment in the advanced stage;

• During the study period, voluntarily abide by this trial protocol and receive regular follow-ups;

• All women of childbearing age, fertile men or their spouses who have no plans for fertility or sperm donation throughout the trial period until 6 months after the last dose, or who voluntarily take effective contraceptive measures.

Locations
Other Locations
China
Fudan University Shanghai Cancer Center
RECRUITING
Shanghai
Contact Information
Primary
Jian Zhang, MD,PhD
syner2000@163.com
+8664175590
Time Frame
Start Date: 2024-08-12
Estimated Completion Date: 2027-08-01
Participants
Target number of participants: 100
Treatments
Patients received SG
HER2-negative breast cancer patients who received SG in the advanced stage
Related Therapeutic Areas
Sponsors
Leads: Fudan University

This content was sourced from clinicaltrials.gov

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