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Real-world Effectiveness and Safety Study of Sacituzumab Govitecan in Chinese Metastatic Breast Cancer

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Fudan University

Status

Enrolling

Conditions

Breast Cancer

Treatments

Drug: Sacituzumab Govitecan

Study type

Observational

Funder types

Other

Identifiers

NCT06356519
YOUNGBC-29

Details and patient eligibility

About

The aim of this trial is to explore the real-world effectiveness and poteintial predictors of Sacituzumab Govitecan in Chinese metastatic breast cancer patients.

Enrollment

150 estimated patients

Sex

Female

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients aged over 18 years old.
  2. Metastatic breast cancer included unresectable locally advanced breast cancer, de novo stage IV breast cancer, and recurrent metastatic breast cancer.
  3. Plan to receive or has received Sacituzumab Govitecan monotherapy
  4. Available medical history.

Exclusion criteria

  1. Incomplete medical history.
  2. Pregnancy or breast-breeding

Trial design

150 participants in 1 patient group

Sacituzumab Govitecan
Description:
Sacituzumab Govitecan,10 mg/kg ivgtt d1, d8, q3w
Treatment:
Drug: Sacituzumab Govitecan

Trial contacts and locations

1

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Central trial contact

Biyun Wang, Professor

Data sourced from clinicaltrials.gov

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