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To evaluate the efficacy and safety of UTD1 in patients with advanced breast cancer.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| UTD1 | UTD1 monotherapy or UTD1 based therapy |
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| Measure | Description | Time Frame |
|---|---|---|
| PFS | Progression free survival | 6 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Adverse events | Number of participants with treatment-related adverse events as assessed by CTCAE v 5.0 | 6 weeks |
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Inclusion Criteria:
Exclusion Criteria:
1.Incomplete medical history.
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Patients diagnosed with breast cancer (according to ICD-10) with confirmed metastasis, regardless of being de novo diagnosed or progressed from a non-metastatic stage
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Fudan University Shanghai Cancer Center | Shanghai | Shanghai Municipality | 200032 | China |
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| ID | Term |
|---|---|
| D001943 | Breast Neoplasms |
| ID | Term |
|---|---|
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D001941 | Breast Diseases |
| D012871 | Skin Diseases |
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| D017437 |
| Skin and Connective Tissue Diseases |