| Eligibility |
Inclusion Criteria:
Subjects will not be included unless they meet all of the following criteria:
1. Males or females age 18 to 75 years old (inclusive) at the time of signing the
informed consent form;
2. Histologically and/or cytologically confirmed TNBC based on pathology reports on
recent biopsy specimens or other pathological samples (central laboratory confirmation
is not required), including:
1. Definition of human epidermal growth factor receptor 2 (HER2) negative:
immunohistochemistry (IHC) of 0 or 1+; if HER is 2+ by IHC, negative HER2
expression must be confirmed by fluorescence in situ hybridization (FISH).
2. Estrogen and progesterone receptor negative means that less than 1% of the cells
express hormone receptors as indicated by IHC;
3. Patients with unresectable locally advanced or metastatic triple-negative breast
cancer who have received at least two lines of standard of care regimens, including:
1. Any treatment received by the patients regardless of triple-negative state can be
included as one of the standard of care regimens;
2. For patients whose treatment regimens have been changed due to intolerability to
toxicity, the intolerable regimens can be included as one of the prior standard
of care regimens;
3. For neoadjuvant and/or adjuvant chemotherapy, if relapse or disease progression
to unresectable locally advanced or metastatic disease occurs during treatment or
within 12 months after discontinuation of treatment (at least 2 cycles have been
completed), it will be considered as one of the standard of care regimens. And
the patients must also have received one therapy and have progressed on this
therapy during the stage of unresectable locally advanced or metastatic disease;
4. For patients with documented germline BRCA1/BRCA2 mutations, if they have been
treated with an approved PARP inhibitor, then the PARP inhibitor can be
considered as one of the 2 prior standard of care regimens required;
5. Patients must have progressed on or were intolerable to the treatment during or
after the last treatment prior to enrollment;
4. All patients must have been previously treated with taxanes; and those who have been
treated with taxanes for at least 1 cycle and show contraindications or intolerability
during or at the end of the cycle can be included, regardless of the disease stage
during this treatment;
5. Patients must have at least one measurable lesion per RECIST v1.1 criteria; those with
only skin or bone lesions cannot be included;
6. Subjects with a Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1
with an expected survival of = 12 weeks;
7. Subjects must provide tumor tissues or tissue specimens;
8. Subjects must have adequate organ and bone marrow function (no blood transfusion,
recombinant human thrombopoietin, or colony stimulating factor therapy has been
received within 2 weeks prior to the screening), which is defined as follows:
1. Hematology: neutrophil count (NEUT) = 1.5 × 109 /L; platelets (PLT) = 100 × 109
/L; hemoglobin = 9 g/dL;
2. Liver function: aspartate aminotransferase (AST), alanine aminotransferase (ALT),
and alkaline phosphatase (ALP) = 2.5 × upper limit of normal (ULN); total
bilirubin (TBIL) = 1.5 × ULN; for patients with liver metastases, ALT and AST
must be = 5 × ULN, TBIL = 2 × ULN; for patients with liver or bone metastases,
ALP must be = 5 × ULN;
3. Albumin = 3 g/dL;
4. Renal function: creatinine clearance (Ccr) = 60 ml/min (see Annex for
Cockcroft-Gault formula);
5. Coagulation function: international normalized ratio (INR), activated partial
thromboplastin time (APTT) and prothrombin time (PT) = 1.5 × ULN;
9. Subjects must have recovered from all toxicities (except alopecia) due to prior
treatments to = grade 1 based on the assessment per CTCAE 5.0 criteria;
10. Subjects voluntarily participate in the study, sign the informed consent form, and
will be able to comply with the protocol-specified visits and relevant procedures.
Exclusion Criteria:
Subjects who meet any of the following criteria will be excluded:
1. Patients with a history of central nervous system (CNS) metastases or current CNS
metastases;
2. Patients with other malignancies, except cured basal or squamous cell skin cancer or
in situ cancer of cervix; and patients with other malignancies must have a tumor-free
period of at least 5 years;
3. Patients with Gilbert's disease;
4. Patients who have received prior TROP2-targeted therapy;
5. Patients who have received live vaccines within 30 days prior to the first dose;
6. Patients who required the treatment of strong inhibitors or inducers of cytochrome
P450 3A4 enzyme (CYP3A4) within 2 weeks prior to the first dose and during the study
treatment (strong inhibitors or inducers of CYP3A4 are not allowed in this study, and
representative drugs of strong CYP3A4 inhibitors or inducers are listed in the Annex).
Patients who received continued high dose of systemic corticosteroids within 2 weeks
prior to the first dose (low-dose corticosteroids, such as = 10 mg daily prednisone or
equivalent, are allowed if the dose is stable for 4 weeks);
7. Patients who have received any chemotherapy, hormonal therapy, radiotherapy,
immunotherapy, biological therapy or other drugs within 4 weeks prior to the first
dose of study treatment or within 5 half-lives of the drug used in the previous period
(whichever is shorter), or received treatment with traditional Chinese medicine
preparations for approved anti-tumor indications 2 weeks prior to the first dose of
study treatment, or received major surgeries 4 weeks prior to the first dose of study
treatment;
8. With concomitant infections requiring systemic antibiotic therapy within 1 week prior
to the first dose of study treatment;
9. Presence of any serious and/or uncontrolled comorbidities that prevent the patient
from participating in the study, such as:
1. Impaired cardiac function, including any of the following: (not necessarily all
of the following):
aa) Corrected QT interval (QTcF) between ventricular depolarization to
repolarization > 480 ms at baseline; ab) Left ventricular ejection fraction
(LVEF) < 50% as indicated by echocardiography (ECHO) ;
2. Other clinically significant heart diseases, including any of the following known
medical history:
ba) Angina pectoris; bb) Congestive cardiac failure; bc) Myocardial infarction;
3. Patients with (noninfectious) interstitial lung disease (ILD) or history of
pneumonia requiring steroid therapy; patients with serious pulmonary function
impairment due to lung disease;
4. Patients with current or previous active chronic inflammatory bowel disease or
intestinal obstruction or gastrointestinal (GI) perforation;
5. Uncontrolled hypertension (systolic blood pressure > 150 mm Hg and/or diastolic
blood pressure > 100 mm Hg), with a history of unstable hypertension, or with a
history of poor compliance with antihypertensive treatment;
6. Uncontrolled diabetes (fasting glucose = 10 mmol/L and/or glycated hemoglobin
(HbA1c) = 8%);
10. Active hepatitis B (hepatitis B surface antigen positive, and HBV-DNA above 500 IU/ml
or 1x ULN, whichever is higher) or hepatitis C (hepatitis C antibody positive, and
HCV-RNA above 1x ULN); with known history of positive human immunodeficiency virus
(HIV) test or known acquired immunodeficiency syndrome (AIDS); positive syphilis
antibody test;
11. History of serious drug allergy, with known allergy to macromolecular protein
preparations or any component of the study drug formulation;
12. Pregnant or lactating women; or patients of childbearing potential (male or female)
who cannot use effective medical contraception during the study treatment period and
for 6 months after the end of the dosing period (see Annex for specific contraceptive
measures);
13. During the screening process prior to the first dose, the condition deteriorated
rapidly, such as severe changes in performance status, unstable pain requiring
adjustment of analgesic therapy;
14. Other circumstances that, in the opinion of the investigator, are not appropriate for
participation in this study.
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