| Eligibility |
Inclusion Criteria:
- The subject can understand the informed consent, voluntarily participate and sign the
informed consent ;
- Subjects are older than or equal to 18 years old and younger than or equal to 75 years
old on the day of signing the informed consent;
- Histologically or cytologically confirmed, metastatic or locally advanced unresectable
HER2-positive solid tumors;
- Prior antitumor therapy needs to meet the following conditions:
Her2-positive GC/GEJ: has not received prior systemic treatment for metastatic or locally
advanced unresectable GC/GEJ, or has received prior systemic treatment=1 line of systemic
treatment with disease progression, front-line systemic treatment includes at least
platinum or fluorouracil based chemotherapy with or without trastuzumab; Subjects who
relapsed within 6 months after the end of neoadjuvant/adjuvant chemotherapy were considered
as line 1 treatment failure; Her2-positive BC: prior treatment with =1 line of
HER2-targeted therapy for metastatic disease and disease progression; Subjects who relapsed
within 12 months after the end of neoadjuvant/adjuvant chemotherapy were considered as line
1 treatment failure; Other HER2-positive solid tumors: previous =1 line of systemic therapy
for metastatic or locally advanced unresectable tumors with disease progression, no clear
standard therapy for prolongation of survival, or after subjects rejected 1 line of
systemic therapy; Frontline systemic therapy for ovarian and cervical cancer includes at
least platinum-based (cisplatin or carboplatin) chemotherapy; Frontline systemic therapy
for ESCC and mCRC includes at least platinum combined with fluorouracil or tax-based
chemotherapy; MCRC requires =2 lines of systemic therapy for metastatic or locally advanced
unresectable tumors and disease progression; Subjects who relapsed within 6 months after
completion of neoadjuvant/adjuvant platinum-containing chemotherapy Line 1 treatment
failure;
- At least 1 measurable lesion at baseline according to RECIST1.1 criteria;
- ECOG score 0 or 1;
- Left ventricular ejection fraction (LVEF) = 50% at baseline as determined by either
ECHO (preferred) or MUGA;
- Liver function met the following criteria within 7 days prior to initial
administration:
Total bilirubin =1.0x ULN (Gilbert's syndrome, or total bilirubin =1.5x ULN in liver
metastases); Aminotransferase (ALT/AST) =1.5x ULN (liver metastatic subjects =3xULN);
-Renal function within 7 days prior to initial administration: serum creatinine =1.5x ULN
and serum creatinine clearance =60mL/min (according to Cockcroft-Gault Formula
calculation);
-Bone marrow function met the following criteria within 7 days prior to initial
administration: Hemoglobin =90 g/L; Neutrophil absolute count =1.5 x 109/L; Platelet count
=100x 109/L; INR or PT=1.5x ULN, and aPTT= 1.5x ULN;
- TSH normal range: If TSH is abnormal, total or free T3 and free T4 should be in the
normal range
- Life expectancy >3 months;
- Fertile female subjects or fertile male subjects with a partner agreed to use hepa
beginning 7 days prior to the first dose pregnancy continued until 24 weeks after drug
withdrawal. Fertile female subjects must have a negative serum pregnancy test within 7
days prior to first dosing;
- The subjects are able and willing to follow the visits, treatment plans, laboratory
tests, and other study-related procedures specified in the study protocol
Exclusion Criteria:
- Untreated active brain metastasis or leptomeningeal metastasis;
- Historyof Left ventricular ejection fraction (LVEF) decline to < 45% or absolute
decrease for > 15% during the treatment course from prior HER2-targeted therapy;
- Previous cumulative doses of anthracycline exceeded doxorubicin or liposomal
doxorubicin >320mg/m2 or equivalent doses of other anthracyclines;
- Has received other anti-tumor treatment or an investigational drug within 28 days or 5
half-lives prior(whichever is shorter, but at least 2 weeks) to the first trial
treatment;
- Major surgery (transabdominal, transthoracic, etc.) within 28 days prior to initial
administration; Diagnostic puncture or peripheral vascular is not included pathway
replacement)
- Radical radiotherapy within 3 months prior to initial administration; Palliative
radiotherapy is allowed 2 weeks before administration, and the dose of radiotherapy is
in line with local palliative the diagnosis and treatment standard of sexual therapy
and the coverage of radiotherapy is less than 30% of the bone marrow region;
- Prior treatment with immune checkpoint blockers or T cell costimulators;
- Systemic corticosteroid or immunosuppressant therapy is required for 7 consecutive
days within 14 days of initial dosing
- Received live vaccines (including attenuated live vaccines) within 28 days of initial
administration;
- Have interstitial lung disease or a history of non-infectious pneumonia requiring oral
or intravenous glucocorticoid treatment;
- Have a past or current autoimmune disease;
- Other malignant tumors occurred within 5 years prior to initial administration;
- With uncontrolled comorbidities;
- Toxicity from previous antitumor therapy did not return to CTCAE grade =1 (NCI-CTCAEV
5.0) or baseline levels;
- Prior allo-HSCT or solid organ transplant;
- History of allergic reaction, hypersensitivity reaction and intolerance to antibody
drugs; Prior allergic reaction to medication ;
- Pregnant or nursing females;
- Other medical conditions that at the discretion of investigator interfere with the
requirements of the trial in terms of safety or efficacy evaluation, or treatment
compliance;
- BMI less than 18.5kg/m2 or weight loss =10% within 2 months prior to screening.
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