Overview
The main purpose of this study is to evaluate the bioequivalence of paclitaxel protein-bound particles for injectable suspension (albumin-bound) (100 mg, test product) and Abraxane® (100 mg, reference product) in breast cancer patients.
Eligibility
Inclusion Criteria:
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- Subjects fully understand the purpose, nature, method and possible adverse reactions of the study, volunteer as subjects, and sign informed consent prior to the commencement of any study procedure;
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2) Male and female, ages 18-75 years both inclusive;
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3) Subjects with breast cancer confirmed by histopathology and/or cytology who
meet one of the following conditions: ①Metastatic breast cancer, after failure
of combination chemotherapy for metastatic disease or relapse within 6 months
of adjuvant chemotherapy. Prior therapy should have included an anthracycline
unless clinically contraindicated; ②This treatment criteria (NCCN guidelines
and CSCO guidelines - Breast cancer) is used to determine whether the subjects
are suitable for paclitaxel for injection (albumin-bound) monotherapy.
③Subjects received standard treatment without conditions and were judged to
benefit from injectable paclitaxel (albumin-binding) monotherapy;
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4) ECOG Score ≤ 2 points;
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5) The expecting life span ≥ 3months;
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6) The results of blood, liver and kidney function tests are within the following
ranges: Absolute neutrophil counts (ANC) ≥ 1.5×10^9/L Platelets (PLT) ≥
100×10^9/L Hemoglobin (Hb) ≥ 90 g/L Total bilirubin (TBIL) ≤ 1.5×ULN Alanine
transaminase (ALT), Aspartate aminotransferase (AST)≤×ULN (for patients with
liver metastasis, ≤ 5×ULN) Creatinine clearance (CrCL)≥ 60 mL/min
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7) The subject has no fertility plan (including sperm donation and egg donation)
for at least 6 months from the signing of informed consent to the last dose and
voluntarily takes non-drug effective contraceptive measures;
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8) Subjects can communicate well with the investigators, understand and comply
with the requirements of the study.
Exclusion Criteria:
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- A severe allergy or hypersensitivity to paclitaxel or human albumin;
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2) In addition to cancer, have any other serious liver, kidney/genitourinary,
gastrointestinal (e.g., abdominal inflammation), cardiovascular (e.g.,
congestive heart failure, ventricular arrhythmia, myocardial infarction,
unstable angina), cerebrovascular, pulmonary (e.g., interstitial lung disease),
endocrine, immune, musculoskeletal, neurological, psychiatric, skin, or blood
(e.g., bleeding diathymia or clotting disorders) diseases Patients with a known
or present history of the disease who are deemed unsuitable for enrollment by
the investigators;
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3) Those who had undergone major surgery within 4 weeks prior to screening, or
planned to undergo major surgery during the study period;
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4) Pregnant or lactating female subjects;
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5) Hepatitis B surface antigen positive and HBV DNA positive; HCV core antibody
positive and HCV RNA positive; HIV antigen/antibody positive; treponema
pallidum antibody positive and rapid plasma reaction hormone (RPR) positive;
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6) Those who used chemical small molecule anti-tumor drugs (including endocrine
therapy), biological macromolecular anti-tumor drugs, biological therapy,
radiotherapy or needed to combine other anti-tumor drugs for treatment during
the study period within 4 weeks before the first dose;
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7) Electrocardiogram shows significant abnormality, and/or baseline QTcF interval
is > 470 ms;
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8) Pre-screening sensory neuropathy/peripheral neuropathy are ≥ grade 2;
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9) Blood donation or significant blood loss (> 400 mL) within 90 days before -
screening;
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10) Ingestion of an inhibitor or inducer of CYP2C8 or CYP3A4 within 28 days prior
to dosing (acceptable drug use is stable in homeostasis, that is, the dosing
regimen remains unchanged; However, the use of moderate-strong inhibitory
agents/moderate-strong inducers should be prohibited), or drugs (including
Chinese herbs) that can affect the absorption, distribution, metabolism and
excretion behavior of the study drugs or special diets (such as products
containing caffeine or xanthine, grapefruit fruits and products containing
grapefruit ingredients, etc.);
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11) Those who consumed more than 14 units of alcohol per week in the 3 months
before screening (1 unit ≈ 360 mL for beer, or 45 mL for spirits, or 150 mL for
wine) or who could not stop drinking during the study period or who are
breath-positive for alcohol;
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12) Smoking > 5 cigarettes per day within 3 months prior to screening or smoking
cannot be stopped during the study period;
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13) Any clinically significant abnormal results in the subjects' vital signs,
physical examination, clinical laboratory examination (unless otherwise
specified in the protocol), 12-lead electrocardiogram (ECG) and other
examination results that the investigator deems unsuitable for enrollment;
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14) Within 6 months prior to screening, there is a history of drug abuse (except
regular use of pain medications due to cancer pain) or positive drug abuse
screening;
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15) Toxicity caused by using of anti-tumor drugs prior to enrolment do not return
to ≤ grade 1 or baseline levels, except for alopecia;
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16) Subjects receiving granulocyte-stimulating growth factor treatment within 2
weeks before dosing;
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17) Subjects who have participated in any clinical trial within 1 month before
screening (start from the time of the last dose);
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18) Any other circumstances determined by the investigator to be inappropriate are
not suitable for participation in this study