Bioequivalence Study of Paclitaxel Protein-bound Particles for Injectable Suspension (Albumin-bound) in Breast Cancer Patients

NCT07096869 | Recruiting Phase 1

• 1 other identifier: HF112-001
• Study Type: interventional
• Target: 28
• Locations: 1 country
• Sites: 1

Brief Summary

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.

Conditions

Bioequivalence

Outcome Measures

Primary Outcomes (3)

• Peak Plasma Concentration (Cmax)

  Evaluation of Peak Plasma Concentration (Cmax) of total and unbound paclitaxel

  72 hours

• Area under the plasma concentration versus time curve AUC0-t

  Evaluation of Area under the plasma concentration versus time curve AUC0-t of total and unbound paclitaxel

  72 hours

• Area under the plasma concentration versus time curve AUC0-∞

  Evaluation of Area under the plasma concentration versus time curve AUC0-∞ of total and unbound paclitaxel

  72 hours

Secondary Outcomes (3)

• Time to peak Plasma Concentration (Tmax)

  72 hours

• Elimination of half-life (t1/2)

  72 hours

• Incidence of Adverse Events

  Up to 6 mouths

Study Arms (2)

Paclitaxel protein-bound particles for injectable suspension (albumin-bound)

EXPERIMENTAL

The subjects randomly reveived single dose of 260 mg/m\^2 of paclitaxel protein-bound particles for injectable suspension (albumin-bound)

Drug: Paclitaxel protein-bound particles for injectable suspension (albumin-bound)

Abraxane®

EXPERIMENTAL

The subjects randomly reveived single dose of 260 mg/m\^2 of Abraxane®

Drug: Abraxane®

Interventions

Paclitaxel protein-bound particles for injectable suspension (albumin-bound) DRUG

IV infusion, 260 mg/m\^2

Paclitaxel protein-bound particles for injectable suspension (albumin-bound)

Abraxane® DRUG

IV infusion, 260 mg/m\^2

Abraxane®

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• \) 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;
• \) Male and female, ages 18-75 years both inclusive;
• \) 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;
• \) ECOG Score ≤ 2 points;
• \) The expecting life span ≥ 3months;
• \) 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
• \) 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;
• \) Subjects can communicate well with the investigators, understand and comply with the requirements of the study.

You may not qualify if:

• \) A severe allergy or hypersensitivity to paclitaxel or human albumin;
• \) 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;
• \) Those who had undergone major surgery within 4 weeks prior to screening, or planned to undergo major surgery during the study period;
• \) Pregnant or lactating female subjects;
• \) 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;
• \) 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;
• \) Electrocardiogram shows significant abnormality, and/or baseline QTcF interval is \> 470 ms;
• \) Pre-screening sensory neuropathy/peripheral neuropathy are ≥ grade 2;
• \) Blood donation or significant blood loss (\> 400 mL) within 90 days before - screening;
• \) 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.);
• \) 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;
• \) Smoking \> 5 cigarettes per day within 3 months prior to screening or smoking cannot be stopped during the study period;
• \) 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;
• \) 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;
• \) Toxicity caused by using of anti-tumor drugs prior to enrolment do not return to ≤ grade 1 or baseline levels, except for alopecia;

Sponsors & Collaborators

• CSPC Zhongnuo Pharmaceutical (Shijiazhuang) Co., Ltd.: lead

Study Sites (1)

The First Hospital of Jilin University

Changchun, Jilin, 130021, China

RECRUITING

MeSH Terms

Interventions

Albumin-Bound Paclitaxel

Intervention Hierarchy (Ancestors)

Paclitaxel; Taxoids; Cyclodecanes; Cycloparaffins; Hydrocarbons, Alicyclic; Hydrocarbons, Cyclic; Hydrocarbons; Organic Chemicals; Diterpenes; Terpenes; Albumins; Proteins; Amino Acids, Peptides, and Proteins

Central Study Contacts

Clinical Trials Information Group officer

CONTACT

86-0311-69085587; ctr-contact@cspc.cn

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Interventional

Study Record Dates

• First Submitted: July 24, 2025
• First Posted: July 31, 2025
• Study Start: June 26, 2025
• Primary Completion: December 31, 2025
• Study Completion: February 25, 2026
• Last Updated: July 31, 2025

Record last verified: 2025-07

Locations

CN (1)