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A Study to Evaluate the Pharmacokinetics, Efficacy, and Safety of HLX319 vs. EU-Phesgo® in the Neoadjuvant Therapy of HER2-Positive Early or Locally Advanced Breast Cancer

15. maj 2026 opdateret af: Shanghai Henlius Biotech

A Multicenter, Randomized, Double-Blind, Parallel-Controlled Phase I Clinical Study to Evaluate the Pharmacokinetics, Efficacy, and Safety of Phesgo® Biosimilar HLX319 vs. EU-Phesgo® in the Neoadjuvant Therapy of HER2-Positive Early or Locally Advanced Breast Cancer

This is a study to compare the similarity in Pharmacokinetics (PK) profile of HLX319 vs. EU-Phesgo® in patients with HER2-positive early or locally advanced breast cancer .

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Detaljeret beskrivelse

This is a randomized, double-blind, parallel-controlled, multi-center Phase I equivalence study to compare the similarity in PK profile of HLX319 vs. EU-Phesgo® in patients with HER2-positive early or locally advanced breast cancer with a primary tumor > 2 cm or nodes-positive.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

258

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Voluntary participation in the clinical study and signed the Informed Consent Form (ICF).
  • Male or female aged ≥ 18 years old at the time of signing the ICF;
  • Histologically confirmed invasive breast cancer, stage II-IIIC, Human Epidermal Growth Factor Receptor 2 (HER2) positive confirmed by central laboratory.
  • Participants agree to undergo surgery while meeting the criteria for surgery after neoadjuvant therapy.
  • Left ventricular ejection fraction (LVEF) at baseline ≥ 55%.
  • An Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-1.
  • Adequate major organ functions.
  • Women with child-bearing potential have a negative result of serum pregnancy test at screening period (within 7 days prior to the first dose) or if they are infertile, non- lactating, reproduction-age men and women following highly effective contraceptive measures until 7 months after last dose.

Exclusion Criteria:

  • Stage IV breast cancer, bilateral breast cancer, or multicentric breast cancer.
  • History of other malignancy within 5 years.
  • Prior systemic therapy for breast cancer treatment or radiotherapy.
  • Patients with a history of ductal carcinoma in situ (DCIS) or lobular carcinoma in situ (LCIS) who have received systemic therapy or radiotherapy to the ipsilateral breast.
  • Patients who have undergone excision biopsy of the primary tumor and/or axillary lymph nodes or lymph node dissection.
  • Have severe heart disease or medical conditions.
  • Participants with viral hepatitis or those with autoimmune hepatitis, sclerosing cholangitis, or liver cirrhosis.
  • Human Immunodeficiency Virus (HIV) infection, HIV antibody positive.
  • Daily use of corticosteroid treatment is required.
  • Sensitivity to any study medications or any of its ingredients or excipients.
  • Participants who underwent any major surgery within 28 days prior to the first dose. Or participants who have received local radiotherapy, radiofrequency ablation, or interventional therapy within 2 weeks prior to the first dose.
  • Received another interventional clinical trial therapy within 4 weeks prior to enrollment in the study, or intentionally participated in another interventional clinical trial during the entire study period.
  • Severe, uncontrolled systemic diseases that may currently interfere with the therapeutic plan.
  • Any other conditions which are inappropriate for the study in the opinion of the investigator.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: HLX319
The regimen in the experimental group is HLX319 in combination with docetaxel and carboplatin.
HLX319 is a biosimilar of pertuzumab-trastuzumab monoclonal antibody injection (subcutaneous injection)
Aktiv komparator: EU-Phesgo®
The regimen in the control group is EU-Phesgo® in combination with docetaxel and carboplatin.
EU-Phesgo® is an original marketed drug product, with the generic name pertuzumab-trastuzumab monoclonal antibody injection (subcutaneous injection)

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Peak concentration (Cmax)
Tidsramme: up to 180 days
Peak concentration after a single drug administration in Cycle 1.
up to 180 days
Area under the serum drug concentration-time curve from 0 to 21 days (AUC0-21d)
Tidsramme: up to 180 days
Area under the serum drug concentration-time curve from 0 to 21 days after a single drug administration in Cycle 1.
up to 180 days
Steady-state peak concentration (Cmax,ss)
Tidsramme: up to 180 days
The steady-state peak concentration after multiple doses administration in Cycle 4.
up to 180 days
Steady-state area under the serum drug concentration-time curve within a dosing interval (AUCss)
Tidsramme: up to 180 days
Steady-state area under the serum drug concentration-time curve within a dosing interval after multiple doses administration in Cycle 4.
up to 180 days

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Trough concentration (Ctrough)
Tidsramme: up to 180 days
Trough concentration after a single dose administration
up to 180 days
Area under the serum drug concentration-time curve from time 0 to infinity (AUC0-inf)
Tidsramme: up to 180 days
Area under the serum drug concentration-time curve from time 0 to infinity after a single dose administration
up to 180 days
Percentage of extrapolated area in the total AUC (%AUCex)
Tidsramme: up to 180 days
Percentage of extrapolated area in the total AUC after a single dose administration
up to 180 days
Time to peak concentration (Tmax)
Tidsramme: up to 180 days
time to peak concentration after a single dose administration
up to 180 days
Elimination half-life (T1/2)
Tidsramme: up to 180 days
elimination half-life after a single dose administration
up to 180 days
Total clearance (CL/F)
Tidsramme: up to 180 days
total clearance after a single dose administration
up to 180 days
Terminal phase distribution volume (Vz/F)
Tidsramme: up to 180 days
terminal phase distribution volume after a single dose administration
up to 180 days
Mean residence time (MRT)
Tidsramme: up to 180 days
mean residence time after a single dose administration
up to 180 days
Steady-state trough concentration (Ctrough,ss)
Tidsramme: up to 180 days
steady-state trough concentration after multiple doses administration in Cycle 4
up to 180 days
Average steady-state concentration (Caverage,ss)
Tidsramme: up to 180 days
average steady-state concentration after multiple doses administration in Cycle 4
up to 180 days
Steady-state time to peak concentration (Tmax,ss)
Tidsramme: up to 180 days
steady-state time to peak concentration after multiple doses administration in Cycle 4
up to 180 days
Elimination half-life (T1/2,ss)
Tidsramme: up to 180 days
elimination half-life after multiple doses administration in Cycle 4
up to 180 days
Steady-state volume of distribution (Vss/F)
Tidsramme: up to 180 days
steady-state volume of distribution after multiple doses administration in Cycle 4
up to 180 days
Steady-state total clearance (CLss/F)
Tidsramme: up to 180 days
steady-state total clearance after multiple doses administration in Cycle 4
up to 180 days
accumulation ratio based on Cmax (RCmax)
Tidsramme: up to 180 days
accumulation ratio based on Cmax after multiple doses administration in Cycle 4
up to 180 days
Accumulation ratio based on AUC (RAUC)
Tidsramme: up to 180 days
accumulation ratio based on AUC after multiple doses administration in Cycle 4
up to 180 days
The total pathological complete response (tpCR) rate assessed by the investigator
Tidsramme: up to 180 days
up to 180 days
Breast pathologic complete response (bpCR) rate assessed by the investigator
Tidsramme: up to 180 days
up to 180 days
Objective response rate (ORR) assessed by the investigator
Tidsramme: up to 180 days
according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 criteria
up to 180 days
Incidence and severity of adverse events (AEs)
Tidsramme: up to 180 days
severity determined according to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version 6.0
up to 180 days
Number of participants with abnormal vital signs
Tidsramme: up to 180 days
Detailed Outcome Measure will be defined in the Statistical Analysis Plan
up to 180 days
Number of participants with abnormal physical examination findings
Tidsramme: up to 180 days
Detailed Outcome Measure will be defined in the Statistical Analysis Plan
up to 180 days
Number of participants with abnormal Laboratory tests results
Tidsramme: up to 180 days
Detailed Outcome Measure will be defined in the Statistical Analysis Plan
up to 180 days
Number of participants with abnormal 12-lead ECG readings
Tidsramme: up to 180 days
Detailed Outcome Measure will be defined in the Statistical Analysis Plan
up to 180 days
Positivity rates of anti-drug antibodies (ADA)
Tidsramme: up to 180 days
up to 180 days
Positivity rates of neutralizing antibodies (NAb)
Tidsramme: up to 180 days
up to 180 days

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

3. juli 2026

Primær færdiggørelse (Anslået)

23. april 2027

Studieafslutning (Anslået)

22. juli 2027

Datoer for studieregistrering

Først indsendt

8. maj 2026

Først indsendt, der opfyldte QC-kriterier

15. maj 2026

Først opslået (Faktiske)

22. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

22. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

15. maj 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • HLX319-BC001

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Kliniske forsøg med HER2 + Brystkræft

Kliniske forsøg med HLX319

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