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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 mei 2026 bijgewerkt door: 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 .

Studie Overzicht

Toestand

Nog niet aan het werven

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Geschat)

258

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Dubbele

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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)
Actieve vergelijker: 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)

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Peak concentration (Cmax)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Trough concentration (Ctrough)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: up to 180 days
time to peak concentration after a single dose administration
up to 180 days
Elimination half-life (T1/2)
Tijdsspanne: up to 180 days
elimination half-life after a single dose administration
up to 180 days
Total clearance (CL/F)
Tijdsspanne: up to 180 days
total clearance after a single dose administration
up to 180 days
Terminal phase distribution volume (Vz/F)
Tijdsspanne: up to 180 days
terminal phase distribution volume after a single dose administration
up to 180 days
Mean residence time (MRT)
Tijdsspanne: up to 180 days
mean residence time after a single dose administration
up to 180 days
Steady-state trough concentration (Ctrough,ss)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: up to 180 days
up to 180 days
Breast pathologic complete response (bpCR) rate assessed by the investigator
Tijdsspanne: up to 180 days
up to 180 days
Objective response rate (ORR) assessed by the investigator
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: up to 180 days
up to 180 days
Positivity rates of neutralizing antibodies (NAb)
Tijdsspanne: up to 180 days
up to 180 days

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

3 juli 2026

Primaire voltooiing (Geschat)

23 april 2027

Studie voltooiing (Geschat)

22 juli 2027

Studieregistratiedata

Eerst ingediend

8 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

15 mei 2026

Eerst geplaatst (Werkelijk)

22 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

22 mei 2026

Laatste update ingediend die voldeed aan QC-criteria

15 mei 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • HLX319-BC001

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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