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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. Mai 2026 aktualisiert von: 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 .

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Geschätzt)

258

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

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.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Doppelt

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 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)
Aktiver 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)

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Peak concentration (Cmax)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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

Sekundäre Ergebnismessungen

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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

3. Juli 2026

Primärer Abschluss (Geschätzt)

23. April 2027

Studienabschluss (Geschätzt)

22. Juli 2027

Studienanmeldedaten

Zuerst eingereicht

8. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

15. Mai 2026

Zuerst gepostet (Tatsächlich)

22. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

22. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

15. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • HLX319-BC001

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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