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A Clinical Study of SYS6023 Combination Therapy for Advanced Breast Cancer

15. Juni 2026 aktualisiert von: CSPC Megalith Biopharmaceutical Co.,Ltd.

A Phase II Clinical Study Evaluating the Efficacy and Safety of SYS6023 Combination Therapy for Unresectable Locally Advanced or Metastatic Breast Cancer

This is an open-label, multicenter Phase II clinical study conducted in subjects with advanced breast cancer.

Studienübersicht

Status

Rekrutierung

Detaillierte Beschreibung

This is an open-label, multicenter Phase II clinical study conducted in subjects with advanced breast cancer.

The study aims to evaluate the safety/tolerability, pharmacokinetics, and preliminary efficacy of SYS6023 in combination with other agents in subjects with advanced breast cancer.

Eligible subjects will receive SYS6023 in combination with HB1901 or KN026, with each treatment cycle lasting 3 weeks, until disease progression, intolerable toxicity, initiation of new anti-tumor therapy, withdrawal of informed consent, loss to follow-up, or death, whichever occurs first.

Studientyp

Interventionell

Einschreibung (Geschätzt)

36

Phase

  • Phase 2

Kontakte und Standorte

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

Studienkontakt

  • Name: Clinical Trials Information Group officer
  • Telefonnummer: 86-0311-69085587
  • E-Mail: ctr-contact@cspc.cn

Studieren Sie die Kontaktsicherung

Studienorte

    • Heilonjiang
      • Harbin, Heilonjiang, China, 150000
        • Rekrutierung
        • Affiliated Tumor Hospital of Harbin
        • Kontakt:

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:

  • 1. Age ≥ 18 years old;
  • 2. Histologically or cytologically confirmed unresectable locally advanced or metastatic breast cancer:
  • 3. Sufficient tumor specimens must be provided for biomarker testing (human epidermal growth factor receptor 3-HER3), preferably obtained during or after the most recent treatment period; During safety run-in period, subjects who cannot provide sufficient tissue samples may be screened after sponsor's evaluation and approval;
  • 4. Documented disease progression or intolerability with the most recent systemic anti-tumor treatment;
  • 5. According to RECIST 1.1, at least one evaluable lesion (safety run-in period) or measurable lesion (cohort expansion phase);
  • 6. ECOG PS score 0-1;
  • 7. Expected survival ≥ 3 months;
  • 8. Adequate organ function with laboratory tests meeting criteria (no blood transfusion or hematopoietic growth factor therapy within 14 days before testing): ANC ≥ 1.5 × 10^9/L PLT ≥ 100 × 10^9/L Hb ≥ 90 g/L TBIL ≤ 1.5 × ULN ALT, AST ≤ 2.5 × ULN; for participants with liver metastasis, ALT and AST ≤ 5 × ULN Creatinine clearance rate (Ccr) > 35 mL/min (calculated according to Cockcroft-Gault formula) Activated partial thromboplastin time (APTT) ≤ 1.5 × ULN; International normalized ratio (INR) ≤ 1.5 × ULN Left ventricular ejection fraction (LVEF) ≥ 55% (only applicable to Cohort 2)
  • 9. Eligible individuals with reproductive potential must agree to use reliable contraceptive methods (hormonal contraceptives, barrier methods, or abstinence) with their partners during the trial and for at least 7 months after the last dose; Women of childbearing potential must have a negative blood pregnancy test within 7 days before enrollment;
  • 10. Fully understand this clinical trial and voluntarily sign the written informed consent form.

Exclusion Criteria:

  • 1. Prior treatment with HER3-targeted ADC therapy;
  • 2. Applicable to Cohort 1: a. Prior treatment with any topoisomerase I inhibitor-loaded ADC therapy; b. Current presence or impending visceral crisis that has caused or may cause impending organ damage and/or other life-threatening complications;
  • 3. Applicable to Cohort 2: a. Prior exposure to anthracyclines with cumulative dose exceeding 360 mg/m^2doxorubicin equivalent; b. LVEF once dropped to < 40% during prior anti-HER2 drug therapy, or symptomatic CHF occurred;
  • 4. History of other malignancies within 3 years before randomization/first dose or concurrent active malignancies (except cured localized tumors such as basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, carcinoma in situ of the prostate, carcinoma in situ of the cervix, carcinoma in situ of the breast, etc., which are allowed to enroll);
  • 5. Untreated (including those detected during screening period) or unstable brain parenchymal metastasis, spinal cord metastasis or compression, carcinomatous meningitis. Subjects with treated stable brain metastases may be considered for enrollment (Note: refers to participants who have received local brain treatment, whose symptoms are stable, imaging tests show stability for at least 28 days before randomization/first dose, no evidence of progressive brain edema, and no need for glucocorticoids or other symptom control measures);
  • 6. Adverse reactions from prior anti-tumor therapy have not recovered to CTCAE 6.0 grade ≤ 1 (except for toxicities such as alopecia that researchers judge to have no safety risk);
  • 7. Major surgery within 28 days before randomization/first dose, or planned to undergo systemic or local tumor resection during the study period;
  • 8. History of severe bleeding risk (e.g., gastrointestinal varices) or bleeding diathesis, any gastrointestinal bleeding or other bleeding of ≥ CTCAE grade 2 within 28 days before randomization/first dose; Abdominal fistula, gastrointestinal perforation or abdominal abscess within 6 months before randomization/first dose;
  • 9. History of severe cardiovascular disease, including but not limited to:

    1. Acute coronary syndrome within 6 months before randomization/first dose;
    2. Stroke or transient ischemic attack within 6 months before randomization/first dose;
    3. Pulmonary embolism or deep vein thrombosis within 3 months before randomization/first dose (intermuscular vein thrombosis may be enrolled if assessed as low risk by researchers);
    4. CHF with NYHA functional classification ≥ II;
    5. Documented history of cardiomyopathy that has not currently recovered;
    6. Pericarditis;
    7. Severe arrhythmia, such as ventricular arrhythmia requiring clinical intervention, II-III degree atrioventricular block, etc.;
    8. Baseline average QTcF > 450 ms (calculated using Fridericia formula), or history or family history of long QT syndrome;
    9. Uncontrolled hypertension (defined as persistent systolic blood pressure ≥ 150 mmHg and/or diastolic blood pressure ≥ 100 mmHg despite antihypertensive medication);
  • 10. Presence of non-infectious lung disease/pneumonia requiring treatment at randomization/first dose, or history of interstitial lung disease/pneumonia requiring glucocorticoid treatment during prior anti-tumor therapy;
  • 11. Active bacterial, fungal or viral infection within 14 days before randomization/first dose (defined as requiring intravenous anti-bacterial, anti-fungal or anti-viral drug therapy). Individuals receiving prophylactic anti-infective therapy without clinical manifestations of active infection may be considered for enrollment;
  • 12. Active hepatitis B or hepatitis C, defined as HBsAg positive and HBV DNA > 2000 IU/mL for active hepatitis B; defined as HCV-Ab positive and HCV RNA > ULN for active hepatitis C;
  • 13. History of immunodeficiency or positive HIV antibody test during screening;
  • 14. Use of strong CYP3A4 inducers or inhibitors, OATP1B1 or OATP1B3 inhibitors before randomization/first dose (within 5 half-lives of inducer or inhibitor) or need to use such drugs during study treatment;
  • 15. Known or suspected hypersensitivity to the study drug or its components;
  • 16. Lactating women;
  • 17. Presence of other conditions that may interfere with participants' participation in study procedures, not in line with participants' maximum benefit from participating in the study, or affect study results: such as history of mental illness, drug abuse or substance abuse, any other clinically significant disease or condition, etc.

Studienplan

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

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: N / A
  • Interventionsmodell: Einzelgruppenzuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: SYS6023 in combination with KN026
Patients with advanced breast cancer receiving SYS6023 in combination with KN026 treatment.
SYS6023 ist ein neuartiges Antikörper-Drogen-Konjugat (ADC), das HER3 abzielt und über intravenöse Infusion verabreicht wird.
KN026 is an antibody targeting HER2, administered via intravenous infusion.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Objektive Ansprechrate (ORR)
Zeitfenster: Bis ca. 3 Jahre
Bis ca. 3 Jahre
The incidence of dose-limiting toxicity (DLT)
Zeitfenster: At the end of Cycle 1 (each cycle is 21 days).
At the end of Cycle 1 (each cycle is 21 days).
Frequency and severity of AEs and SAEs (according to NCI-CTCAE 6.0);
Zeitfenster: Baseline up to 28 days post last dose, Up to approximately 3 years
Baseline up to 28 days post last dose, Up to approximately 3 years
Recommended Phase 2 Dose(RP2D)
Zeitfenster: Up to approximately 3 years
Up to approximately 3 years

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Gesamtüberleben (OS)
Zeitfenster: Bis ca. 3 Jahre
Bis ca. 3 Jahre
Dauer der Reaktion (DoR)
Zeitfenster: Bis ca. 3 Jahre
Bis ca. 3 Jahre
Krankheitskontrollrate (DCR)
Zeitfenster: Bis ca. 3 Jahre
Bis ca. 3 Jahre
Progressionsfreies Überleben (PFS)
Zeitfenster: Bis ca. 3 Jahre
Bis ca. 3 Jahre
Maximum Plasma Concentration( Cmax)
Zeitfenster: Up to approximately 3 years
Up to approximately 3 years
Time to Maximum Plasma Concentration (Tmax)
Zeitfenster: Up to approximately 3 years
Up to approximately 3 years
Area Under the Serum Concentration Time Curve ( AUC)
Zeitfenster: Up to approximately 3 years
Up to approximately 3 years
Elimination half-life (t1/2)
Zeitfenster: Up to approximately 3 years
Up to approximately 3 years
Anti-Drug Antibody(ADA)
Zeitfenster: Up to approximately 3 years
Up to approximately 3 years
Expression level of tumor markers
Zeitfenster: Up to approximately 3 years
Up to approximately 3 years
Plasma drug concentration
Zeitfenster: Up to approximately 3 years
Up to approximately 3 years

Mitarbeiter und Ermittler

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

Ermittler

  • Hauptermittler: Qingyuan Zhang, M.D., Affiliated Tumor Hospital of Harbin

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 (Tatsächlich)

25. Mai 2026

Primärer Abschluss (Geschätzt)

30. November 2027

Studienabschluss (Geschätzt)

30. Mai 2029

Studienanmeldedaten

Zuerst eingereicht

13. Mai 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

13. Mai 2026

Zuerst gepostet (Tatsächlich)

19. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

16. Juni 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

15. Juni 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • SYS6023-002

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

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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