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A Clinical Study of SYS6023 Combination Therapy for Advanced Breast Cancer

15 juni 2026 bijgewerkt door: 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.

Studie Overzicht

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Geschat)

36

Fase

  • Fase 2

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

  • Naam: Clinical Trials Information Group Officer
  • Telefoonnummer: 86-0311-69085587
  • E-mail: ctr-contact@cspc.cn

Studie Contact Back-up

Studie Locaties

    • Heilonjiang
      • Harbin, Heilonjiang, China, 150000
        • Werving
        • Affiliated Tumor Hospital of Harbin
        • Contact:

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:

  • 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.

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: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: SYS6023 in combination with KN026
Patients with advanced breast cancer receiving SYS6023 in combination with KN026 treatment.
SYS6023 is een nieuw antilichaam-medicijnconjugaat (ADC) gericht op HER3, toegediend via intraveneuze infusie.
KN026 is an antibody targeting HER2, administered via intravenous infusion.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Objectief responspercentage (ORR)
Tijdsspanne: Tot ongeveer 3 jaar
Tot ongeveer 3 jaar
The incidence of dose-limiting toxicity (DLT)
Tijdsspanne: 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);
Tijdsspanne: 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)
Tijdsspanne: Up to approximately 3 years
Up to approximately 3 years

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Algehele overleving (OS)
Tijdsspanne: Tot ongeveer 3 jaar
Tot ongeveer 3 jaar
Duur van de respons (DoR)
Tijdsspanne: Tot ongeveer 3 jaar
Tot ongeveer 3 jaar
Ziektecontrolepercentage (DCR)
Tijdsspanne: Tot ongeveer 3 jaar
Tot ongeveer 3 jaar
Progressievrije overleving (PFS)
Tijdsspanne: Tot ongeveer 3 jaar
Tot ongeveer 3 jaar
Maximum Plasma Concentration( Cmax)
Tijdsspanne: Up to approximately 3 years
Up to approximately 3 years
Time to Maximum Plasma Concentration (Tmax)
Tijdsspanne: Up to approximately 3 years
Up to approximately 3 years
Area Under the Serum Concentration Time Curve ( AUC)
Tijdsspanne: Up to approximately 3 years
Up to approximately 3 years
Elimination half-life (t1/2)
Tijdsspanne: Up to approximately 3 years
Up to approximately 3 years
Anti-Drug Antibody(ADA)
Tijdsspanne: Up to approximately 3 years
Up to approximately 3 years
Expression level of tumor markers
Tijdsspanne: Up to approximately 3 years
Up to approximately 3 years
Plasma drug concentration
Tijdsspanne: Up to approximately 3 years
Up to approximately 3 years

Medewerkers en onderzoekers

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

Onderzoekers

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

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 (Werkelijk)

25 mei 2026

Primaire voltooiing (Geschat)

30 november 2027

Studie voltooiing (Geschat)

30 mei 2029

Studieregistratiedata

Eerst ingediend

13 mei 2026

Eerst ingediend dat voldeed aan de QC-criteria

13 mei 2026

Eerst geplaatst (Werkelijk)

19 mei 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

16 juni 2026

Laatste update ingediend die voldeed aan QC-criteria

15 juni 2026

Laatst geverifieerd

1 mei 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • SYS6023-002

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

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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