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A Clinical Study of SYS6023 Combination Therapy for Advanced Breast Cancer

13. maj 2026 opdateret af: 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.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Detaljeret beskrivelse

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.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

114

Fase

  • Fase 2

Kontakter og lokationer

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

Studiekontakt

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

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:

  • 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.

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: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Cohort 1-Group A
Patients with advanced breast cancer receiving SYS6023 in combination with HB1901 treatment.
SYS6023 er et nyt antistof-lægemiddelkonjugat (ADC), der er rettet mod HER3, administreret via intravenøs infusion.
HB1901 is a specific mTOR inhibitor, administered via intravenous infusion.
Eksperimentel: Cohort 1-Group B
Patients with advanced breast cancer receiving SYS6023 treatment.
SYS6023 er et nyt antistof-lægemiddelkonjugat (ADC), der er rettet mod HER3, administreret via intravenøs infusion.
Eksperimentel: Cohort 2
Patients with advanced breast cancer receiving SYS6023 in combination with KN026 treatment.
SYS6023 er et nyt antistof-lægemiddelkonjugat (ADC), der er rettet mod HER3, administreret via intravenøs infusion.
KN026 is an antibody targeting HER2, administered via intravenous infusion.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Objektiv responsrate (ORR)
Tidsramme: Op til cirka 3 år
Op til cirka 3 år
The incidence of dose-limiting toxicity (DLT)
Tidsramme: 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);
Tidsramme: 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)
Tidsramme: Up to approximately 3 years
Up to approximately 3 years

Sekundære resultatmål

Resultatmål
Tidsramme
Samlet overlevelse (OS)
Tidsramme: Op til cirka 3 år
Op til cirka 3 år
Varighed af svar (DoR)
Tidsramme: Op til cirka 3 år
Op til cirka 3 år
Disease Control Rate (DCR)
Tidsramme: Op til cirka 3 år
Op til cirka 3 år
Progressionsfri-overlevelse (PFS)
Tidsramme: Op til cirka 3 år
Op til cirka 3 år
Maximum Plasma Concentration( Cmax)
Tidsramme: Up to approximately 3 years
Up to approximately 3 years
Time to Maximum Plasma Concentration (Tmax)
Tidsramme: Up to approximately 3 years
Up to approximately 3 years
Area Under the Serum Concentration Time Curve ( AUC)
Tidsramme: Up to approximately 3 years
Up to approximately 3 years
Elimination half-life (t1/2)
Tidsramme: Up to approximately 3 years
Up to approximately 3 years
Anti-Drug Antibody(ADA)
Tidsramme: Up to approximately 3 years
Up to approximately 3 years
Expression level of tumor markers
Tidsramme: Up to approximately 3 years
Up to approximately 3 years
Plasma drug concentration
Tidsramme: Up to approximately 3 years
Up to approximately 3 years

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)

30. maj 2026

Primær færdiggørelse (Anslået)

30. november 2027

Studieafslutning (Anslået)

30. maj 2029

Datoer for studieregistrering

Først indsendt

13. maj 2026

Først indsendt, der opfyldte QC-kriterier

13. maj 2026

Først opslået (Faktiske)

19. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

19. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

13. maj 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • SYS6023-002

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

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Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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