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Study of Oral HRS-5346 in Adult Patients With Elevated Lipoprotein(a) and High Risk of Cardiovascular Events

12 augustus 2026 bijgewerkt door: Shandong Suncadia Medicine Co., Ltd.

A Randomized, Double-Blind Phase II Study to Evaluate the Efficacy and Safety of Oral HRS-5346 in Adult Patients With Elevated Lipoprotein(a) and High Risk of Cardiovascular Events

This study is designed to evaluate the efficacy and safety of HRS-5346 Tablets in participants with high cardiovascular event risk and elevated Lp(a), and to investigate the appropriate dosage of HRS-5346 Tablets

Studie Overzicht

Toestand

Nog niet aan het werven

Studietype

Ingrijpend

Inschrijving (Geschat)

60

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

Studie Locaties

    • Sichuan
      • Chengdu, Sichuan, China, 610041
        • West China Hospital of Sichuan University
        • Hoofdonderzoeker:
          • Yucheng Chen

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. Understand the specific procedures of the trial, voluntarily participate in this trial, and provide written informed consent;
  2. Aged ≥ 18 years on the day of signing the informed consent form;
  3. Body mass index (BMI) ranging from 18.5 to 40 kg/m²;
  4. High risk of cardiovascular events at screening;
  5. Lp(a) ≥ 150 nmol/L as measured by the central laboratory during the screening period;
  6. For participants receiving pharmacotherapy per clinical practice, they must have been on a stable treatment regimen for a specified duration prior to screening or randomization and are expected to remain on that regimen through the end of the treatment period;
  7. Participants (including their partners) are willing to use effective contraception from the time of signing the informed consent form until 1 month after the last administration of the study drug; female participants must have a negative serum pregnancy test and must not be breastfeeding;
  8. Willing and able to comply with all protocol requirements, including demonstrating adherence to study procedures prior to randomization.

Exclusion Criteria:

  1. Any of the following occurring within 3 months prior to screening, or between screening and randomization: major cardiac or non-cardiac surgery, coronary, carotid or peripheral arterial revascularization, stroke or transient ischaemic attack, myocardial infarction or unstable angina, acute limb ischaemia; as well as arrhythmias requiring treatment but uncontrolled; or other events deemed clinically unstable by the Investigator;
  2. Participants with planned or anticipated cardiac, cerebrovascular, or peripheral arterial surgery, coronary revascularization, or other major surgery during the trial period after randomization;
  3. History of haemorrhagic stroke or other major bleeding, or occurrence of haemorrhagic stroke or other major bleeding events between screening visit and randomization visit;
  4. Participants with an indication for anticoagulation but not receiving anticoagulant therapy at screening;
  5. History of malignancy of any organ system within 5 years prior to screening, or newly diagnosed malignancy of any organ system between screening visit and randomization visit, regardless of signs of local recurrence or metastasis;
  6. Prior history of diseases that significantly affect lipid levels, such as nephrotic syndrome, severe liver disease, Cushing's syndrome, etc.;
  7. Uncontrolled type 1 or type 2 diabetes within 6 months prior to screening, or HbA1c >8.0% at screening (a repeat confirmation is allowed);
  8. History of acute kidney injury within 12 months prior to screening;
  9. Uncontrolled hyperthyroidism or hypothyroidism at screening;
  10. Active infection requiring systemic antiviral or antibacterial medication prior to randomization;
  11. New York Heart Association (NYHA) functional class III-IV heart failure at screening, or the most recently measured left ventricular ejection fraction (LVEF) <30%;
  12. At screening or prior to randomization, participants suffering from major diseases that are unstable and inadequately controlled, in the judgment of the Investigator;
  13. Chronic, continuous, or repeated use of systemic glucocorticoids within 3 months prior to screening;
  14. Receipt of lipoprotein apheresis within 3 months prior to screening, or planned lipoprotein apheresis during the study period;
  15. Prior receipt of specific antisense or gene therapy;
  16. Treatment with oligonucleotides or small interfering ribonucleic acid (siRNA) within 12 months prior to screening;
  17. Use of weight-loss medications resulting in significant weight loss, or surgery leading to substantial weight loss within 3 months prior to screening;
  18. Known hypersensitivity to the active ingredient or any excipient of HRS-5346;
  19. Uncontrolled hypertension prior to randomization;
  20. eGFR < 30 mL/min/1.73 m² at screening or prior to randomization, or participants receiving dialysis;
  21. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), or gamma-glutamyl transferase (GGT) > 2 times the upper limit of normal (ULN), or total bilirubin >1.5 times ULN at screening or prior to randomization;
  22. Human immunodeficiency virus infection (HIV-Ab positive), hepatitis C virus infection (HCV-RNA positive), Treponema pallidum infection (Treponema pallidum antibody positive), hepatitis B virus infection (HBsAg positive) at screening or prior to randomization;
  23. Creatine kinase (CK) > 3 times the upper limit of normal (ULN) prior to randomization;
  24. Thyroid-stimulating hormone (TSH) below the lower limit of normal (LLN) or above the upper limit of normal (ULN) during screening;
  25. Significant abnormal laboratory parameters at screening or prior to randomization that render the participant unsuitable for this study, as judged by the Investigator;
  26. History of drug or alcohol abuse or dependence in the recent past (within 1 year);
  27. Pregnant or breastfeeding women;
  28. Participation in any clinical trial of investigational drug or medical device within 3 months prior to screening, or still within 5 half-lives of the investigational product at screening, whichever is longer;
  29. The Investigator judges that the participant has poor adherence or any other factor rendering participation inappropriate, including but not limited to circumstances where trial participation would expose the participant to unacceptable risk or may confound study results.

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: Verviervoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: Treatment group A: HRS-5346 Dose1
HRS-5346; Dose1
HRS-5346; Dose2
Experimenteel: Treatment group B: HRS-5346 Dose2
HRS-5346; Dose1
HRS-5346; Dose2

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Percentage Change in Lp(a) Levels from Baseline to Week 12
Tijdsspanne: Week 12
Week 12

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Percentage change in Lp(a) levels from baseline to Week 4;
Tijdsspanne: Week 4
Week 4
Absolute change in Lp(a) levels from baseline to Week 4 and Week 12;
Tijdsspanne: Week4, Week 12
Week4, Week 12
Proportion of participants with greater than 70% reduction in Lp(a) levels from baseline at Week 4 and Week 12;
Tijdsspanne: Week4, Week 12
Week4, Week 12
Proportion of participants achieving Lp(a) < 125 nmol/L (i.e., 50 mg/dL) at Week 4 and Week 12;
Tijdsspanne: Week4, Week 12
Week4, Week 12
Proportion of participants achieving Lp(a) < 75 nmol/L (i.e., 30 mg/dL) at Week 4 and Week 12;
Tijdsspanne: Week4, Week 12
Week4, Week 12
Incidence and severity of any adverse event (AE);
Tijdsspanne: Week0- Week 13
Week0- Week 13
Incidence of adverse event of special interest (AESI)
Tijdsspanne: Week0- Week 13
Week0- Week 13
Incidence of serious adverse event (SAE)
Tijdsspanne: Week0- Week 13
Week0- Week 13
Pharmacokinetic assessment: plasma concentrations of HRS-5346.
Tijdsspanne: Week0- Week 13
Week0- Week 13

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)

1 september 2026

Primaire voltooiing (Geschat)

1 februari 2027

Studie voltooiing (Geschat)

1 mei 2027

Studieregistratiedata

Eerst ingediend

12 augustus 2026

Eerst ingediend dat voldeed aan de QC-criteria

12 augustus 2026

Eerst geplaatst (Werkelijk)

17 augustus 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

17 augustus 2026

Laatste update ingediend die voldeed aan QC-criteria

12 augustus 2026

Laatst geverifieerd

1 augustus 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • HRS-5346-202

Plan Individuele Deelnemersgegevens (IPD)

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ONBESLIST

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Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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