Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Phase 2 Clinical Study of MWX203 Injection Alone or in Combination With Inclisiran Sodium Injection in Patients With Mixed Dyslipidemia

3 settembre 2026 aggiornato da: Shanghai Minwei Biotechnology Co., Ltd

A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase 2 Clinical Study to Evaluate the Efficacy and Safety of MWX203 Injection Alone or in Combination With Inclisiran Sodium Injection in Participants With Mixed Dyslipidemia and Inadequate Lipid Control

This is a multicenter, randomized, blinded, placebo-controlled Phase 2 study designed to preliminarily evaluate the efficacy, safety, pharmacokinetic (PK), and immunogenicity profiles of MWX203 Injection alone or in combination with Inclisiran Sodium Injection in participants with mixed dyslipidemia who have inadequate lipid control despite stable statin therapy.

The study includes 5 parallel arms with a planned enrollment of 216 Chinese participants. The study drug is administered subcutaneously once every 12 weeks for a total of 2 doses. The double-blind treatment period lasts 36 weeks, and participants whose lipid levels do not return to baseline will enter a 12-week extended follow-up period. The primary endpoint is the percentage change in serum triglyceride (TG) level from baseline at Week 24.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

216

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Cina
        • Reclutamento
        • Peking University First Hospital
        • Contatto:
          • Jianping Li, Doctor of Medicine
          • Numero di telefono: +86 13521531013
          • Email: 13521531013@163.com

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. Male or female participants aged 18 to 75 years (inclusive) at the time of signing the informed consent form (ICF).
  2. On stable-dose statin therapy (moderate-intensity or above: atorvastatin 10-40 mg, rosuvastatin 5-20 mg, fluvastatin 80 mg, lovastatin 40 mg, pitavastatin 1-4 mg, pravastatin 40 mg, simvastatin 20-40 mg, or Xuezhikang 1.2 g daily) for at least 4 weeks prior to screening, and willing to maintain stable statin use (without changing the type or dose) during the study.
  3. Fasting LDL-C at screening and during run-in meets one of the following criteria (local laboratory): ASCVD very-high risk: LDL-C ≥ 1.4 mmol/L (54 mg/dL); ASCVD high risk: LDL-C ≥ 1.8 mmol/L (70 mg/dL); ASCVD moderate-to-high risk: LDL-C ≥ 2.6 mmol/L (100 mg/dL); ASCVD low risk: LDL-C ≥ 3.4 mmol/L (130 mg/dL).
  4. Fasting TG at screening and during run-in ≥ 1.70 mmol/L (150 mg/dL) and ≤ 5.6 mmol/L (500 mg/dL) (local laboratory).
  5. Participants or their partners have no plans for pregnancy or sperm/egg donation from the time of signing the informed consent form (ICF) until at least 6 months after the last dose and agree to use medically recognized, effective non-pharmacological contraceptive methods throughout the study.
  6. Participants voluntarily agree to participate in the study, are willing to comply with the protocol-required visit schedule and study procedures, and provide written informed consent.

Exclusion Criteria:

  1. Confirmed diagnosis of homozygous familial hypercholesterolemia (HoFH).
  2. History of active pancreatitis within 12 weeks prior to screening.
  3. Severe cardiovascular or cerebrovascular disease within 24 weeks prior to screening or during the run-in period (e.g., hypertensive encephalopathy, transient ischemic attack, severe arrhythmia such as recurrent symptomatic ventricular tachycardia or atrial fibrillation with rapid ventricular rate, or NYHA Class III-IV heart failure); severe aortic/coronary/peripheral vascular disease; or conditions requiring surgical intervention.
  4. Acute ischemic ASCVD event within 48 weeks prior to screening or during the run-in period (e.g., acute coronary syndrome, ischemic stroke); or history of hemorrhagic stroke.
  5. Percutaneous coronary intervention (PCI), coronary artery bypass grafting (CABG), or peripheral arterial revascularization performed within 48 weeks prior to screening, or planned to be performed during the study period.
  6. Uncontrolled hypertension at screening or during run-in: systolic blood pressure (SBP) > 160 mmHg and/or diastolic blood pressure (DBP) > 100 mmHg despite no treatment or at least 4 weeks of stable antihypertensive therapy.
  7. Significant thyroid disease at screening, except for participants receiving stable-dose thyroid hormone replacement or antithyroid therapy for at least 12 weeks prior to screening.
  8. Poorly controlled type 2 diabetes mellitus at screening (HbA1c > 8.5%), or prior diagnosis of type 1 diabetes mellitus.
  9. Serious infection within 4 weeks prior to screening or during run-in, as judged by the investigator to potentially affect protocol compliance or interfere with study results.
  10. Use of any lipid-lowering drug within 4 weeks prior to screening (except for statins administered at a stable dose for at least 4 weeks before screening), or drugs/health products with lipid-regulating effects as judged by the investigator, including but not limited to cholesterol-absorption inhibitors, fibrates, red-yeast-rice-containing products, niacin, omega-3 fatty acids, stanols, or bile-acid sequestrants.
  11. Use of ANGPTL3 inhibitors within 1 year prior to screening.
  12. Use of PCSK9 inhibitors within 180 days prior to screening.
  13. Use of any liver-targeted small nucleic-acid therapeutics within 1 year prior to screening.
  14. Laboratory findings at screening or during run-in meeting any of the following criteria (repeat testing is permitted at screening with documented rationale by the investigator): platelet count ≤ 100 × 10⁹/L; HbA1c > 8.5% (local laboratory); alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2 × ULN; total bilirubin > 1.5 × ULN (> 3 × ULN for participants with a history of Gilbert's syndrome); creatine kinase (CK) > 3 × ULN; TSH below the lower limit of normal (LLN) or > 1.5 × ULN at screening.
  15. Estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 m² at screening or during run-in (calculated using the 2021 CKD-EPI equation).
  16. Left ventricular ejection fraction (LVEF) < 30% on echocardiography at screening.
  17. Body-weight change ≥ 10% (gain or loss) within 3 months prior to screening, or planned weight-loss intervention during the study.
  18. Major lifestyle changes within 4 weeks prior to screening, or inability to comply with dietary control requirements during the study.
  19. Any other condition that, in the investigator's opinion, makes the participant unsuitable for this trial.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore placebo: Placebo
somministrata SC
Sperimentale: MWX203 monotherapy cohort
This cohort consists of three dose groups: low, medium, and high.
administered subcutaneously (SC)
Sperimentale: MWX203 combination-therapy cohort
The MWX203 includes 2 dose levels, whereas inclisiran is administered at a fixed dose.
administered subcutaneously (SC)
284 mg; administered SC

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Percentage change in serum TG from baseline at Week 24.
Lasso di tempo: Baseline, Week 24.
Percentage change in serum TG from baseline at Week 24.
Baseline, Week 24.

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Percentage changes in serum LDL-C from baseline at Week 36
Lasso di tempo: Baseline, Week 36
Baseline, Week 36
Percentage changes in serum TG from baseline at Week 36
Lasso di tempo: Baseline, Week 36
Baseline, Week 36
Percentage changes in serum TG from baseline at Weeks 2, 4, 8, 12, 16, 20, 28, 32
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 28, 32
Baseline, Weeks 2, 4, 8, 12, 16, 20, 28, 32
Percentage changes in serum LDL-C from baseline at Weeks 2, 4, 8, 12, 16, 20, 28, 32
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 28, 32
Baseline, Weeks 2, 4, 8, 12, 16, 20, 28, 32
Percentage changes in serum TC from baseline at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Percentage changes in serum HDL-C from baseline at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Percentage changes in serum non-HDL-C from baseline at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Percentage changes in serum Lp(a) from baseline at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Percentage changes in serum ApoB from baseline at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Percentage changes in serum VLDL-C from baseline at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Percentage changes in serum ApoA1 from baseline at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Percentage changes in serum ApoB/ApoA1 from baseline at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Percentage changes in ANGPTL3 from baseline at Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Lasso di tempo: Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Baseline, Weeks 2, 4, 8, 12, 16, 20, 24, 28, 32, 36
Change in liver fat content measured by MRI-PDFF from baseline at Weeks 24, 36
Lasso di tempo: Baseline, Weeks 24, 36
Baseline, Weeks 24, 36
Incidence of treatment-emergent adverse events (TEAEs)
Lasso di tempo: From First Dose Through End of Study, for at Least 36 Weeks
From First Dose Through End of Study, for at Least 36 Weeks
Assessment of ASCVD Risk Category Using the Pooled Cohort Equations at Weeks 12, 24, and 36
Lasso di tempo: Baseline, Weeks 12, 24, 36
Baseline, Weeks 12, 24, 36

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

25 settembre 2026

Completamento primario (Stimato)

1 febbraio 2028

Completamento dello studio (Stimato)

1 febbraio 2028

Date di iscrizione allo studio

Primo inviato

1 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

1 settembre 2026

Primo Inserito (Effettivo)

4 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

8 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • MWX203-II-DLP

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .