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

3 de septiembre de 2026 actualizado por: 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.

Descripción general del estudio

Estado

Reclutamiento

Condiciones

Tipo de estudio

Intervencionista

Inscripción (Estimado)

216

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana
        • Reclutamiento
        • Peking University First Hospital
        • Contacto:
          • Jianping Li, Doctor of Medicine
          • Número de teléfono: +86 13521531013
          • Correo electrónico: 13521531013@163.com

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador de placebos: Placebo
administrado SC
Experimental: MWX203 monotherapy cohort
This cohort consists of three dose groups: low, medium, and high.
administered subcutaneously (SC)
Experimental: 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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Percentage change in serum TG from baseline at Week 24.
Periodo de tiempo: Baseline, Week 24.
Percentage change in serum TG from baseline at Week 24.
Baseline, Week 24.

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Percentage changes in serum LDL-C from baseline at Week 36
Periodo de tiempo: Baseline, Week 36
Baseline, Week 36
Percentage changes in serum TG from baseline at Week 36
Periodo de tiempo: Baseline, Week 36
Baseline, Week 36
Percentage changes in serum TG from baseline at Weeks 2, 4, 8, 12, 16, 20, 28, 32
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: Baseline, Weeks 24, 36
Baseline, Weeks 24, 36
Incidence of treatment-emergent adverse events (TEAEs)
Periodo de tiempo: 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
Periodo de tiempo: Baseline, Weeks 12, 24, 36
Baseline, Weeks 12, 24, 36

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

25 de septiembre de 2026

Finalización primaria (Estimado)

1 de febrero de 2028

Finalización del estudio (Estimado)

1 de febrero de 2028

Fechas de registro del estudio

Enviado por primera vez

1 de septiembre de 2026

Primero enviado que cumplió con los criterios de control de calidad

1 de septiembre de 2026

Publicado por primera vez (Actual)

4 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

8 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

3 de septiembre de 2026

Última verificación

1 de septiembre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • MWX203-II-DLP

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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