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- Ensaio Clínico NCT07801820
Phase 2 Clinical Study of MWN109 Tablets in Participants With Type 2 Diabetes Mellitus
A Randomized, Double-Blind, Placebo- and Active-Controlled, Multicenter Phase II Clinical Trial to Evaluate the Efficacy, Safety, and Pharmacokinetic Characteristics of MWN109 Tablets in Participants With Type 2 Diabetes Mellitus
This is a randomized, double-blind, placebo- and active-controlled, multicenter Phase II clinical trial designed to evaluate the efficacy, safety, and pharmacokinetic characteristics of MWN109 tablets in participants with type 2 diabetes mellitus (T2DM).
Eligible participants will be randomized to receive different dose levels of MWN109 tablets, MWN109-matched placebo, or semaglutide tablets 14 mg (active control), administered once daily for 20 consecutive weeks.
Approximately 240 adults aged 18 to 75 years with type 2 diabetes mellitus will be enrolled. The primary endpoint is the percent change from baseline in HbA1c at Week 20. Secondary endpoints include glycemic parameters, body weight, metabolic parameters, adverse events, and immunogenicity.
Visão geral do estudo
Status
Condições
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 2
Contactos e Locais
Contato de estudo
- Nome: Wanxiang Chen
- Número de telefone: +86 13359015677
- E-mail: chenwanxiang@minweibiotech.com
Locais de estudo
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Beijing Municipality
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Beijing, Beijing Municipality, China
- Recrutamento
- Peking University People's Hospital
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Contato:
- Linong Ji, Doctor
- Número de telefone: +86 10 88324100
- E-mail: jiln@bjmu.edu.cn
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-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Male or female participants aged 18 to 75 years (inclusive) at the time of signing the informed consent form.
- Diagnosis of type 2 diabetes mellitus for at least 3 months prior to screening, with inadequate glycemic control despite treatment with lifestyle intervention or a stable dose of metformin monotherapy (≥1500 mg/day, or ≥1000 mg/day if at the maximum tolerated dose) for at least 3 months prior to screening.
- HbA1c ≥7.5% and ≤11.0% at screening and before randomization (central laboratory).
- Fasting plasma glucose ≤13.9 mmol/L at screening and before randomization (central laboratory; may be re-tested once within 1 week if special circumstances apply).
- BMI ≥20.0 kg/m² and ≤40.0 kg/m² at screening.
- Self-reported body weight change of <5% during the at least 12 weeks prior to screening.
Exclusion Criteria:
- Known allergic constitution (allergy to 3 or more foods or drugs), allergy to GLP-1 receptor agonists or any component of the study drug, severe allergic disease, or a history of severe drug allergy.
- Diagnosed or suspected type 1 diabetes mellitus, other specific types of diabetes mellitus (excluding gestational diabetes mellitus), or secondary diabetes mellitus.
- Severe chronic complications of diabetes mellitus (e.g., diabetic nephropathy, proliferative diabetic retinopathy, non-proliferative diabetic retinopathy requiring treatment, peripheral vascular disease with amputation, chronic foot ulcer, intermittent claudication, or painful diabetic neuropathy).
- Use of insulin within 1 year prior to randomization (except for acute short-term use of ≤14 days).
- Diabetic ketoacidosis or hyperosmolar hyperglycemic state within 24 weeks prior to randomization.
- Grade 3 hypoglycemia within 12 months prior to randomization, or ≥3 episodes of Grade 2 hypoglycemia or hypoglycemia-related symptoms within 3 months prior to screening.
- Trauma, infection, or surgery within 12 weeks prior to randomization that significantly affects glycemic control, or planned surgery during the study period (excluding outpatient procedures).
- Blood transfusion or blood donation/blood loss ≥400 mL within 12 weeks prior to randomization, or ≥200 mL within 4 weeks prior to screening, or hematologic diseases that may affect HbA1c or pose a safety risk.
- Any unstable or untreated endocrine disease other than type 2 diabetes mellitus (e.g., multiple endocrine neoplasia, acromegaly, Cushing's syndrome).
- History of thyroid disease (except under specific circumstances) or abnormal TSH (TSH >6.0 or <0.4 mIU/L in participants without a history of thyroid disease).
- Medullary thyroid carcinoma, multiple endocrine neoplasia type 2 (MEN2), or a personal or first-degree family history of these conditions.
- Significant active autoimmune abnormalities (e.g., systemic lupus erythematosus, rheumatoid arthritis) requiring systemic glucocorticoids.
- Major cardiovascular or cerebrovascular diseases within 24 weeks prior to screening or before randomization (e.g., myocardial infarction, cerebrovascular accident, unstable angina).
- Known or pre-randomization ECG abnormalities with significant safety risk (e.g., QTcF >450 ms).
- History of sporadic or frequent premature beats or tachycardia, or heart rate >100 beats/min before randomization.
- Uncontrolled hypertension at screening or before randomization (≥160/100 mmHg) or untreated hypertension meeting this criterion.
- Clinically significant abnormal laboratory findings at screening or before randomization (e.g., ALT or AST ≥3×ULN, eGFR <60 mL/min/1.73 m², anemia, calcitonin ≥35 ng/L).
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Dobro
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Comparador de Placebo: Placebo
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Administered orally, QD, 20 weeks
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Experimental: MWN109 Cohort 1
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Administered orally, QD, 20 weeks
|
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Experimental: MWN109 Cohort 2
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Administered orally, QD, 20 weeks
|
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Experimental: MWN109 Cohort 3
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Administered orally, QD, 20 weeks
|
|
Experimental: MWN109 Cohort 4
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Administered orally, QD, 20 weeks
|
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Comparador Ativo: Semaglutide Tablets
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Administered orally, QD, 20 weeks
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Change in Glycated Hemoglobin (HbA1c) from Baseline at Week 20 Compared to Placebo
Prazo: Baseline, Week 20
|
HbA1c is the glycated fraction of hemoglobin A. HbA1c is measured to identify the average plasma glucose concentration over prolonged periods.
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Baseline, Week 20
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Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
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Change in HbA1c from Baseline at Week 20 Compared with Semaglutide Tablets
Prazo: Baseline, Week 20
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Baseline, Week 20
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Change from baseline in HbA1c
Prazo: Baseline, Week 4, Week 8, Week 12, Week 16
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Baseline, Week 4, Week 8, Week 12, Week 16
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Percentage of Participants With an HbA1c target value of < 7.0%
Prazo: Week 4, Week 8, Week 12, Week 16
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Week 4, Week 8, Week 12, Week 16
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Percentage of Participants With an HbA1c target value of ≤ 6.5%
Prazo: Week 4, Week 8, Week 12, Week 16
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Week 4, Week 8, Week 12, Week 16
|
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Percentage of Participants With an HbA1c target value of ≤ 5.7%
Prazo: Week 4, Week 8, Week 12, Week 16]
|
Week 4, Week 8, Week 12, Week 16]
|
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Percentage of Participants With an HbA1c target value of ≤6.5% Without Confirmed Symptomatic Hypoglycemia
Prazo: Week 20
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Week 20
|
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Percentage of Participants With an HbA1c target value of ≤6.5% and ≥10% Body Weight Reduction
Prazo: Week 20
|
Week 20
|
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Percentage of Participants With an HbA1c target value of <7.0% Without Confirmed Symptomatic Hypoglycemia
Prazo: Week 20
|
Week 20
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- MWN109-Oral-T2DM-II
Plano para dados de participantes individuais (IPD)
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Informações sobre medicamentos e dispositivos, documentos de estudo
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