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A Phase 2 Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of SAL0150 Tablets in Subjects With Type 2 Diabetes Mellitus

2 de novembro de 2026 atualizado por: Shenzhen Salubris Pharmaceuticals Co., Ltd.

A Phase 2, Multicenter, Randomized, Double-blind, Placebo and Active Comparator-controlled, Parallel-Group Study to Evaluate the Efficacy, Safety, and Pharmacokinetics Characteristics of SAL0150 Tablets in Subjects With Type 2 Diabetes Mellitus Inadequate Glycemic Control

This study is a multicenter, randomized, double-blind (with open-lable semaglutide 1.0 mg, active comparator), placebo-and active-controlled, parallel-group Phase 2 clinical trial aimed at evaluating the efficacy, safety and pharmacokinetic (PK) characteristics of SAL0150 tablets in subjects with Type 2 Diabetes Mellitus (T2DM) who have inadequate glycemic control after diet and exercise alone or after diet and exercise combined with stable-dose metformin monotherapy.

Visão geral do estudo

Descrição detalhada

This phase 2, multicenter, randomized, double-blind, placebo-and active-controlled, parallel-group study aims to assess the efficacy, safety and PK characteristics of SAL0150 tablets in adult participants with T2DM inadequately controlled with diet and exercise alone or after diet and exercise combined with stable-dose metformin monotherapy.

The study includes a screening period of approximately 2 weeks, a run-in period of 3 weeks or 6 weeks (placebo, or placebo combined with stable-dose Glucophage XR), a 15-week treatment period, and a 2-week follow-up period, for a total duration of approximately 23 or 26 weeks.

A total of 364 participants will be randomized in this study, and will be stratified according to baseline glycated hemoglobin (HbA1c) (≤ 8.5% or > 8.5%) and background diabetes treatment (diet and exercise alone, or diet and exercise combined with metformin monotherapy). Eligible participants will be randomized 1:1:1:1:1:1:1 to receive different doses of SAL0150, placebo, or open-label semaglutide 1.0 mg (active comparator), with 52 subjects in each treatment group.The primary endpoint is the change from baseline in HbA1c at Week 16.

Tipo de estudo

Intervencional

Inscrição (Estimado)

364

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

  • Nome: Linong Ji, M.D
  • Número de telefone: 0086108832451 00861088325578
  • E-mail: jiln@bjmu.edu.cn

Locais de estudo

    • Beijing Municipality
      • Beijing, Beijing Municipality, China
        • Peking University People's Hospital
        • Contato:
          • Linong Ji, M.D
          • Número de telefone: 0086108832451 00861088325578
          • E-mail: jiln@bjmu.edu.cn

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Male or female, age above or equal to 18 years at the time of signing informed consent;

  • Diagnosed with type 2 diabetes mellitus according to the World Health Organization (WHO) diagnostic criteria for diabetes (2011) and classification criteria, and with a disease duration of at least 3 months at screening;

  • Participants who had received any of the following glycemic control regimens prior to screening and had inadequate glycemic control:

    • Diet and exercise intervention alone for at least 8 weeks;
    • Diet and exercise intervention combined with monotherapy with a stable dose of metformin (daily dose ≥ 1000 mg) for at least 6 weeks;
  • HbA1c ≥7.5% and ≤11.0% at screening as assessed by the local laboratory;

  • Body mass index (BMI) ≥20.0 kg/m2 and ≤42.0 kg/m2 at screening/randomization;

  • No significant change in body weight within 3 months prior to screening (weight gain or loss < 5%);

  • Able to understand the procedures and methods of this study, willing to strictly follow the clinical trial protocol to complete this trial, and voluntarily sign the informed consent form.

Exclusion Criteria:

  • Any of the following endocrine-related medical histories or evidence prior to screening:

    1. Diagnosis or suspected type 1 diabetes, special types of diabetes (except gestational diabetes) or secondary diabetes;
    2. History of acute diabetic complications within 6 months prior to screening, such as diabetic ketoacidosis, hyperglycemic hyperosmolar state, or lactic acidosis;
    3. Having severe chronic complications of diabetes at screening, including but not limited to: proliferative diabetic retinopathy, severe diabetic macular edema, or severe non-proliferative diabetic retinopathy requiring treatment during the study period; intermittent claudication, diabetic foot ulcers; gastroparesis, painful neuropathy, a resting tachycardia, orthostatic hypotension;
    4. History of level 3 hypoglycemia within 6 months prior to screening (manifesting as central nervous system symptoms or abnormal changes in mental behavior);
    5. Has a personal history or first degree relative family history of multiple endocrine neoplasia syndrome type 2 (MEN2) or medullary thyroid carcinoma (MTC);
    6. Abnormal thyroid function that is not stably controlled with medication at screening (for at least 3 months);
    7. Having other serious endocrine system diseases that affect glucose metabolism, such as multiple endocrine neoplasia, Cushing's syndrome, etc.;
  • Any of the following medical history or evidence prior to screening:

    1. History of the following serious cardiovascular or cerebrovascular diseases within 6 months prior to screening: such as decompensated heart failure (New York Heart Association [NYHA] functional class III or IV), acute myocardial infarction, unstable angina attacks, or cardiac surgery such as coronary stent implantation or coronary artery bypass grafting (diagnostic angiography is permitted); new-onset stroke, transient ischemic attack, or recurrent syncope;
    2. Uncontrolled hypertension during screening: seated systolic blood pressure (SBP) ≥160 mmHg and/or seated diastolic blood pressure (DBP) ≥100 mmHg; or hypotension (SBP <90 mmHg);
    3. Have obvious hematologic diseases or any diseases that cause hemolysis or erythrocyte instability, including but not limited to: hemolytic anemia, aplastic anemia, myelodysplastic syndrome, thalassemia, etc.;
    4. Have a history of acute or chronic pancreatitis, symptomatic gallbladder or biliary tract disease (such as common bile duct stones, cholelithiasis with multiple stones, etc.; if the common bile duct stones have been cleared or the subject has previously undergone cholecystectomy, may be enrolled after assessment by the investigator), or a history of pancreatic injury and other high-risk factors that may lead to pancreatitis;
    5. Have a history of severe gastrointestinal diseases (such as active ulcer, inflammatory bowel disease) occurring within 6 months prior to screening, or have undergone gastrointestinal surgery (except appendectomy, polypectomy or other gastrointestinal endoscopic surgeries that are judged by the investigator to have no significant effect on gastrointestinal motility), or have clinically significant gastric emptying abnormalities(such as pyloric obstruction, intestinal obstruction, etc.), or have been taking drugs that directly affect gastrointestinal motility for a long time(such as domperidone, mosapride, cisapride, etc.);
    6. Severe trauma or acute infection within 4 weeks prior to screening that could potentially affect glycemic control;
    7. Any of the following clinically significant arrhythmias occurring at screening or randomization: second or third degree atrioventricular block, long QT syndrome, or other severe arrhythmias that the investigator deems unsuitable for inclusion in this study;
    8. History of malignant tumor within 5 years prior to screening (except clinically cured local skin basal cell carcinoma or carcinoma in situ); Comorbid psychiatric illness or language barriers, unwilling or unable to adequately understand and cooperate.
  • Use of any of the following medications or treatments prior to screening:

    1. Use of glucose-lowering medications other than metformin within 2 months prior to screening (except for cumulative duration ≤7 days);
    2. Use of GLP-1RA analogs or related compounds within 3 months prior to screening; known or suspected allergy to the investigational drug or related products; discontinued medication more than 3 months prior to screening due to intolerance or lack of efficacy must also be excluded;
    3. Use of weight-loss medications within 3 months prior to screening, or undergoing surgery that could lead to weight instability, or plan to undergo bariatric surgery or weight-loss procedures/surgical treatments during the trial; Currently receiving or having received chronic (>2 weeks) systemic glucocorticoid treatment within 3 months prior to screening (excluding topical, intraocular, intranasal, single intra-articular injection, or inhaled formulations), or having received such treatment within 4 weeks prior to screening.
  • Any of the following laboratory abnormalities at screening:

    1. Aspartate aminotransferase (AST) ≥3× upper limit of normal (ULN) and/or alanine aminotransferase (ALT) >3× ULN;
    2. Total bilirubin (TBIL) >1.5× ULN;
    3. Amylase and/or lipase ≥ 2×ULN;
    4. Estimated glomerular filtration rate (eGFR) < 45 mL/min/1.73 m² (estimated using the CKD-EPI formula) or urinary albumin to creatinine ratio(UACR) ≥ 300 mg/g;
    5. Triglycerides (TG) > 5.65 mmol/L;
    6. Calcitonin ≥ 50 ng/L;
    7. Thyroid-stimulating hormone (TSH) > 6.0 mIU/L or < 0.4 mIU/L; Positive result on hepatitis B surface antigen (HBsAg) and HBV-DNA quantitative test results above the upper limit of the local laboratory reference range, or positive hepatitis C virus antibody (HCV-Ab) and HCV-RNA test results above the upper limit of the local laboratory reference range, or positive human immunodeficiency virus(HIV) antibody, or positive treponema pallidum antibody.
  • History of substance abuse or alcohol abuse within 6 months prior to screening (consuming 14 units of alcohol per week: 1 unit = 285 mL of beer, 25 mL of spirits, or 100 mL of wine);

  • Participation in a clinical trial of another drug or medical device within 3 months prior to screening, and receipt of investigational medication or medical device intervention;

    • Undergoing major surgical treatment within 3 months prior to screening, or having elective surgery scheduled during the study period (excluding minor surgeries under local anesthesia);
  • Have donated blood or lost ≥400 mL of blood, received blood transfusion or used blood products within 3 months prior to screening; Pregnancy, lactation, or have tested positive for pregnancy; participants or their partners who are unwilling to use effective contraception from the time of signing the informed consent form until 3 months after the last dose.

  • Any other factor that, in the investigator's opinion, may affect the efficacy or safety assessment of this study or make the subject unsuitable for participation in this clinical trial (including, but not limited to, poor compliance as judged by the investigator, or living too far away to attend scheduled follow-up visits).

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Quadruplicar

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: SAL0150 group 1

SAL0150 tablets, use as specified in the protocol

SAL0150 tablets, use as specified in the protocol

Experimental: SAL0150 group 2

SAL0150 tablets, use as specified in the protocol

SAL0150 tablets,use as specified in the protocol

SAL0150 tablets, use as specified in the protocol

Experimental: SAL0150 group 3

SAL0150 tablets, use as specified in the protocol

SAL0150 tablets,use as specified in the protocol

SAL0150 tablets, use as specified in the protocol

Experimental: SAL0150 group 4

SAL0150 tablets, use as specified in the protocol

SAL0150 tablets, use as specified in the protocol

Experimental: SAL0150 group 5

SAL0150 tablets, use as specified in the protocol

SAL0150 tablets, use as specified in the protocol

Comparador de Placebo: Placebo Group

Placebo

Placebo

Comparador Ativo: Semaglutide inject Group

Semaglutide inject, 1.0 mg once weekly, 15 weeks

Semaglutide inject, 1.0 mg once weekly, 15 weeks

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
HbA1c
Prazo: Change From Baseline in HbA1c at Week 16(Baseline, Week 16)

HbA1c is measured to estimate average plasma glucose concentration

Change From Baseline in HbA1c at Week 16(Baseline, Week 16)

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
HbA1c
Prazo: Change from baseline in HbA1c (Baseline, Week 5, Week 9 and Week 13);

HbA1c is measured to estimate average plasma glucose concentration over the preceding 2-3 months

Change from baseline in HbA1c (Baseline, Week 5, Week 9 and Week 13);
Percentage of study participants achieving HbA1c < 7.0%, ≤ 6.5% or ≤ 5.7%
Prazo: Change from baseline to Week 16

Percentage of study participants achieving HbA1c < 7.0%, ≤ 6.5% or ≤ 5.7%(Week 16)

Change from baseline to Week 16

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

30 de outubro de 2026

Conclusão Primária (Estimado)

30 de novembro de 2027

Conclusão do estudo (Estimado)

30 de novembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

2 de novembro de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

2 de novembro de 2026

Primeira postagem (Real)

6 de novembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

2 de novembro de 2026

Última verificação

1 de novembro de 2026

Mais Informações

Termos relacionados a este estudo

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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