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- Ensaio Clínico NCT00762684
Efficacy and Safety Study of TAK-559 in Treating Subjects With Type 2 Diabetes Mellitus
A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel Study of the Safety and Efficacy of TAK-559 Compared to Placebo in the Treatment of Patients With Type 2 Diabetes Mellitus
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Insulin is a primary regulator of blood glucose concentrations. A subnormal response to circulating insulin levels at target tissues leads to a decrease in insulin-mediated glucose uptake. Insulin resistance is associated with normal to high insulin levels and is often accompanied by dyslipidemia, a disruption in lipid metabolism resulting in increased triglycerides and low-density lipoprotein levels as well as decreased high-density lipoprotein levels in patients with type 2 diabetes mellitus. In the early stages of insulin resistance, a compensatory mechanism of increased insulin secretion by the pancreas maintains normal to near-normal glucose levels. Once the pancreas fails to maintain the increased insulin output, overt type 2 diabetes mellitus occurs.
TAK-559 is a novel oxyiminoalkanoic acid under investigation for use as an oral agent in the treatment of patients with type 2 diabetes mellitus. TAK-559 has partial peroxisome proliferator-activated receptor-alpha agonist activity, potent peroxisome proliferator-activated receptor-alpha activity, and modest peroxisome proliferator-activated receptor-gamma activity at high concentrations in nonclinical models.
This study was designed to evaluate the safety and glycemic control of TAK-559 in patients with type 2 diabetes mellitus whose symptoms were managed by diet and exercise.
Tipo de estudo
Inscrição (Real)
Estágio
- Fase 3
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
Aceita Voluntários Saudáveis
Gêneros Elegíveis para o Estudo
Descrição
Inclusion Criteria:
- Was diagnosed with type 2 diabetes mellitus using American Diabetes Association diagnostic criteria, and on a stable dose of an oral anti-diabetic monotherapy prior to Screening A.
- Had a glycosylated hemoglobin level greater than or equal to 8.0% and less than or equal to 10.0% at Screening B.
- Had a fasting plasma glucose greater than or equal to 126 mg/dL (7.0 mmol/L) at Screening B.
- Was taking a stable dose of at least 10 mg of glyburide for at least 10 days prior to Screening B.
- Had a stable or worsening self-monitoring blood glucose level while taking glyburide.
- Had a low-density lipoprotein less than 160 mg/dL (4.1 mmol/L) at Screening A.
- Had a body mass index less than or equal to 45 kg/m2 at Screening A.
- Was willing to be counseled by the investigator or designee to follow an individualized, weight-maintaining diet during the study period.
- Had evidence of insulin secretory capacity as demonstrated by a C-peptide concentration of greater than or equal to 1.5 ng/mL (0.50 nmol/L) at Screening A, and if necessary, after a repeat at Screening B.
- Was able to perform daily self-monitoring blood glucose tests throughout the study.
- Had a normal thyroid-stimulating hormone level of less than 5.5 uIU/mL (5.5 mIU/L) and greater than or equal to 0.35 uIU/mL (0.35 mIU/L) at Screening A.
- Was in good health as determined by a physician (ie, via medical history and physical examination), other than a diagnosis of type 2 diabetes mellitus.
- Had fasting clinical laboratory evaluations within the normal reference range for the testing laboratory, or if not, the results must be deemed not clinically significant by the investigator prior to Randomization.
- Females were post menopausal, surgically sterile, or using adequate contraception.
Exclusion Criteria:
- Had been diagnosed with type 1 diabetes mellitus, hemochromatosis, or has a history of ketoacidosis.
- Had any condition known to invalidate glycosylated hemoglobin results (eg, hemolytic states, hemoglobinopathies).
Was required to take or intends to continue taking any disallowed medication, any prescription medication, herbal treatment or over-the counter medication that may interfere with evaluation of the study medication, including:
- Insulin
- Oral anti-diabetics other than TAK-559 (including sulfonylureas other than glyburide, alpha-glucosidase inhibitors, metformin)
- Systemic corticosteroids
- Warfarin
- Rifampin
- St. John's Wort.
- Thiazolidinediones
- Peroxisome proliferator-activated receptor agonists
- Nicotinic Acid
- Fibrates
- Had a history of myocardial infarction, coronary angioplasty or bypass graft, unstable angina pectoris, transient ischemic attacks, clinically significant abnormal electrocardiogram, or documented cerebrovascular accident within 6 months prior to Screening A.
- Had abdominal, thoracic, or vascular surgery within 6 months prior to Screening A that in the investigator's opinion would warrant exclusion from the study.
- Had a creatine phosphokinase value greater than 3 times the upper limit of normal at Screening A. The creatine phosphokinase value can be retested prior to Randomization if elevated.
- Had persistent unexplained microscopic or macroscopic hematuria or a history of bladder cancer.
- Had a triglyceride level greater than 500 mg/dL (5.6 mmol/L) at Screening A.
- Had any alteration in allowed lipid lowering medication (dose or drug) within 2 months of Randomization, if applicable.
- Had donated and/or received any blood or blood products within 3 months prior to Randomization.
- Had a history of drug abuse (defined as illicit drug use) or a history of alcohol abuse (defined as regular or daily consumption of more than 4 alcoholic drinks per day) within 2 years prior to Randomization.
- Had a systolic BP greater than 140 mm Hg or a diastolic blood pressure of greater than 95 mm Hg at Screening B.
- Had significant cardiovascular disease including but not limited to, New York Heart Association Functional (Cardiac) Classification III or IV.
- Had a previous history of cancer, other than basal cell or stage 1 squamous cell carcinoma of the skin, that has not been in remission within 5 years prior to Randomization.
- Had an alanine transaminase or aspartate transaminase level greater than 3 times the upper limit of normal, active liver disease, or jaundice at Screening A.
- Had a positive human immunodeficiency virus, hepatitis B surface antigen, or hepatitis B e antigen test at Screening A.
- Had any other serious disease or condition at Screening A or at Randomization that might affect life expectancy or make it difficult to successfully manage and follow the patient according to the protocol.
Plano de estudo
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 |
|---|---|
|
Comparador de Placebo: Placebo QD
|
TAK-559 comprimidos correspondentes ao placebo, por via oral, uma vez ao dia por até 26 semanas.
|
|
Experimental: TAK-559 32 mg QD
|
TAK-559 32 mg, comprimidos, via oral, uma vez ao dia por até 26 semanas.
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Prazo |
|---|---|
|
Mudança da linha de base na hemoglobina glicosilada.
Prazo: Última Visita.
|
Última Visita.
|
Medidas de resultados secundários
Medida de resultado |
Prazo |
|---|---|
|
Mudança da linha de base na glicose plasmática em jejum.
Prazo: Semanas 2, 4, 8, 12, 16, 20 e visita final
|
Semanas 2, 4, 8, 12, 16, 20 e visita final
|
|
Mudança da linha de base na insulina sérica.
Prazo: Semanas 4, 12, 16, 20 e Visita Final.
|
Semanas 4, 12, 16, 20 e Visita Final.
|
|
Mudança da linha de base no peptídeo C.
Prazo: Semanas 4, 12, 16, 20 e Visita Final.
|
Semanas 4, 12, 16, 20 e Visita Final.
|
|
Mudança da linha de base em triglicerídeos.
Prazo: Semanas 12, 16, 20 e Visita Final.
|
Semanas 12, 16, 20 e Visita Final.
|
|
Mudança da linha de base no colesterol total.
Prazo: Semanas 12, 16, 20 e Visita Final.
|
Semanas 12, 16, 20 e Visita Final.
|
|
Mudança da linha de base na lipoproteína de alta densidade.
Prazo: Semanas 12, 16, 20 e Visita Final.
|
Semanas 12, 16, 20 e Visita Final.
|
|
Mudança da linha de base na lipoproteína de baixa densidade.
Prazo: Semanas 12, 16, 20 e Visita Final.
|
Semanas 12, 16, 20 e Visita Final.
|
|
Mudança da linha de base na lipoproteína de densidade muito baixa.
Prazo: Semanas 12, 16, 20 e Visita Final.
|
Semanas 12, 16, 20 e Visita Final.
|
|
Mudança da linha de base em ácidos graxos livres.
Prazo: Semanas 12, 16, 20 e Visita Final.
|
Semanas 12, 16, 20 e Visita Final.
|
|
Mudança da linha de base na proporção de albumina urinária para creatinina.
Prazo: Semanas 12, 16, 20 e visita final
|
Semanas 12, 16, 20 e visita final
|
|
Change from baseline in glycosylated hemoglobin.
Prazo: Weeks 4, 8, 12, 16 and 20
|
Weeks 4, 8, 12, 16 and 20
|
|
Change from base line in apolipoproteins A1 and B 100.
Prazo: Final Visit
|
Final Visit
|
|
Change from baseline in thrombosis marker (plasminogen activator inhibitor-1)
Prazo: Weeks 4, 12, 16, 20 and Final Visit
|
Weeks 4, 12, 16, 20 and Final Visit
|
|
Change from baseline in thrombosis marker (fibrinogen)
Prazo: Weeks 4, 12, 16, 20 and Final Visit
|
Weeks 4, 12, 16, 20 and Final Visit
|
|
Change from baseline in inflammation marker (Interleukin-6).
Prazo: Weeks 4, 12, 16, 20 and Final Visit
|
Weeks 4, 12, 16, 20 and Final Visit
|
|
Change from baseline in inflammation marker (C-reactive protein).
Prazo: Weeks 4, 12, 16, 20, and Final Visit
|
Weeks 4, 12, 16, 20, and Final Visit
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo
Conclusão Primária (Real)
Conclusão do estudo (Real)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Estimativa)
Atualizações de registro de estudo
Última Atualização Postada (Estimativa)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 01-04-TL-559-028
- U1111-1127-7965 (Identificador de registro: WHO)
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