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A Phase 1b Study to Assess the Safety and Anti-inflammatory Effects of Two Different Doses of SRT2104 in Patients With Ulcerative Colitis

31 de maio de 2017 atualizado por: Sirtris, a GSK Company

A Phase 1b, Exploratory Study to Assess the Safety, Tolerability, Colonic Tissue Exposure, and Anti-Inflammatory Effects of Two Different Doses of SRT2104 in Subjects With Mild to Moderate Ulcerative Colitis

The purpose of this research study is to:

  • 1) Test the safety and tolerability of 2 different oral doses of SRT2104 in subjects with ulcerative colitis
  • 2) Determine the amount of SRT2104 measured from a single blood sample in addition to colon and/or rectal tissue samples (biopsies)
  • 3) Determine whether SRT2104 has any anti-inflammatory effect on the colon and/or rectum when taken orally for 8 weeks
  • 4) Determine whether SRT2104 causes any detectable changes to specific biomarkers. A biomarker is a biological marker (or substance such as a protein) that is used as an indicator of changes in a biological state that corresponds to the risk or progression of a disease.

Visão geral do estudo

Status

Concluído

Condições

Intervenção / Tratamento

Tipo de estudo

Intervencional

Inscrição (Real)

17

Estágio

  • Fase 1

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.

Locais de estudo

  • Estados Unidos
    • California
      • Anaheim, California, Estados Unidos, 92801
        • GSK Investigational Site
    • Connecticut
      • Bristol, Connecticut, Estados Unidos, 06010
        • GSK Investigational Site
    • Kentucky
      • Owensboro, Kentucky, Estados Unidos, 42303
        • GSK Investigational Site
    • Maryland
      • Chevy Chase, Maryland, Estados Unidos, 20815
        • GSK Investigational Site
      • Towson, Maryland, Estados Unidos, 21204
        • GSK Investigational Site
    • Michigan
      • Chesterfield, Michigan, Estados Unidos, 48047
        • GSK Investigational Site
    • New York
      • Great Neck, New York, Estados Unidos, 11021
        • GSK Investigational Site
      • New York, New York, Estados Unidos, 10029
        • GSK Investigational Site
    • North Carolina
      • Raleigh, North Carolina, Estados Unidos, 27612
        • GSK Investigational Site
    • Ohio
      • Beavercreek, Ohio, Estados Unidos, 45432
        • GSK Investigational Site
      • Columbus, Ohio, Estados Unidos, 43215
        • GSK Investigational Site
    • Oklahoma
      • Oklahoma City, Oklahoma, Estados Unidos, 73104
        • GSK Investigational Site
    • Tennessee
      • Jackson, Tennessee, Estados Unidos, 38305
        • GSK Investigational Site

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 a 75 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Mild to moderately active ulcerative colitis as evidenced by Mayo score 6-10 (inclusive) with rectal bleeding score ≥1, endoscopy score between 2-3 (inclusive), and physician's rating of disease activity <3 at Day -5
  • Colonic inflammation extending proximal to the rectum (i.e., greater than 15 cm in extent) on baseline sigmoidoscopy at Day -5
  • Confirmed diagnosis of ulcerative colitis for at least 3 months prior to the Screening Visit (Visit 1)
  • Male or female between 18 and 75 years, inclusive
  • Body weight >50 kg and BMI ≥18 kg/m^2 at Screening (Visit 1)
  • Capable of giving written informed consent, and willing and able to comply with the requirements of the protocol
  • Female subjects of child-bearing potential must be willing to use reliable contraception from Visit 1 through the follow-up visit (Day 70)

Exclusion Criteria:

  • Suspicion of Crohn's disease, indeterminate colitis, microscopic colitis, segmental colitis associated with diverticulosis, ischemic colitis, or radiation-induced colitis based on medical history, endoscopy, and/or histological findings
  • Presence of infectious colitis as evidenced by positive stool culture for enteric pathogens or positive stool Clostridium difficile cytotoxin assay at Visit 1
  • Presence of chronic liver disease, with the exception of known Gilbert's syndrome
  • A positive pre-study Hepatitis B surface antigen, Hepatitis C antibody or HIV at Visit 1
  • Past or present disease that is judged by the investigator to have the potential to interfere with the study procedures or compromise the subject's safety
  • History of malignant neoplasm within the past 5 years, other than localized basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ that has been resected or definitively treated with standard approaches
  • Prior diagnosis of flat colonic dysplasia or unresected raised colonic dysplasia (adenoma-like lesion or mass)
  • History of regular alcohol consumption within 6 months of the Screening (Visit 1) defined as an average weekly intake of >14 drinks (one drink is defined as 12 ounces of beer, 5 ounces of wine, or 1.5 ounces of 80 proof distilled spirits) or presence of recreational drug abuse or dependence
  • Known bleeding disorders
  • Bowel surgery within 12 months prior to Visit 1
  • History of colectomy or partial colectomy
  • Treatment with oral aminosalicylates at doses >4.8 g per day or aminosalicylate dose modification (except transient shift lasting up to 3 days) within 4 weeks prior to study Day -5 (Note: if on this type of treatment, the dose must remain constant throughout the study treatment period)
  • Treatment with rectal aminosalicylates at any dose within 2 weeks of study Day -5
  • Treatment with systemic or rectal corticosteroids within 4 weeks of study Day -5
  • Treatment with TNFα inhibitors or other biologics within 2 months prior to study Day -5
  • Treatment with other immunosuppressants (azathioprine or 6-mercaptopurine), if initiated within 3 months prior to study Day -5, or if changed in terms of dose within 3 months prior to study Day -5 (Note: if on this type of treatment, the dose must remain constant throughout the study treatment period)
  • Regular use of pro-biotic or prebiotic preparations within 4 weeks of study Day -5 visit
  • Regular use of non-steroidal anti-inflammatories (NSAIDS) or aspirin, except low dose (cardioprotective ≤325 mg/day) aspirin, within 7 days prior to study Day -5
  • Participation in a clinical trial and treatment with an study drug within 3 months prior to Visit 1
  • Have a clinically significant finding on a chest X-ray performed at Visit 1 or within 3 months of Visit 1
  • Have an abnormal 12-lead electrocardiogram (ECG) with one or more changes considered to be clinically significant on medical review

  • Renal or liver impairment based on laboratory values obtained at Visit 1 and defined as:

    • serum creatinine level of ≥1.4 mg/dL for females and ≥1.5 mg/dL for males, or
    • AST and/or ALT ≥2x upper limit of normal (ULN), or
    • bilirubin > 1.5xULN (an isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin is <35%)
    • Hemoglobin less than 8.5 g/dL at Visit 1
    • Have any other reason which, in the opinion of the investigator, would confound the conduct or interpretation of the study

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: 50mg SRT2104
Single oral administration of 50mg SRT2104 study drug will be supplied as 25 mg and 250 mg capsules and will be taken orally once daily for 56 days. SRT2104 is to be taken at approximately the same time every morning, in the fasted state. Water is permitted ad libitum. Subjects are allowed to consume liquids but should refrain from eating solid food for approximately 1 hour after dosing.
Medicamento: SRT2104
SRT2104 drug substance is a new chemical entity which is supplied as a fine, yellowish/amber powder. The SRT2104 investigational product is prepared by packing 25mg or 250 mg of micronized SRT2104 powder with no additional additives into a size 00 opaque, hard gelatin capsule. All subjects will be provided with one dosing bottle per day that contains two 25 mg or 250 mg SRT2104 capsules for oral ingestion.
Experimental: 500mg SRT2104
Single oral administration of 500mg SRT2104 will be taken orally once daily for 56 days. SRT2104 is to be taken at approximately the same time every morning, in the fasted state. Water is permitted ad libitum. Subjects are allowed to consume liquids but should refrain from eating solid food for approximately 1 hour after dosing.
Medicamento: SRT2104
SRT2104 drug substance is a new chemical entity which is supplied as a fine, yellowish/amber powder. The SRT2104 investigational product is prepared by packing 25mg or 250 mg of micronized SRT2104 powder with no additional additives into a size 00 opaque, hard gelatin capsule. All subjects will be provided with one dosing bottle per day that contains two 25 mg or 250 mg SRT2104 capsules for oral ingestion.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Prazo
Number of participants with adverse events and incidence of adverse events will be used as a measure of safety and tolerability of 50 mg and 500 mg of SRT2104 after repeat dosing for up to eight weeks in subjects with mild to moderate ulcerative colitis
Prazo: 75 days
75 days
SRT2104 concentration in colonic tissue will be measured via endoscopic biopsy after repeat dosing for up to 8 weeks in subjects with mild to moderate ulcerative colitis
Prazo: 56 days
56 days

Medidas de resultados secundários

Medida de resultado
Prazo
Endoscopic scoring of colonic lesions assessed during flexible sigmoidoscopy will be used as a measure of the anti-inflammatory effect of SRT2104 after 8 weeks of treatment in subjects with mild to moderate ulcerative colitis
Prazo: 75 days
75 days
Mayo score and Partial Mayo score will be used as a measure of the anti-inflammatory effect of SRT2104 after 8 weeks of treatment in subjects with mild to moderate ulcerative colitis
Prazo: 75 days
75 days
Simple Clinical Colitis Activity Index (SCCAI) will be used as a measure of the anti-inflammatory effect of SRT2104 after 8 weeks of treatment in subjects with mild to moderate ulcerative colitis
Prazo: 75 days
75 days
Fecal calprotectin will be used as a measure of the anti-inflammatory effect of SRT2104 after 8 weeks of treatment in subjects with mild to moderate ulcerative colitis
Prazo: 75 days
75 days
Histopathologic scoring of colonic tissue biopsies obtained via flexible sigmoidoscopy will be used as a measure of the anti-inflammatory effect of SRT2104 after 8 weeks of treatment in subjects with mild to moderate ulcerative colitis
Prazo: 75 days
75 days
SRT2104 concentration in plasma will be measured after repeat dosing for up to 8 weeks in subjects with mild to moderate ulcerative colitis
Prazo: 56 days
56 days

Colaboradores e Investigadores

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

Patrocinador

Sirtris, a GSK Company

Colaboradores

GlaxoSmithKline

Publicações e links úteis

A pessoa responsável por inserir informações sobre o estudo fornece voluntariamente essas publicações. Estes podem ser sobre qualquer coisa relacionada ao estudo.

Publicações Gerais

Links úteis

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 (Real)

13 de fevereiro de 2012

Conclusão Primária (Real)

18 de março de 2013

Conclusão do estudo (Real)

18 de março de 2013

Datas de inscrição no estudo

Enviado pela primeira vez

13 de outubro de 2011

Enviado pela primeira vez que atendeu aos critérios de CQ

13 de outubro de 2011

Primeira postagem (Estimativa)

18 de outubro de 2011

Atualizações de registro de estudo

Última Atualização Postada (Real)

1 de junho de 2017

Última atualização enviada que atendeu aos critérios de controle de qualidade

31 de maio de 2017

Última verificação

1 de maio de 2017

Mais Informações

Termos relacionados a este estudo

Termos MeSH relevantes adicionais

Outros números de identificação do estudo

  • 115951

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

Sim

Descrição do plano IPD

Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.

Dados/documentos do estudo

  1. Protocolo de estudo
    Identificador de informação: 115951
    Comentários informativos: For additional information about this study please refer to the GSK Clinical Study Register
  2. Relatório de Estudo Clínico
    Identificador de informação: 115951
    Comentários informativos: For additional information about this study please refer to the GSK Clinical Study Register
  3. Conjunto de dados de participantes individuais
    Identificador de informação: 115951
    Comentários informativos: For additional information about this study please refer to the GSK Clinical Study Register
  4. Plano de Análise Estatística
    Identificador de informação: 115951
    Comentários informativos: For additional information about this study please refer to the GSK Clinical Study Register
  5. Especificação do conjunto de dados
    Identificador de informação: 115951
    Comentários informativos: For additional information about this study please refer to the GSK Clinical Study Register
  6. Formulário de Consentimento Informado
    Identificador de informação: 115951
    Comentários informativos: For additional information about this study please refer to the GSK Clinical Study Register
  7. Formulário de Relato de Caso Anotado
    Identificador de informação: 115951
    Comentários informativos: For additional information about this study please refer to the GSK Clinical Study Register

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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