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A Randomized, Multi-center, Phase II Study of the Safety, Tolerability and Bioactivity of Repeated Intravitreal Injections of iCo-007 as Monotherapy or in Combination With Ranibizumab or Laser Photocoagulation in the Treatment of Diabetic Macular Edema (the iDEAL Study) (iDEAL)

28 de julho de 2017 atualizado por: Johns Hopkins University

A Randomized, Multi-center, Phase II Study of the Safety, Tolerability, and Bioactivity of Repeated Intravitreal Injections of iCo-007 as Monotherapy or in Combination With Ranibizumab or Laser Photocoagulation in the Treatment of Diabetic Macular Edema With Involvement of the FoveAL Center (the iDEAL Study)

  • To assess the safety of repeated iCo-007 intravitreal injections in treatment of subjects with diabetic macular edema as monotherapy and in combination with ranibizumab or laser photocoagulation
  • To assess the change in visual acuity and retinal thickness on optical coherence tomography (OCT) from baseline to month 8 and month 12

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Real)

185

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.

Locais de estudo

    • Nebraska
      • Omaha, Nebraska, Estados Unidos, 68198-5540
        • Stanley M Truhlsen Eye Institute

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:

  • Age ≥18 years
  • Have diabetes mellitus type I or II (insulin or non-insulin dependent) with HbA1c ≥5.5% and HbA1c ≤13%; have non-proliferative diabetic retinopathy, or inactive proliferative diabetic retinopathy, or proliferative diabetic retinopathy with a reasonable expectation that panretinal photocoagulation will not be required during the study follow-up period
  • Have diabetic macular edema with central subfield thickness of ≥250 microns (confirmed by Stratus Time-Domain(TD) OCT
  • Have best corrected visual acuity (ETDRS) that is Snellen equivalent of

    • 20/32 and ≥20/320, inclusive
  • Be willing and able to sign an approved written informed consent. If a patient has a central nervous system disorder (i.e. dementia) that will not allow him/her to understand the consent independently, the patient will not be allowed to join the study
  • Be able to attend all scheduled study visits
  • Women who are not lactating or pregnant and are willing to use adequate contraception during the study period, if appropriate

Exclusion Criteria:

  • Have macular or perimacular edema secondary to an etiology other than diabetes
  • Have concurrent retinal diseases other than diabetic retinopathy
  • Have additional ocular diseases compromising visual acuity and/or interfering with study assessments; patients who have glaucoma but deemed stable (intraocular pressure ≤ 25 mmHg at screening) on medications or status post surgery, may participate in the study
  • Participant has a history of prior pars plana vitrectomy
  • Subjects with significant cataract or or posterior capsular opacification that may need intervention within one year or vitreous opacity that hinder study assessment (i.e.fundus examination) which requires intervention within a year
  • Subjects who have DME with severe capillary non-perfusion (avascular zone diameter >1,000 microns)
  • Have an allergy to fluorescein dye
  • Have terminal renal disease (on active kidney dialysis), cerebral vascular accident(including TIA), myocardial infarction or congestive heart disease within 6 months of study enrollment, liver damage (2x upper limit of normal range for aspartate aminotransferase (AST), Alanine aminotransferase (ALT) or total bilirubin). Patients who may have received renal transplant in the past and now have stable renal function, may participate in the study
  • Subjects with systolic blood pressure higher than 180 mm Hg or diastolic above 100 mm Hg, with or without anti-hypertensive treatment
  • Have a history of panretinal photocoagulation (PRP) in the study eye within 3 months of study entry or are likely to have PRP in the study eye during study participation
  • Had macular photocoagulation or ocular surgery within 3 months of study entry in the study eye
  • Received intraocular or periocular injection of steroids in the study eye (e.g., triamcinolone) within 3 months of study entry or anti-angiogenic drugs (pegaptanib sodium, ranibizumab, bevacizumab, VEGF-TRAP, protein kinase C inhibitor, etc.) within 2 months of study entry; history of usage of topical or systemic steroids within 3 months of study entry is not an exclusion

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 fatorial
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Group 1

Drug: iCo-007 350 mcg

iCo-007 (350 μg) as an intravitreal injection at baseline followed by another iCo-007 dose (350 μg) at month 4

iCo-007 (350 μg) as an intravitreal injection at baseline followed by another iCo-007 dose (350 μg) at month 4
Outros nomes:
  • Grupo 1
Experimental: Group 2

Drug: iCo-007 700 mcg

iCo-007 (700 μg) as an intravitreal injection at baseline followed by another iCo-007 dose (700 μg) at month 4

iCo-007 (700 μg) as an intravitreal injection at baseline followed by another iCo-007 dose (700 μg) at month 4
Outros nomes:
  • Grupo 2
Experimental: Group 3

Drug: iCo-007 350 mcg and Laser

iCo-007 (350 μg) as an intravitreal injection at baseline followed 7 days later by laser photocoagulation. At M4, intravitreal injection of iCo-007 (350 μg) will be given as mandatory treatment. If the eye also meets retreatment criteria, it will also receive the second laser photocoagulation

iCo-007 (350 μg) as an intravitreal injection at baseline followed 7 days later by laser photocoagulation. At M4, intravitreal injection of iCo-007 (350 μg) will be given as mandatory treatment. If the eye also meets retreatment criteria, it will also receive the second laser photocoagulation
Outros nomes:
  • Grupo 3
Experimental: Group 4

Drug: Ranibizumab and iCo-007 350 mcg

Ranibizumab (0.5 mg) intravitreal injection at baseline followed by iCo-007 (350 μg) intravitreal injection 2 weeks later; re-treatment with ranibizumab (0.5 mg) mandatory at M4 followed by iCo-007 (350 μg) 2 weeks later

Ranibizumab (0.5 mg) intravitreal injection at baseline followed by iCo-007 (350 μg) intravitreal injection 2 weeks later; re-treatment with ranibizumab (0.5 mg) mandatory at M4 followed by iCo-007 (350 μg) 2 weeks later
Outros nomes:
  • Grupo 4

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in VA From Baseline to Month 8
Prazo: Baseline to month 8
The primary efficacy variable is the change in visual acuity (mean change in number of letters) from baseline to month 8
Baseline to month 8

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Number of Participants in a Given Study Arm Experiencing the Same Drug-related Serious Adverse Event as a Measure of Safety and Tolerability
Prazo: Baseline to month 8
Safety of repeated iCo-007 intravitreal injections in treatment of subjects with Diabetic Macular Edema (DME) as monotherapy and in combination with ranibizumab or laser photocoagulation. Serious consideration will be given if 2 or more patients in a particular treatment arm experience the same drug-related serious adverse event;
Baseline to month 8
Change in VA From Baseline to Month 12
Prazo: Baseline to month 12
The primary efficacy variable is the change in visual acuity (mean change in number of letters) from baseline to month 12
Baseline to month 12
Change in Retinal Thickness Measured by OCT From Baseline to Month 8
Prazo: Baseline to month 8
Group 1
Baseline to month 8
Change in Retinal Thickness Measured
Prazo: Baseline to month 12
measured by OCT
Baseline to month 12
Duration of iCo-007 Treatment Effect
Prazo: Baseline to month 12
treatment effect as measured by VA and OCY thickness
Baseline to month 12
Peak Plasma Concentration (Cmax)of iCo-007 After Multiple Injections
Prazo: Baseline to month 12
cmax
Baseline to month 12

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Diana V. Do, MD, Stanley M Truhlsen Eye Institute, University of Nebraska Medical Center
  • Investigador principal: Robert Wong, MD, Austin Retina Associates
  • Investigador principal: Michael J. Tolentino, MD, Center for Retina Macula Disease
  • Investigador principal: Prema Abraham, MD, Black Hills Regional Eye Institute
  • Investigador principal: Eugene Lit, MD, East Bay Retina Institute
  • Investigador principal: Michael J. Elman, MD, Elman Retina Group
  • Investigador principal: Thomas A. Barnard, MD, Florida Retina Institute
  • Investigador principal: Thomas A. Ciulla, MD, Midwest Eye Institute
  • Investigador principal: Richard B. Rosen, MD, New York Eye and Ear Infirmary
  • Investigador principal: Henry L. Hudson, MD, Retina Centers, P.C.
  • Investigador principal: Pravin Dugel, MD, Retina Consultants of Arizona
  • Investigador principal: Gregg T. Kokame, MD, Retina Consultants of Hawaii, Pali Momi Medical Center
  • Investigador principal: David M. Brown, MD, Retina Consultants Houston
  • Investigador principal: Larry S. Halperin, MD, Retina Group of Florida
  • Investigador principal: Goergios Papastergio, MD, Retina Institute of Hawaii
  • Investigador principal: Ron P. Gallemore, MD. PhD, Retina Macula Institute
  • Investigador principal: Brian B. Berger, MD, Retina Research Center
  • Investigador principal: Homayoun Tabandeh, MD, Retina Vitreous Associates
  • Investigador principal: Dennis M. Marcus, MD, Southeast Retina
  • Investigador principal: Robert S. Wirthlin, MD, Spokane Eye Clinic
  • Investigador principal: David Callanan, MD, Texas Retina Associates in Arlington
  • Investigador principal: Karl G. Csaky, MD, PhD, Texas Retina Associates in Dallas
  • Investigador principal: Surendar Purohit, MD, TLC Eye Care & Laser Center
  • Investigador principal: Victor H. Gonzalez, MD, Valley Retina Institute
  • Investigador principal: Louis Glazer, MD, Vitreo-Retinal Associates
  • Investigador principal: Dean Eliott, MD, Massachusetts Eye and Ear Infirmary, Harvard Medical School

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)

1 de fevereiro de 2012

Conclusão Primária (Real)

1 de fevereiro de 2014

Conclusão do estudo (Real)

1 de outubro de 2014

Datas de inscrição no estudo

Enviado pela primeira vez

15 de março de 2012

Enviado pela primeira vez que atendeu aos critérios de CQ

26 de março de 2012

Primeira postagem (Estimativa)

28 de março de 2012

Atualizações de registro de estudo

Última Atualização Postada (Real)

30 de agosto de 2017

Última atualização enviada que atendeu aos critérios de controle de qualidade

28 de julho de 2017

Última verificação

1 de julho de 2017

Mais Informações

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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