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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 luglio 2017 aggiornato da: 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

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Effettivo)

185

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Nebraska
      • Omaha, Nebraska, Stati Uniti, 68198-5540
        • Stanley M Truhlsen Eye Institute

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione fattoriale
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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
Altri nomi:
  • Gruppo 1
Sperimentale: 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
Altri nomi:
  • Gruppo 2
Sperimentale: 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
Altri nomi:
  • Gruppo 3
Sperimentale: 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
Altri nomi:
  • Gruppo 4

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Change in VA From Baseline to Month 8
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of Participants in a Given Study Arm Experiencing the Same Drug-related Serious Adverse Event as a Measure of Safety and Tolerability
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: Baseline to month 8
Group 1
Baseline to month 8
Change in Retinal Thickness Measured
Lasso di tempo: Baseline to month 12
measured by OCT
Baseline to month 12
Duration of iCo-007 Treatment Effect
Lasso di tempo: 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
Lasso di tempo: Baseline to month 12
cmax
Baseline to month 12

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

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

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

1 febbraio 2012

Completamento primario (Effettivo)

1 febbraio 2014

Completamento dello studio (Effettivo)

1 ottobre 2014

Date di iscrizione allo studio

Primo inviato

15 marzo 2012

Primo inviato che soddisfa i criteri di controllo qualità

26 marzo 2012

Primo Inserito (Stima)

28 marzo 2012

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

30 agosto 2017

Ultimo aggiornamento inviato che soddisfa i criteri QC

28 luglio 2017

Ultimo verificato

1 luglio 2017

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Edema maculare diabetico

Prove cliniche su iCo-007 350 mcg

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