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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 juli 2017 bijgewerkt door: 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

Studie Overzicht

Studietype

Ingrijpend

Inschrijving (Werkelijk)

185

Fase

  • Fase 2

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Nebraska
      • Omaha, Nebraska, Verenigde Staten, 68198-5540
        • Stanley M Truhlsen Eye Institute

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Faculteitstoewijzing
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: 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
Andere namen:
  • Groep 1
Experimenteel: 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
Andere namen:
  • Groep 2
Experimenteel: 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
Andere namen:
  • Groep 3
Experimenteel: 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
Andere namen:
  • Groep 4

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Change in VA From Baseline to Month 8
Tijdsspanne: 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

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Number of Participants in a Given Study Arm Experiencing the Same Drug-related Serious Adverse Event as a Measure of Safety and Tolerability
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: Baseline to month 8
Group 1
Baseline to month 8
Change in Retinal Thickness Measured
Tijdsspanne: Baseline to month 12
measured by OCT
Baseline to month 12
Duration of iCo-007 Treatment Effect
Tijdsspanne: 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
Tijdsspanne: Baseline to month 12
cmax
Baseline to month 12

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

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

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

1 februari 2012

Primaire voltooiing (Werkelijk)

1 februari 2014

Studie voltooiing (Werkelijk)

1 oktober 2014

Studieregistratiedata

Eerst ingediend

15 maart 2012

Eerst ingediend dat voldeed aan de QC-criteria

26 maart 2012

Eerst geplaatst (Schatting)

28 maart 2012

Updates van studierecords

Laatste update geplaatst (Werkelijk)

30 augustus 2017

Laatste update ingediend die voldeed aan QC-criteria

28 juli 2017

Laatst geverifieerd

1 juli 2017

Meer informatie

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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