A 24 Month Phase 2a Open Label, Randomized Study of Avastin®, Lucentis®, or Eylea® (Anti-VEGF Therapy) Administered in Combination With Fovista® (Anti-PDGF BB Pegylated Aptamer)

Part of paid clinical trials in Phoenix, Arizona.

Sponsor
Ophthotech Corporation
Study ID
NCT02387957
Phase
PHASE2
Status
Terminated

Conditions

Eligibility Criteria

Sex
ALL
Age
50 Years - N/A
Healthy Volunteers
Not accepted

Interventions

Study Details

To evaluate the safety of intravitreal (IVT) Fovista® administered in combination with anti-VEGF therapy.

Key Dates

Start date
Apr 26, 2016
Status verified
Feb 2019
Primary completion
Jan 31, 2017
Completion
Jan 31, 2017

Study Design

Enrollment
63 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Fovista® plus bevacizumab
    Fovista® 1.5 mg intravitreal injection + bevacizumab 1.25 mg intravitreal injection
  • Experimental: Fovista® plus ranibizumab
    Fovista® 1.5 mg intravitreal injection + 0.5 mg ranibizumab intravitreal injection
  • Experimental: Fovista® plus aflibercept
    Fovista® 1.5 mg intravitreal injection + 2.0 mg aflibercept intravitreal injection

Primary Outcome Measure

Total Numer of Systemic Adverse Events [ Time Frame: 2 years ]

Locations (24)

FacilityCityStateZIPSite coordinators
-PhoenixArizona85014-
-Beverly HillsCalifornia90211-
-SacramentoCalifornia95819-
-Santa AnaCalifornia92705-
-New LondonConnecticut06320-
-Fort LauderdaleFlorida33308-
-Fort MyersFlorida33912-
-AugustaGeorgia30909-
-Oak ForestIllinois60452-
-BostonMassachusetts02114-
-WorcesterMassachusetts01605-
-SouthfieldMichigan48034-
-MinneapolisMinnesota55435-
-RenoNevada89502-
-RochesterNew York14620-
-ClevelandOhio44130-
-Huntingdon ValleyPennsylvania19006-
-LadsonSouth Carolina29456-
-AbileneTexas85014-
-AmarilloTexas79106-
-San AntonioTexas78240-
-The WoodlandsTexas77384-
-SilverdaleWashington98383-
-MorgantownWest Virginia26506-

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