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A Phase 3, Randomized, Double-masked, Parallel-assignment Study of Intravitreal Bevasiranib Sodium, Administered Every 8 or 12 Weeks as Maintenance Therapy Following Three Injections of Lucentis® Compared With Lucentis® Monotherapy Every 4 Weeks in Patients With Exudative Age-Related Macular Degeneration (AMD).

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Trial Profile

A Phase 3, Randomized, Double-masked, Parallel-assignment Study of Intravitreal Bevasiranib Sodium, Administered Every 8 or 12 Weeks as Maintenance Therapy Following Three Injections of Lucentis® Compared With Lucentis® Monotherapy Every 4 Weeks in Patients With Exudative Age-Related Macular Degeneration (AMD).

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 12 Nov 2014

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At a glance

  • Drugs Bevasiranib (Primary) ; Ranibizumab
  • Indications Age-related macular degeneration
  • Focus Registrational; Therapeutic Use
  • Acronyms COBALT
  • Sponsors OPKO Health

    • Most Recent Events

    • 26 May 2014 New trial record

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