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Clinical Trial Summary

LT1009-Oph-002 is a Phase 1b study designed to evaluate the safety and potential efficacy of iSONEP following one, two or three injections of iSONEP, as needed, for the treatment of Pigment Epithelial Detachment (PED) secondary to PED Secondary to Exudative Age-Related Macular Degeneration (AMD) or Polypoidal Choroidal Vasculopathy (PCV).


Clinical Trial Description

Sixteen (16) subjects per dose group who have received a minimum of 3 and no more than 7 doses of an anti-VEGF agent (i.e., Lucentis or Avastin), and whose PED has not decreased by greater than 25% in height despite therapy, will be enrolled for a total of 32 subjects. The presence of PED diagnosed by the Investigator will be confirmed by SDOCT, ICG and FA by a digital imaging reading center prior to subject enrollment. The ability of iSONEP to induce regression of persistent PED in subjects with exudative AMD or PCV despite previous treatment with an anti-VEGF agent will be evaluated. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01334255
Study type Interventional
Source Lpath, Inc.
Contact
Status Terminated
Phase Phase 1
Start date March 2011
Completion date July 2012

See also
  Status Clinical Trial Phase
Completed NCT00590694 - Lucentis for Age-related Macular Degeneration Pigment Epithelial Detachments Phase 2/Phase 3
Completed NCT00976222 - Intravitreal Ranibizumab in Retinal Pigment Epithelial Detachments Phase 4
Completed NCT00841581 - Lucentis to Treat Pigment Epithelial Detachment Phase 2
Active, not recruiting NCT01670162 - On-label tReatment With Intravitreal Aflibercept injectiOn for Patients With Persistent Pigment epitheliaL Detachments in Neovascular Age Related Macular Degeneration (AMD) Phase 4
Completed NCT03370380 - Aflibercept in Patients With Pigment Epithelial Detachments (PED)