Viewing Study NCT00857259


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Study NCT ID: NCT00857259
Status: TERMINATED
Last Update Posted: 2011-08-19
First Post: 2009-03-04
Is Gene Therapy: True
Has Adverse Events: True

Brief Title: The Efficacy of Oral Everolimus in Patients With Neovascular Age-related Macular Degeneration
Sponsor: Novartis Pharmaceuticals
Organization:

Study Overview

Official Title: A Randomized, Double-masked, Parallel Group Study to Assess the Efficacy of Oral Everolimus, Either Alone or Added to Lucentis, in Patients With Neovascular Age-related Macular Degeneration
Status: TERMINATED
Status Verified Date: 2011-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The study will assess the safety and efficacy of Everolimus (RAD001) alone or in combination with Lucentis in patients with neo-vascular age related macular degeneration (AMD)
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
EudraCT number: 2008-003550-15 None None View