A PARALLEL-GROUP PHASE 4, OPEN-LABEL, TWO-ARM STUDY TO ASSESS THE SAFETY ANDEFFICACY OF INTRAVITREAL (IVT) AFLIBERCEPT WITH PROACTIVE CUSTOMIZED TREATMENT INTERVALS IN PATIENTS ¿50 YEARS OF AGE WITH NO FLUID DUE TO CHOROIDAL NEOVASCULARIZATION (CNV) LESIONS SECONDARY TO NEOVASULAR (WET) AGE-RELATED MACULAR DEGENERATION (NAMD) FOLLOWING TREATMENT INITIATION WITH AFLIBERCEPT

Registry ID
21912
Source registry
HEALTH_CANADA
Status
Closed
Phase
PHASE4
Study type
INTERVENTIONAL
Sponsor
BAYER INC
Start date
2023-03-07
Completion date
2023-07-16
Last update
2022-09-07

Conditions

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