Study to Assess the Efficacy and Safety of Brolucizumab 6mg Compared to Aflibercept 2 mg in a Treat-to-control Regimen (TALON)
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- Novartis Pharmaceuticals
- Study ID
- NCT04005352
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 50 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Brolucizumab 6 mg — BIOLOGICALIntra-vitreal injection
- Aflibercept 2 mg — BIOLOGICALIntra-vitreal injection
Study Details
This was a 64-week randomized, double-masked, multi-center, active-controlled, two-arm study in patients with neovascular age related macular degeneration (nAMD) who have not previously received anti- vascular endothelial growth factor (VEGF) treatment.
Key Dates
- Start date
- Sep 25, 2019
- Status verified
- Oct 2024
- Primary completion
- Sep 9, 2022
- Completion
- Sep 9, 2022
Study Design
- Enrollment
- 734 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Brolucizumab 6 mg3 x 4-week injections and one 8-week Intra-vitreal injection, followed by Treat-to- Control treatment from Week 16 up to Week 60/62.
- Active Comparator: Aflibercept 2 mg3 x 4-week injections and one 8-week Intra-vitreal injection, followed by Treat-to- Control treatment from Week 16 up to Week 60/62
Primary Outcome Measure
Distribution of the Last Interval With no Disease Activity up to Week 32 - Study Eye [ Time Frame: Up to Week 32 ]
Locations (24)
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