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Ranibizumab (LUCENTIS®)

Phase 3
AbbVie Inc. (ABBV)

Phase 3

Development Phase

1

Upcoming Catalysts

0

Historical Events

1

Regulatory Approvals

Upcoming Catalysts
What are catalysts?
Dec '26
ABBVPhase 3

Ranibizumab (LUCENTIS®) Phase 3 Est. Readout

Ranibizumab (LUCENTIS®)
Dec 2026~
CT.gov
00%
Competitive Landscape

0 competitors in AMD

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Drug Information

Target Indication

AMD

Clinical Trial

NCT04704921

Last updated: 1/13/2026

Patent & Exclusivity

No patent data available. Pre-approval drugs may not have Orange Book listings.

Regulatory Approvals
EMA1/22/2007

Lucentis

Lucentis is indicated in adults for: The treatment of neovascular (wet) age-related macular degeneration (AMD) The treatment of visual impairment due to choroidal neovascularisation (CNV) The treatment of visual impairment due to diabetic macular oedema (DME) The treatment of visual impairment due to macular oedema secondary to retinal vein occlusion (branch RVO or central RVO)

View on EMA
Drug Science
Mechanism of action & safety profile
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