Opthea’s OPT-302 granted FDA fast track designation for wet age-related macular degeneration

Opthea

6 July 2021 - FDA’s Fast Track Designation for OPT-302 offers benefits to expedite the OPT-302 Phase 3 clinical program and subsequent potential approval process.

Opthea is pleased to announce that the U.S. FDA has granted fast track designation for the company’s VEGF-C/-D ‘trap’ inhibitor, OPT-302, in combination with anti-VEGF- A therapy for the treatment of patients with neovascular (wet) age-related macular degeneration.

Read Opthea press release

Michael Wonder

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Michael Wonder

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Medicine , US , Fast track