Zenkuda and Tabirafusp-ted Meet Primary Endpoints in Pivotal DAYBREAK Trial in wAMD
Zenkuda Demonstrates a Potential New Standard-of-Care Profile with Strong Immediacy and Sustained Clinical Effect with Majority of Patients on 24-week Dosing Interval Using Strict Treat-to-Dryness Real World Retreatment Criteria
Phase 1 First-In-Human Study of KSI-301: A Novel Anti-VEGF Antibody Biopolymer Conjugate With Extended Durability Following a Single Dose Administration (3670)
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