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A Study of the Efficacy, Safety, and Pharmacokinetics (PK) of the Port Delivery System With Ranibizumab (PDS) in Chinese Participants With Neovascular Age-related Macular Degeneration (nAMD) (HUTONG)

NCT05562947 PHASE3 RECRUITING

This study will evaluate the efficacy, safety, and PK of ranibizumab 100 milligrams per milliliter (mg/mL) delivered every 24 weeks (Q24W) via the PDS implant compared with ranibizumab 0.5 milligrams (mg) delivered every 4 weeks (Q4W) as intravitreal (IVT) injection in chinese participants with nAMD.

Details

Lead sponsorHoffmann-La Roche
PhasePHASE3
StatusRECRUITING
Enrolment68
Start dateMon Jun 17 2024 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionThu Aug 30 2029 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

China