Last reviewed · How we verify
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)
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 sponsor | Hoffmann-La Roche |
|---|---|
| Phase | PHASE3 |
| Status | RECRUITING |
| Enrolment | 68 |
| Start date | Mon Jun 17 2024 00:00:00 GMT+0000 (Coordinated Universal Time) |
| Completion | Thu Aug 30 2029 00:00:00 GMT+0000 (Coordinated Universal Time) |
Conditions
- Neovascular Age-related Macular Degeneration
- nAMD
Interventions
- PDS With Ranibizumab (100 mg/mL)
- Ranibizumab (10 mg/mL)
Countries
China