Japanese Phase 3 Study of Aflibercept in Neovascular Glaucoma Patients

PHASE3CompletedINTERVENTIONAL
Enrollment

54

Participants

Timeline

Start Date

April 2, 2015

Primary Completion Date

June 16, 2016

Study Completion Date

September 6, 2016

Conditions
Glaucoma, Neovascular
Interventions
DRUG

Aflibercept (Eylea, BAY 86-5321)

After the first aflibercept IVT injection on Day 1, subjects may receive sham injection at Week 1, and aflibercept injection at Week 5 and/or Week 9 if the re-treatment criteria are met.

DRUG

Sham Injection

After the first sham injection on Day 1, subjects may receive aflibercept IVT injection at Week 1, Week 5 and/or Week 9 if re-treatment criteria are met.

Trial Locations (19)

910-1193

Yoshida

501-1194

Gifu

660-8550

Amagasaki

671-1227

Himeji

650-0017

Kobe

920-8641

Kanazawa

216-8511

Kawasaki

980-8574

Sendai

879-5593

Yufu

573-1191

Hirakata

565-0871

Suita

569-8686

Takatsuki

693-8501

Izumo

113-8655

Bunkyo-ku

181-8611

Mitaka

755-8505

Ube

409-3898

Chūō

602-0841

Kyoto

545-8586

Osaka

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Regeneron Pharmaceuticals

INDUSTRY

lead

Bayer

INDUSTRY