Skip to content

Analysis of genotypes associated with the treatment effects of Lucentis for age-related macular degeneration

Analysis of genotypes associated with the treatment effects of Lucentis for age-related macular degeneration - ANGEL study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005584
Enrollment
600
Registered
2011-05-16
Start date
2011-09-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

age-related macular degeneration

Interventions

Patients receive three monthly intravitreal injections of ranibiumab (0.5mg) and followed up monthly for 12 months. Repeat injections were given to patients who showed insufficient effects of treatmen

Sponsors

Kyoto University Graduate School of Medicine, Department of Ophthalmology and Visual Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Treatment naive active angiographically subfoveal choroidal neovascularization associated with age-ralated macular degeneration with best corrected visual acuity of 32/40 to 20/400

Exclusion criteria

Exclusion criteria: Previous treatment with photocoagulation, surgery, photodynamic therapy, Transpupillary thermotherapy, radiation Subfoveal fibrosis or atrophy History of vitrectomy Intraocular surgery within 2 months CNV in either eye due to other causes, such as ocular histo-plasmosis, trauma, or pathological myopia Aphakia or absence of the posterior capsule in the study eye unless it resulted from yttrium aluminum garnet (YAG) posterior capsulotomy in association with prior posterior chamber intraocular lens implantation.

Design outcomes

Primary

MeasureTime frame
visual acuity change at 12 months after the first treatment

Secondary

MeasureTime frame
disappearance of retinal exudative change at 3 months, visual acuity change at 3 months, interval for additional treatment, and number of treatment during 12 months

Countries

Japan

Contacts

Public ContactKenji Yamashiro

Kyoto University Graduate School of Medicine Department of Ophthalmology and Visual Sciences

yamashro@kuhp.kyoto-u.ac.jp075-751-3248

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026