Skip to content

A multicenter, randomized controlled trial of advanced age-related macular degeneration

Multicenter, randomized controlled trial of active wAMD with fibrosis

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049055
Enrollment
Unknown
Registered
2021-07-20
Start date
2021-07-20
Completion date
Unknown
Last updated
2022-04-04

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

IBI302 treatment group:IBI302 treatment
EYLEA Group:Treatment of EYLEA

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. BCVA greater than 0.025 and less than or equal to 0.5, that is, greater than 1 letter number and less than or equal to 70 letter number (Snellen vision 20/40-20/800); 2. Patients secondary to WAMD with active fibrosis lesions and with fibrous scar area accounting for more than 50% of the whole lesion area; 3.3 No systemic or local anti-VEGF therapy or hormone therapy was given within a month; 4. The patient is younger than 80 years old and older than 50 years old.

Exclusion criteria

Exclusion criteria: 1. GA lesions or "atrophic fibrous lesions" progressing from AMD eyes: retinal thickness less than 100 microns; 2. The lesions that meet the relevant characteristics of OCT but lack the fundus characteristics of "clearly demarcated yellow-white raised tissue"; 3. Patients who have previously undergone intraocular surgery (such as vitrectomy) (excluding drug injection and cataract surgery for more than 3 months); 4. Poor refractive interstitial, poor general condition (hypertension greater than 160/100, glycation greater than 7.5%, coagulation disorder, etc.); 5. Other diseases involving the fundus and fovea, such as epimacular membrane, macular hole, RVO, etc.; 6. Patients with cardiovascular events within 6 months, tumor patients who need treatment, and patients with mental illness; 7. Those who are considered unsuitable by the researchers, such as psychological problems, disputes, economic problems, those who cannot understand communication, etc.

Design outcomes

Primary

MeasureTime frame
best corrected visual acuity;

Countries

China

Contacts

Public ContactSun Xiaodong

Shanghai General Hospital

xdsun@sjtu.edu.cn+86 13386259752

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026