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Using panitumumab with ranibizumab injected into the eye to treat exudative age-related macular degeneration

Intravitreal panitumumab combined with intravitreal ranibizumab for exudative age-related macular degeneration

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN85022211
Enrollment
200
Registered
2023-12-20
Start date
2023-12-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Exudative age-related macular degeneration Eye Diseases

Interventions

This is a 2-year, prospective, randomized, double-masked, controlled study of the safety and efficacy of repeated intravitreal injections of panitumumab combined with intravitreal injections of ranibi

Sponsors

Ufa Eye Research Institute
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Best corrected visual acuity of 300µm 3. Normal intraocular pressure 4. Transparent optical media 5. Absence of any other eye disease (except for cataract or pseudophakia) 6. No previous retinal or vitreoretinal surgery (except for peripheral retinal argon laser coagulation)

Exclusion criteria

Exclusion criteria: 1. Inability to attend the follow-up examinations 2. Inability to understand the purpose and structure of the study.

Design outcomes

Primary

MeasureTime frame
1. Change in the retinal thickness in the foveola, as measured from Bruch´s membrane to the inner limiting membrane (i.e., including the retinal pigment epithelium layer), measured using optical coherence tomography (OCT) of the macula and optic nerve head at the time of the injections/re-injections 2. Best Corrected Visual Acuity (BCVA) measured using eye chart (ETDRS chart) at the time of the injections/re-injections

Secondary

MeasureTime frame
At baseline, at the time of the injections and re-injections, and at study end using optical coherence tomography: 1. Area and volume of subretinal tissue (differentiated between the compartment above and beneath the RPE line), and macular intraretinal and subretinal edema. 2. Size of atrophic lesions (geographic atrophies)

Countries

Russian Federation

Contacts

Public ContactJost Jonas
Jost.Jonas@medma.uni-heidelberg.de+49 6221 3929320

Outcome results

None listed

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