Intravitreal Brolucizumab in Neovascular Age-related Macular Degeneration With Limited Response to Aflibercept

NCT ID: NCT04287348

Last Updated: 2021-12-29

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE4
• Total Enrollment: 16 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-07-20
• Study Completion Date: 2021-11-22

Brief Summary

The purpose of this investigator initiated study is to identify the effects of intravitreal brolucizumab on recurrence-free treatment intervals and morphological features in choroidal neovascularizations (CNV) due to age-related macular degeneration (AMD) in which the Optical coherence tomography (OCT) guided treatment interval failed to be extended to 6, 8 or 10 weeks intervals in a treat and extend regimen using aflibercept.

Detailed Description

Outcome Measures:

The primary outcome is the mean maximum treatment interval with intravitreal brolucizumab at month 6 and 12.

The secondary outcomes are:

• Best corrected visual acuity (BCVA) in letters and BCVA change (letters) from baseline (=switch to brolucizumab) to month 6 and 12.
• Number of brolucizumab intravitreal treatments applied during the 12 months study period.
• Central retinal thickness (CRT, in µm) as measured in the central ETDRS subfield Spectral-Domain Optical coherence tomography (SD-OCT) at baseline, month 6 and 12.
• Presence of qualitative SD-OCT features like intraretinal fluid, subretinal fluid, pigment epithelial detachment and hyperreflective foci at baseline, month 6 and 12.
• Total CNV area and vessel density as measured by OCTangiography (OCTA) at baseline, month 6 and 12.
• Total area of leakage from CNV and the total lesion area as evaluated by Fluorescein angiography (FA) at baseline and month 12.
• VFQ-25 total and subscores as evaluated by quality of life questionnaire VFQ-25 at baseline and month 6 and 12.
• Rates of adverse events and serious adverse events at 6 and 12 months.

Conditions

Neovascular Age-related Macular Degeneration

Keywords

AMD, poor responders, aflibercept, brolucizumab

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Beovu (Brolucizumab)

Prospective, one-treatment-arm, monocentre study

Group Type: OTHER

Brolucizumab 6 mg solution for intravitreal injection

Intervention Type: DRUG

All consenting, enrolled patients (irrespectively of maximum recurrence-free interval under aflibercept pretreatment) will receive an intravitreal injection of brolucizumab 6 mg at baseline (week 0), at week 4 and each of the following treat and extend visits. At each visit all patients will undergo an OCT assessment. For all patients extension of treatment intervals is only possible 2-week-stepwise, e.g. 4, 6, 8 weeks etc.

Interventions

Brolucizumab 6 mg solution for intravitreal injection

All consenting, enrolled patients (irrespectively of maximum recurrence-free interval under aflibercept pretreatment) will receive an intravitreal injection of brolucizumab 6 mg at baseline (week 0), at week 4 and each of the following treat and extend visits. At each visit all patients will undergo an OCT assessment. For all patients extension of treatment intervals is only possible 2-week-stepwise, e.g. 4, 6, 8 weeks etc.

Intervention Type: DRUG

Other Intervention Names

Beovu

Eligibility Criteria

Inclusion Criteria

• Male or female patients ≥ 50 years of age.
• Patients with active subfoveal or juxtafoveal Type 1, 2 or 3 CNV secondary to AMD.
• Pre-treatment with intravitreal aflibercept in a treat and extend regimen with 2-weeks steps and failing to be extended by two weeks to either 6-weeks intervals, 8 week intervals or 10 week intervals without showing CNV activity (at least 2 attempts to extend).
• The total area of CNV (including both classic and occult components) encompassed within the lesion must be ≥ 50% of the total lesion area.
• The total lesion area ≤ 12 disc areas for minimally classic or occult with no classic component and ≤ 9 disc areas (5400μm) in greatest linear dimension with predominantly classic lesions.
• Patients who have a BCVA of at least 20/160 (letter score 40 letters) in the study eye using ETDRS charts.
• Willing and able to give written informed consent according to legal requirements, and who have signed the consent form prior to initiation of any study procedure including withdrawal from exclusionary medications for the purpose of this study.
• Willing and able to comply with study procedures.

Exclusion Criteria

• Subretinal hemorrhage in the study eye that involves the center of the fovea, if the size of the hemorrhage is either ≥ 50% of the total lesion area or ≥ 1 disc area in size.
• Presence of a retinal pigment epithelial tear involving the fovea in the study eye.
• Patients with angioid streaks or precursors of CNV in either eye due to other causes, such as ocular histoplasmosis, trauma, or pathologic myopia.
• Concurrent disease in the study eye that could compromise visual acuity or require medical or surgical intervention during the 12 months study period.
• Vitreous hemorrhage or history of retinal detachment or macular hole (Stage 3 or 4) in the study eye.
• Active intraocular inflammation (grade trace or above) in the study eye.
• Any active infection involving ocular adnexa including infectious conjunctivitis, keratitis, scleritis, endophthalmitis, as well as idiopathic or autoimmune-associated uveitis in either eye.
• History of uncontrolled glaucoma in the study eye (defined as intraocular pressure ≥ 25 mmHg despite treatment with anti-glaucoma medication).
• Aphakia with absence of the posterior capsule in the study eye.
• Any prior treatment in the study eye with radiation therapy, subfoveal focal laser photocoagulation, vitrectomy, transpupillary thermotherapy.
• History of submacular surgery or other surgical intervention for AMD in the study eye, glaucoma filtration surgery, corneal transplant surgery.
• Extracapsular extraction of cataract with phacoemulsification within three months preceding Baseline, or a history of post-operative complications within the last 12 months preceding Baseline in the study eye (uveitis, cyclitis, etc.).
• Use of other investigational drugs at the time of baseline, or within 30 days or 5 half- lives of baseline, whichever is longer (excluding vitamins and minerals).
• Previous violation of the posterior capsule in the study eye unless it occurred as a result of YAG posterior capsulotomy in association with prior, posterior chamber intraocular lens implantation.
• History of other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use an investigational drug or that might affect interpretation of the results of the study or render the subject at high risk for treatment complications.
• Pregnant or nursing (lactating) women, where pregnancy is defined as the state of a female after conception and until the termination of gestation, confirmed by a positive hCG laboratory test (>5 mIU/ml).
• History of hypersensitivity or allergy to fluorescein.
• Inability to obtain OCTs, OCTAs, fundus photographs or fluorescein angiograms of sufficient quality.

• Minimum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Novartis

INDUSTRY

Sponsor Role: collaborator

Vista Klinik

OTHER

Sponsor Role: lead

Responsible Party

PD Dr. med. Katja Hatz

Head of Medical Retina and clinical Research department

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Katja Hatz, PD Dr. med

Role: PRINCIPAL_INVESTIGATOR

Vista Klinik Binningen

Locations

Vista Klinik

Binningen, Basel-Landschaft, Switzerland

Countries

Switzerland

Other Identifiers

ROBIN / CRTH258ACH01T

Identifier Type: -

Identifier Source: org_study_id