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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT06571045




Registration number
NCT06571045
Ethics application status
Date submitted
20/08/2024
Date registered
26/08/2024

Titles & IDs
Public title
A Study to Evaluate the Efficacy and Safety of 2 Doses of EYE103 Compared With Ranibizumab (0.5 mg) in Participants With DME
Scientific title
A Randomized, Double-Masked, Multi-Center, 3-Arm Pivotal Phase 2/3 Study to Evaluate The Efficacy and Safety of Intravitreal EYE103 Compared With Intravitreal Ranibizumab (0.5mg) in Participants With Diabetic Macular Edema
Secondary ID [1] 0 0
EYE-RES-102
Universal Trial Number (UTN)
Trial acronym
BRUNELLO
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Diabetic Macular Edema (DME) 0 0
Condition category
Condition code
Eye 0 0 0 0
Diseases / disorders of the eye
Cardiovascular 0 0 0 0
Diseases of the vasculature and circulation including the lymphatic system

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Ranibizumab
Treatment: Drugs - EYE103

Experimental: EYE103 Low Dose Treatment Arm - EYE103 Low Dose Treatment Arm

Experimental: EYE103 High Dose Treatment Arm - EYE103 High Dose Treatment Arm

Active comparator: Ranibizumab Treatment Arm - Ranibizumab Treatment Arm


Treatment: Drugs: Ranibizumab
Ranibizumab is a commercially available anti-VEGF treatment formulated for intravitreal administration for use in patients with diabetic macular edema

Treatment: Drugs: EYE103
EYE103 is a humanized antibody formulated for intravitreal administration
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Change from baseline Best-Corrected Visual Acuity measured using the standardized ETDRS chart
Assessment method [1] 0 0
Change from baseline Best-Corrected Visual Acuity measured using the standardized ETDRS chart
Timepoint [1] 0 0
52 Weeks
Secondary outcome [1] 0 0
Changes in structural and visual outcomes
Assessment method [1] 0 0
Changes in structural and visual outcomes
Timepoint [1] 0 0
Duration of the study, through Week 104

Eligibility
Key inclusion criteria
* Be willing and able to understand the study procedures and the risks involved and provide written informed consent before the first study-related activity
* Be male or female =18 years of age.
* Have type 1 or type 2 diabetes mellitus and a HbA1c of =12%.
* Have a decrease in vision in the study eye determined by the investigator to be primarily the result of DME.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Be pregnant or breastfeeding
* History of cataract surgery and/or minimally invasive glaucoma surgery in the study eye within 90 days of Screening
* Have any treatment for complications of cataract surgery with steroids or yttrium aluminum garnet (YAG) laser capsulotomy within 90 days of Screening
* Are currently using drugs with known retinal toxicity (e.g., Hydroxychloroquine, pentosan polysulfate sodium, and amiodarone)
* If treatment-experienced for DME have a history of any of the following treatments within the noted time windows:

* Have had prior treatment with 8 mg aflibercept (EYLEA HD) or faricimab (VABYSMO) within 120 days prior to the Screening visit in the study eye
* Have had an IVT with other anti-VEGF treatments (ranibizumab, bevacizumab, aflibercept [2 mg], brolucizumab, pegaptanib sodium) in the study eye within 90 days of the Screening visit

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 2
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
7/08/2024
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
31/12/2027
Actual
Sample size
Target
960
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
NSW
Recruitment hospital [1] 0 0
Sydney Retina Clinic - Sydney
Recruitment hospital [2] 0 0
Sydney, Australia - Sydney
Recruitment hospital [3] 0 0
Albury, Australia - Albury
Recruitment hospital [4] 0 0
Parramatta, Australia - Parramatta
Recruitment postcode(s) [1] 0 0
2000 - Sydney
Recruitment postcode(s) [2] 0 0
2135 - Sydney
Recruitment postcode(s) [3] 0 0
2640 - Albury
Recruitment postcode(s) [4] 0 0
2150 - Parramatta
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Arizona
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Maine
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Wolverhampton

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
EyeBiotech Ltd.
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Public notes

Contacts
Principal investigator
Name 0 0
Charles Miller, MD PhD
Address 0 0
EyeBiotech Ltd.
Country 0 0
Phone 0 0
Email 0 0
Contact person for public queries
Name 0 0
Charles Miller, MD PhD
Address 0 0
Country 0 0
Phone 0 0
212-914-0127
Email 0 0
ClinicalInquiries@eyebiotech.com
Contact person for scientific queries

Data sharing statement


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT06571045