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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT06683742




Registration number
NCT06683742
Ethics application status
Date submitted
8/11/2024
Date registered
12/11/2024
Date last updated
8/07/2025

Titles & IDs
Public title
A 2-year Study of EYP-1901 in Subjects With Wet Age Related Macular Degeneration (wAMD) (LUCIA) Primary Efficacy Will be Determined at Week 56
Scientific title
A 2-year Phase 3, Multicenter, Prospective, Randomized, Double-Masked, Parallel-Group Study of EYP-1901, a Tyrosine Kinase Inhibitor (TKI), Compared to Aflibercept in Subjects With Wet AMD
Secondary ID [1] 0 0
EYP-1901-302
Universal Trial Number (UTN)
Trial acronym
wAMD
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Wet Age Related Macular Degeneration 0 0
wAMD 0 0
Condition category
Condition code
Eye 0 0 0 0
Diseases / disorders of the eye

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - EYP-1901
Treatment: Drugs - Aflibercept (2.0 mg)

Experimental: EYP-1901 2686 µg - EYP-1901

Active comparator: Aflibercept -


Treatment: Drugs: EYP-1901
Intravitreal Injection

Treatment: Drugs: Aflibercept (2.0 mg)
Intravitreal Injection
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Average change in best corrected visual acuity (BCVA)
Timepoint [1] 0 0
Weeks 52 and 56
Secondary outcome [1] 0 0
Rate of injection burden
Timepoint [1] 0 0
Week 56
Secondary outcome [2] 0 0
Average change in best corrected visual acuity (BCVA)
Timepoint [2] 0 0
Week 96

Eligibility
Key inclusion criteria
* Previously treated or treatment naïve patients with a documented diagnosis of wAMD in the study eye, with onset of disease that began at any time prior to the Screening Visit.
* Best Corrected Visual Acuity (BCVA) by Early Treatment Diabetic Retinopathy Study (ETDRS) letter score between 78 to 35 letters (approximately 20/32 to 20/200 Snellen equivalent) in the study eye at the Screening Visit and on Baseline (Day 1).
* For previously-treated subjects, must have been treated with at least 2 anti-VEGF IVT injections (i.e., aflibercept 2 mg, aflibercept 8 mg, bevacizumab, ranibizumab, or faricimab) in the previous 6 months for wAMD per standard of care in the study eye prior to the Screening Visit.
Minimum age
50 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Subfoveal fibrosis, atrophy, or scarring in the center subfield.
* BCVA using ETDRS charts <20 letters (20/400 Snellen equivalent) in the fellow eye.

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 3
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
27/11/2024
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
1/10/2027
Actual
Sample size
Target
400
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
Eye Clinic Albury Wodonga - Albury
Recruitment hospital [2] 0 0
Cerulea - East Melbourne
Recruitment hospital [3] 0 0
Marsden Eye Specialists - Parramatta
Recruitment hospital [4] 0 0
Sydney Retina Clinic and Day Surgery - Sydney
Recruitment postcode(s) [1] 0 0
- Albury
Recruitment postcode(s) [2] 0 0
- East Melbourne
Recruitment postcode(s) [3] 0 0
- Parramatta
Recruitment postcode(s) [4] 0 0
- Sydney
Recruitment outside Australia
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Arizona
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California
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Colorado
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Connecticut
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Florida
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Illinois
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Indiana
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Kentucky
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Louisiana
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Maryland
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Massachusetts
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Michigan
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Missouri
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New Jersey
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New York
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North Carolina
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Oklahoma
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Oregon
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Pennsylvania
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South Carolina
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South Dakota
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Tennessee
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Texas
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Utah
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Virginia
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Washington
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Brazil
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Sao Paulo
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Czechia
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Náchod
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Czechia
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Praha
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Hungary
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Budapest
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Hungary
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Debrecen
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Hungary
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Pécs
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India
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Bengaluru
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India
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Kolkata
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India
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Madurai
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India
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Miraj
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Israel
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Be'er Ya'aqov
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Israel
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Haifa
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Israel
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Jerusalem
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Israel
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Kfar Saba
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Israel
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Petah Tikva
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Israel
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Rehovot
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Poland
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Bydgoszcz
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Poland
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Olsztyn

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
EyePoint Pharmaceuticals, Inc.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Ramiro Ribeiro, MD, PhD
Address 0 0
Country 0 0
Phone 0 0
833-393-7646
Fax 0 0
Email 0 0
[email protected]
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/NCT06683742