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Trial registered on ANZCTR
Registration number
ACTRN12624000971538
Ethics application status
Approved
Date submitted
10/07/2024
Date registered
9/08/2024
Date last updated
29/09/2024
Date data sharing statement initially provided
9/08/2024
Type of registration
Prospectively registered
Titles & IDs
Public title
A Phase II, Multicentre, 2-part, Study of the Safety, Tolerability, and Efficacy of Intravitreal Fludrocortisone Acetate in Subjects with Geographic Atrophy Secondary to Age-related Macular Degeneration
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Scientific title
A Phase II, Multicentre, 2-part, Study of the Safety, Tolerability, and Efficacy of Intravitreal Fludrocortisone Acetate in Subjects with Geographic Atrophy Secondary to Age-related Macular Degeneration
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Secondary ID [1]
312359
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None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Geographic atrophy (GA) secondary to age-related macular degeneration (AMD)
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Condition category
Condition code
Eye
330816
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0
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Diseases / disorders of the eye
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Part A: An open label non randomised evaluation of the safety and tolerability of multiple doses of intravitreal (IVT) fludrocortisone acetate (FCA) in 9 subjects over 28 weeks of participation. Following screening, the schedule of activities includes attendance on Day 1, then Weeks 4, 8, 12, 16, 20, 24 and 28 for safety assessments.
Assessments vary depending upon the visit schedule and will include; evaluation of nature, frequency, and severity of adverse events (AEs)/ serious adverse events (SAEs), including relationship to study intervention, AEs leading to study intervention discontinuation or study discontinuation, assessments of adverse event of special interest (AESI), which includes endophthalmitis, retinal detachment, traumatic cataract, and increased intraocular pressure (IOP), ophthalmic examinations (slit lamp biomicroscopy, dilated ophthalmoscopy) and imaging assessment (spectral domain optical coherence tomography [SD-OCT], colour fundus photography [CFP], fundus fluorescein angiography [FFA]), changes in haematology and clinical chemistry laboratory parameters, routine urinalysis, vital signs (blood pressure, pulse rate, and temperature), and physical examination. Each visit will take between 1 and 2 hours.
Participants will receive two doses of FCA 2 mg/0.1 mL to one eye (study eye). The first on Day 1 and the second in Week 12, both doses will be administered by an ophthalmologist.
Only one eye will be selected as the study eye. If both eyes are eligible, the eye with worse visual acuity (VA) and/or visual function will be chosen as the study eye. If both eyes have the same visual function, the eye with the larger geographic atrophy (GA) area will be considered as the study eye.
Intervention adherence will be documented on investigational product (IP) dispensing and administration logs. Study participation time is up to 32 weeks from screening to end of study.
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Intervention code [1]
328857
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Treatment: Drugs
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Comparator / control treatment
Part A: No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Part A: To evaluate the safety and tolerability of multiple doses of IVT FCA injections in subjects with early GA secondary to AMD.
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Assessment method [1]
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Safety and tolerability will be assessed as a composite primary outcome. Assessments include evaluation of nature, frequency, and severity of AEs / SAEs, including relationship to study intervention, AEs leading to study intervention discontinuation or study discontinuation, assessments of AESI, which includes endophthalmitis, retinal detachment, traumatic cataract, and increased IOP, ophthalmic examinations (slit lamp biomicroscopy, dilated ophthalmoscopy) and imaging assessment SD-OCT, CFP, FFA, changes in haematology and clinical chemistry laboratory parameters, routine urinalysis, vital signs (blood pressure, pulse rate, and temperature), and physical examination.
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Timepoint [1]
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Day 1 (injection day) and weeks 4, 8, 12, 16, 20, 24 and 28, post injection or early discontinuation (ED), or as required.
-AEs, full and abbreviated (as required based on symptoms) physical examination, vital signs, IOP, ophthalmic examinations, and ophthalmic imaging.
Screening, then Day 1 (injection day) and weeks 12 and 28 post injection or ED or as required,
-Urine pregnancy test.
Day 1 (injection day) and weeks 12, and 28 post injection, or ED, or as required.
- CFP plus anterior segment
Screening, then Week 12 and 24 post injection or as required
-Urinalysis
Screening, then Week 12 and 28 post injection or ED, or as required
- Haematology and clinical chemistry
Screening then Week 12 post injection
- FFA
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Secondary outcome [1]
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Not applicable
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Assessment method [1]
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Not applicable
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Timepoint [1]
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Not applicable
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Eligibility
Key inclusion criteria
1. The subject must voluntarily sign and date an informed consent, approved by the HREC, prior to the initiation of any screening or study-specific procedures. A legally authorised representative may be used in case the subject is unable to read due to literacy.
2. In the opinion of the Investigator, willing and able to follow study instructions and likely to complete all scheduled study visits.
3. Male or female subjects.
4. Subjects aged 50 years and over.
5. Female subjects must be of nonchildbearing potential or show a negative pregnancy test at screening and must agree to use appropriate methods of contraception during the study.
6. Males with female partners of childbearing potential must agree to use appropriate methods of contraception and agree to refrain from donating sperm during the study.
7. BCVA of 30 letters or better using Early Treatment Diabetic Retinopathy Study (ETDRS) charts (20/200 Snellen equivalent).
8. Diagnosis of GA secondary to AMD, confirmed using FAF within 28 days prior to randomisation, to the following criteria:
a. GA defined as a sharply delineated, roughly round or oval area of partial or complete retinal pigment epithelium (RPE) depigmentation, resulting in better visibility of the underlying large choroidal vessels
b. Total GA area must be greater than or equal to 1.25mm2 and less than or equal to 17.5 mm2
- If GA is multifocal, at least one focal lesion must be greater than or equal to 1.25mm2
c. The GA lesion/s must be completely visualised on the macula centred image, able to be imaged in its entirety, and must be able to be measured separately from any areas of peripapillary atrophy
d. Presence of any pattern of hyper-autofluorescence in the junctional zone of GA.
9. Sufficiently clear ocular media, adequate pupillary dilation, fixation to permit quality fundus imaging, and ability to cooperate for adequate visual function testing and anatomic assessment in the study eye.
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Minimum age
50
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
1. GA due to causes other than AMD such as Stargardt disease, cone rod dystrophy, or toxic maculopathies like plaquenil maculopathy.
2. Spherical equivalent refractive error of -6.00 diopters of myopia or worse, or an axial length greater than 26 mm.
3. Any history, or current evidence of exudative (“wet”) AMD; including any evidence of RPE rips or evidence of neovascularisation anywhere in the retina.
4. Retinal disease other than AMD; however, benign conditions of the vitreous or peripheral retina are not exclusionary (ie, pavingstone degeneration).
5. Any ophthalmologic condition that reduces the clarity of the media and that, in the opinion of the Investigator, interferes with ophthalmologic examination and/or prevents adequate imaging of the retina (e.g. advanced cataract or corneal abnormalities).
6. Intraocular surgery (including lens replacement surgery) within 3 months prior to randomisation.
7. Aphakia or absence of the posterior capsule
- Previous violation of the posterior capsule is also excluded unless it occurred as a result of yttrium aluminium garnet (YAG) laser posterior capsulotomy in association with prior posterior chamber intraocular lens implantation and at least 60 days prior to Day 1.
8. Any ophthalmic condition that may require surgery during the study period.
9. Any contraindication to IVT injection including current ocular or periocular infection in either eye.
10. History of uveitis or endophthalmitis in either eye.
11. Current uncontrolled intraocular pressure (determined by the Investigator) or history of ocular hypertension or glaucoma.
12. Presence of iris neovascularisation and/or vitreous or preretinal haemorrhage.
13. Prior vitrectomy, glaucoma filtration surgery, or any ocular procedure which could affect drug distribution or clearance.
14. Ocular trauma to the eye within the preceding 6 months.
15. Participation in another interventional clinical study, or use of any experimental treatment for AMD or any other investigational product within 6 weeks or 5 half-lives (whichever is longer) prior to the start of study treatment. Clinical trials solely involving observation, over-the-counter vitamins, supplements, or diets are not exclusionary.
16. Systemic conditions which may contraindicate the use of mineralocorticoids, e.g. tuberculosis, uncontrolled hypertension, hypothyroidism, Cushing’s syndrome, hypokalaemia, myasthenia gravis, fungal infections, chronic heart failure, kidney disease with reduction in kidney function and fluid retention in the legs, or feet, or arms, or hands.
17. Medical or psychiatric conditions that, in the opinion of the Investigator, make consistent follow-up over the study period unlikely, or in general a poor medical risk because of other systemic diseases or active uncontrolled infections.
18. Screening laboratory value (haematology, serum chemistry, or urinalysis) that in the opinion of the Investigator is clinically significant and not suitable for study participation.
19. Hypersensitivity to fluorescein
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Part A: Allocation not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Phase 2
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
2/10/2024
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
9
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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EyeCo Pty Ltd
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Address [1]
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Country [1]
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
EyeCo Pty Ltd
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Address
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Bellberry Human Research Ethics Committee L
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Ethics committee address [1]
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123 Glen Osmond Road, Eastwood, Adelaide South Australia
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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16/07/2024
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Approval date [1]
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02/09/2024
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Ethics approval number [1]
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2024-07-896
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Summary
Brief summary
The study has two parts: A and B. The following information is for part A. Part A of this study will test if it is safe to give 2 doses of fludrocortisone (study drug) to people with geographic atrophy (GA), which is an advanced form of age-related macular degeneration (AMD) and explore the effectiveness of 2 doses on GA progression. Age-related macular degeneration is a disease of the macula, an area in the retina found at the back of the eye, needed for sharp, clear vision and activities such as reading and sewing. The advanced vision threating form of dry AMD is known as GA, which refers to a region of the retina where the cells wither away and die, creating patchy area in the retina. Sometimes, the patchy area looks like a map to the doctor who is examining the retina, hence the term “geographic atrophy.”
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Thomas Pham
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Address
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Sydney Retina Clinic and Day Surgery, Level 13, Park House, 187 Macquarie Street, Sydney, NSW 2000
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Country
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Australia
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Phone
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+61 2 80225838
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Dr Thomas Hong
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Address
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GreenLight Clinical, 134 William Street, Woolloomooloo NSW 2011
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Country
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Australia
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Phone
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+61 2 9191 0640
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Dr Thomas Hong
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Address
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GreenLight Clinical, 134 William Street, Woolloomooloo NSW 2011
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Country
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Australia
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Phone
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+61 2 9191 0640
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Fax
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Email
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
Deidentified overall patient data will be available or shared. Currently it is not planned to submit IPD, however should this change, this record will be updated
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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