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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT03894020
Registration number
NCT03894020
Ethics application status
Date submitted
22/03/2019
Date registered
28/03/2019
Date last updated
23/10/2023
Titles & IDs
Public title
GTSCOPE - To Evaluate the Natural Progression of Dry Age-related Macular Degeneration (AMD)
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Scientific title
A Study of Disease Progression in Genetically Defined Subjects With Geographic Atrophy (GA) Secondary to Age-related Macular Degeneration (AMD)
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Secondary ID [1]
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CPPY988A12001
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Secondary ID [2]
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GTSCOPE
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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:
Dry Age-related Macular Degeneration
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Macular Degeneration
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Retinal Disease
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Retinal Degeneration
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Geographic Atrophy
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Macular Atrophy
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Condition category
Condition code
Eye
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Diseases / disorders of the eye
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Skin
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Other skin conditions
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Other
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Research that is not of generic health relevance and not applicable to specific health categories listed above
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Geographic Atrophy (GA)
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Assessment method [1]
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Change from baseline in area of Geographic Atrophy, as assessed by Fundus Auto Fluoresence measured in mm2
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Timepoint [1]
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Up to 96 weeks
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Primary outcome [2]
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Colour Fundus (CF)
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Assessment method [2]
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Change from baseline in Colour Fundus Photography measured in mm2
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Timepoint [2]
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Up to 96 weeks
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Primary outcome [3]
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Retinal Drusen Volume
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Assessment method [3]
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Change from baseline in retinal drusen volume measured in mm3
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Timepoint [3]
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Up to 96 weeks
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Primary outcome [4]
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Early Treatment Diabetic Retinopathy Study (ETDRS) Best Corrected Visual Acuity (BCVA)
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Assessment method [4]
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Change from baseline in ETDRS BCVA reading score
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Timepoint [4]
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Up to 96 weeks
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Primary outcome [5]
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Retinal sensitivity
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Assessment method [5]
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Change from baseline in retinal sensitivity as assessed by microperimetry
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Timepoint [5]
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Up to 96 weeks
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Primary outcome [6]
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Visual Functioning Questionnaire
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Assessment method [6]
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Change from baseline in National Eye Institute Visual Functioning Questionnaire 25-Items Version (NEI VFQ-25) Minimum Score (Best) = 29. Maximum score (Worst) = 149
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Timepoint [6]
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Up to 96 weeks
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Primary outcome [7]
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Medical Events of Interest (MEI)
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Assessment method [7]
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Change from baseline in percentage of Participants with MEI
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Timepoint [7]
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Up to 96 weeks
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Primary outcome [8]
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Monocular and Binocular Reading Performance
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Assessment method [8]
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Change in Monocular and Binocular Reading Performance measured in words/min
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Timepoint [8]
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Up to 96 weeks
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Eligibility
Key inclusion criteria
1. Adults with unilateral or bilateral Geographic Atrophy (GA) due to Age-related Macular Degeneration (AMD)
2. BCVA of 40 letters or better using ETDRS charts
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Minimum age
18
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. Evidence or history of neovascular Age-related Macular Degeneration (AMD) or diabetic retinopathy
2. Significant ocular or non-ocular disease that would impact the subject's ability to participate in the study
3. Participation in another research study involving an investigational product within the previous 4 weeks or 5 half-lives whichever is longer from the screening/baseline OR received a gene/cell therapy at any time previously
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
8/01/2019
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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
2/03/2024
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Actual
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Sample size
Target
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Accrual to date
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Final
83
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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The University of Melbourne - The Centre for Eye Research Australia (CERA) - East Melbourne
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Recruitment hospital [2]
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Lions Eye Institute (LEI) - Nedlands - Nedlands
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Recruitment postcode(s) [1]
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3002 - East Melbourne
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Recruitment postcode(s) [2]
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6009 - Nedlands
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Recruitment outside Australia
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United States of America
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Arizona
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California
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Florida
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Georgia
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Illinois
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Indiana
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Iowa
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Maryland
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Massachusetts
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Southampton
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Sunderland
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Gyroscope Therapeutics Limited
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Address
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Other collaborator category [1]
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Commercial sector/industry
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Name [1]
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Novartis Pharmaceuticals
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Address [1]
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Ethics approval
Ethics application status
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Summary
Brief summary
An observational study to evaluate the natural progression of dry AMD in genetically defined subjects
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Trial website
https://clinicaltrials.gov/study/NCT03894020
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
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Contact person for scientific queries
No information has been provided regarding IPD availability
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/NCT03894020
Download to PDF