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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT03604328
Registration number
NCT03604328
Ethics application status
Date submitted
10/07/2018
Date registered
27/07/2018
Titles & IDs
Public title
Safety and Tolerability of a Prostaglandin Ocular Implant for Treatment of Open Angle Glaucoma
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Scientific title
An Open-label Phase I Study to Evaluate the Safety, Tolerability and Biodegradation Period of PolyActiva PA5108 Ocular Implant When Administered Intracamerally to the Anterior Chamber of the Eye
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Secondary ID [1]
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LATA-CS101
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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:
Open-angle Glaucoma
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Condition category
Condition code
Eye
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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
Treatment: Drugs - PA5108
Experimental: PA5108 - PA5108 ocular implant (study eye) and topical prostaglandin analogue therapy (non-study eye)
Treatment: Drugs: PA5108
single ocular implant, administered on day 1
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Intervention code [1]
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Treatment: Drugs
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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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Safety and tolerability as measured by the occurrence of adverse events
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Assessment method [1]
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Timepoint [1]
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4 weeks
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Secondary outcome [1]
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Timeframe to complete implant biodegradation based on implant size and location
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Assessment method [1]
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Timepoint [1]
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6 months
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Eligibility
Key inclusion criteria
* Grade 3 or 4 open angle glaucoma (Shaffer-Etienne scale)
* Visual acuity in non-study eye same or better than study eye
* Currently taking topical ocular hypotensive medication including a prostaglandin analogue
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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
* Aphakic eyes
* Only one eye
* History of, or current uveitis, Cystoid Macular Edema (CME) or cornea edema
* Intraocular surgery or cornea/refractive surgery in study eye in past 6 months or anticipate need for eye surgery (including laser) in study eye during study period
* Current retinal detachment
* Uncontrolled infection in the eye
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Study design
Purpose of the study
Treatment
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Allocation to intervention
NA
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
Phase 1
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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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
24/07/2018
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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
15/06/2020
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Sample size
Target
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Accrual to date
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Final
8
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
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Centre for Eye Research Australia - East Melbourne
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Recruitment hospital [2]
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Melbourne Eye Specialists - Melbourne
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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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3000 - Melbourne
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
PolyActiva Pty Ltd
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
A single centre, open label, study to assess the safety, tolerability and biodegradation of PA5108 ocular implant in adults who have Open Angle Glaucoma (Primary or Secondary).
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Trial website
https://clinicaltrials.gov/study/NCT03604328
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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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Nathan Kerr
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Address
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The Royal Victorian Eye & Ear Hospital
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for scientific queries
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
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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/NCT03604328