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The purpose of this study is to evaluate the safety and efficacy of GP-asPNA for in vivo treatment of severe antibiotic resistant bacterial keratitis.
This is a study of antisense oligonucleotides (ASOs) in adult (ages 18 to 70) participants with severe antibiotic resistant bacterial keratitis. Approximately 20 participants will be enrolled. Infectious keratitis or endophthalmitis, mainly caused by the trauma or intraocular surgical operation, has posed a grave threat to human vision health. Among them, infectious keratitis is the most common blinding keratopathy in developing countries. We develop a novel kind of Trojan strategy to specifically deliver ASOs into diverse bacteria rather than mammalian cells through the bacterial-specific ATP-binding cassette (ABC) sugar transporter. Compared with their cell-penetrating peptide counterparts, the antisense peptide nucleic acid modified with glucose polymer can be selectively internalized into human-derived multidrug- resistant Escherichia coli and methicillin-resistant Staphylococcus aureus, and they display a much higher uptake rate. The follow-up period was 90 days, and the patients will be followed up 1 days, 3±1 days, 7±1 days, 14±2 days, 30±2 days, and 90±5 days after treatment.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Eye & ENT Hospital of Fudan University
Shanghai, Shanghai Municipality, China
Start Date
October 11, 2023
Primary Completion Date
October 1, 2024
Completion Date
October 31, 2026
Last Updated
June 11, 2024
20
ESTIMATED participants
ASO
DRUG
Lead Sponsor
Eye & ENT Hospital of Fudan University
Collaborators
NCT06427317
NCT02177721
Data Source & Attribution
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