Evidence map›Paper›PMID 38822444›Full record

ArticleEye and vision (London, England)2024

Efficacy of RCI001 as a therapeutic candidate of dry eye disease in a modified mixed dry eye model.

Young-Ho Jung, Young Ah Ku, Jayoon Moon, Seunghoon Kim, Jin Suk Ryu, Chang Ho Yoon, Myung Hee Chung, Yong Ho Kim, Mee Kum Kim, Dong Hyun Kim

Registry-linked trialAbstract read
In one paragraph

Article in Eye and vision (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07640867 (A Randomized, Double-Blind, Placebo-Controlled, Single- and Multiple-Administration Phase 1 Clinical Trial to Investigate the Pharmacokinetics, Safety, and Tolerability of RCI001 Eye Drops 0.25% in Healthy Male Subjects), which is not on this map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07640867 phase1completednot on this map

A Randomized, Double-Blind, Placebo-Controlled, Single- and Multiple-Administration Phase 1 Clinical Trial to Investigate the Pharmacokinetics, Safety, and Tolerability of RCI001 Eye Drops 0.25% in Healthy Male Subjects

TypeinterventionalSponsorRudacureRan2024 to 2025Enrolled40ConditionsDry EyeArmsRCI001 Eye Drops 0.25%, Placebo Eye Drops
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Young-Ho Jung *Department of Ophthalmology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Young Ah Ku *Department of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Jayoon MoonDepartment of Ophthalmology, Saevit Eye Hospital, Goyang, Republic of Korea.
Seunghoon KimDepartment of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Jin Suk RyuLaboratory of Ocular Regenerative Medicine and Immunology, Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.
Chang Ho YoonDepartment of Ophthalmology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Myung Hee ChungRudaCure Co., Ltd, Incheon, Republic of Korea.
Yong Ho KimDepartment of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea.
Mee Kum Kim *Department of Ophthalmology, Seoul National University College of Medicine, Seoul, Republic of Korea. kmk9@snu.ac.kr.
Dong Hyun Kim *Department of Pharmacology, Seoul National University College of Medicine, Seoul, Republic of Korea. amidfree@gmail.com.ORCID http://orcid.org/0000-0002-3985-990X

Funding

a grant of Korea University Anam Hospital K2319651 and K2225511National Research Foundation of Korea No. RS-2023-00243720
6 · The paper itself

Abstract

backgroundTo evaluate the therapeutic effects of topical RCI001 (RCI) and compare its efficacy with that of 1% prednisolone acetate (PDE) and 5% Lifitegrast in a modified mixed dry eye disease (DED) model.

methodsThe environmental DED model was induced in BALB/c mice in a dry chamber with scopolamine. The eyes of the mice were treated topically with phosphate buffered saline (PBS), PDE, Lifitegrast or RCI twice daily for 1 week. Ocular surface staining (OSS), tear secretion, inflammatory cytokines in the ocular surface and lacrimal gland, and immunofluorescence staining in the conjunctiva and cornea(CC) were assessed.

resultsThe RCI group demonstrated better improvement of OSS and tear secretion than the PBS group (OSS, PBS: 13.0 ± 1.6, RCI: 9.4 ± 3.0; tear secretion, PBS: 5.0 ± 0.4 mm, RCI: 7.0 ± 0.3 mm, each P < 0.001) and better clinical efficacy than PDE and Lifitegrast groups on Day 7 (improvement rate of OSS, RCI: 32.45%, Lifitegrast: 13.13%, PDE: 12.25%). The RCI group resulted in significantly lower expression of oxidative stress markers in the CC than the PBS group (4-HNE, NOX2, and NOX4 in the conjunctiva; NOX2 in the cornea, each P < 0.05). However, the PDE and Lifitegrast groups did not show significant differences compared with the PBS group. There were no significant differences of inflammatory cytokines in the ocular surface and lacrimal gland between all groups.

conclusionTopical RCI001 showed excellent therapeutic effects in environmental DED models by stimulating tear secretion, modulating oxidative stress and improving corneal epithelial healing compared to 1% PDE and 5% Lifitegrast.

Indexed as

Dry eye diseaseInflammationOxidative stressRCI001Therapeutics

Identifiers

PMID38822444
PMCPMC11143567

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Registered trials

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