RMP-A03 Ocular Suspension in Patients With Pterygium

Status Active, not recruiting

Clinical Trial Summary

The goal of this clinical trial is to test the safety and efficacy of an ocular medication on the treatment of pterygium.

Clinical Trial Description

Following informed consent, patients with pterygium who meet all eligibility criteria will be randomized to an 84-day double-blinded study to measure the safety and efficacy of the study drug as compared to placebo. ;

Study Design

Related Conditions & MeSH terms

Pterygium

Clinical Trial Details

NCT number	NCT05794204
Study type	Interventional
Source	Suzhou Raymon Pharmaceuticals Company, Ltd.
Contact
Status	Active, not recruiting
Phase	Phase 2
Start date	June 9, 2023
Completion date	July 2024

View Details

See also
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Completed	`NCT00346450` - Autologous ex Vivo Conjunctival Epithelial Cell Expansion for Ocular Surface Transplantation	Phase 3
Completed	`NCT03533244` - A Study of the Response to AG-86893 in Patients With Pterygium Hyperemia	Phase 2
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Unknown status	`NCT02015000` - Surgical Result of Pterygium Extended Removal Followed by Fibrin Glue Assisted Amniotic Membrane Transplantation	N/A
Completed	`NCT00344201` - Assessment of Fibrin Glue in Pterygium Surgery and Other Forms of External Eye Surgery	Phase 1
Recruiting	`NCT00326560` - Comparison of Glue With Sutures for Pterygium Surgery	Phase 3