Viewing Study NCT05794204


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Ignite Modification Date: 2025-12-26 @ 5:13 PM
Study NCT ID: NCT05794204
Status: COMPLETED
Last Update Posted: 2024-12-06
First Post: 2023-03-20
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: RMP-A03 Ocular Suspension in Patients With Pterygium
Sponsor: Suzhou Raymon Pharmaceuticals Company, Ltd.
Organization:

Study Overview

Official Title: A Phase 2a Study Evaluating the Safety and Efficacy of RMP-A03 Ocular Suspension in Patients With Pterygium
Status: COMPLETED
Status Verified Date: 2024-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to test the safety and efficacy of an ocular medication on the treatment of pterygium.
Detailed 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 Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: