NCT05712720

Study to Evaluate the Efficacy and Safety of RZ402 in Diabetic Macular Edema (DME)

A Randomized, Double-Masked, Placebo-Controlled, Parallel-Arm Study to Evaluate the Efficacy and Safety of RZ402 in Participants With Diabetic Macular Edema (DME)
Rezolute·Phase 2·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Diabetic Macular Edema
Drug/Device/Intervention
Experimental: Group 1
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Rezolute
Location
Phoenix,Beverly Hills,Fullerton,Modesto,Santa Barbara,Coral Springs,Winter Haven,Augusta,Oak Forest,Hagerstown,Royal Oak,Saint Louis Park,Saint Louis,Reno,Bloomfield,Great Neck,New York,Springfield,La, United States of America
Timeline & enrollment
Phase
Phase 2
Start date
Feb 06, 2023
End date
Jan 01, 2024
Enrollment
100 participants
Primary outcome

Safety Events,Change in Central Subfield Thickness

Summary

The objective of this trial is to assess the safety, efficacy, and tolerability of RZ402 in
 patients with Diabetic Macular Edema.

ICD-10 classifications
Diabetic retinopathyOther specified diabetes mellitus with ophthalmic complicationsUnspecified diabetes mellitus with ophthalmic complicationsDiabetic cataractType 2 diabetes mellitus with ophthalmic complications
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT05712720
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT05712720 through Pure Global AI's free database. This Phase 2 trial is sponsored by Rezolute and is currently Recruiting. The study focuses on Diabetic Macular Edema. Target enrollment is 100 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.