A Study to Evaluate the Efficacy and Safety of IBI302 inSubjects With Diabetic Macular Edema(DME)

PHASE2RecruitingINTERVENTIONAL
Enrollment

150

Participants

Timeline

Start Date

April 24, 2025

Primary Completion Date

December 31, 2026

Study Completion Date

February 28, 2027

Conditions
Diabetic Macular Oedema
Interventions
BIOLOGICAL

IBI302

4 mg IBI302 will be administered by intravitreal injection into the study eye once every 4 weeks for 3 consecutive months, followed by Pro re nata (PRN) regimen.

BIOLOGICAL

IBI302

8 mg IBI302 will be administered by intravitreal injection into the study eye once every 4 weeks for 3 consecutive months, followed by PRN regimen.

DRUG

Faricimab

6 mg faricimab will be administered by intravitreal injection into the study eye once every 4 weeks for 4 consecutive months, followed by PRN regimen.

Trial Locations (1)

200080

RECRUITING

Shanghai General hospital, Shanghai

All Listed Sponsors
lead

Innovent Biologics Technology Limited (Shanghai R&D Center)

INDUSTRY

NCT06908876 - A Study to Evaluate the Efficacy and Safety of IBI302 inSubjects With Diabetic Macular Edema(DME) | Biotech Hunter | Biotech Hunter