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NCT07275840

A Study to Evaluate the Efficacy and Safety of IBI302inSubjects With nAMD

Recruiting now Phase 2 Last updated 8 January 2026
What this trial tests

Phase 2 trial testing IBI302 8mg dose in Neovascular Age-related Macular Degeneration in 800 participants. Currently enrolling.

Timeline
5 December 2025
Primary endpoint
30 August 2026
30 August 2026

Quick facts

Lead sponsorInnovent Biologics Technology Limited (Shanghai R&D Center)
PhasePhase 2
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment800
Start date5 December 2025
Primary completion30 August 2026
Estimated completion30 August 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Innovent Biologics Technology Limited (Shanghai R&D Center) — full company profile →

Who can join

50 and older, any sex, with Neovascular Age-related Macular Degeneration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is designed for Open-label, multi-center, single-arm Phase II trail to evaluate the efficacy and safety of intravitreal injection of IBI302 in nAMD patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other recruiting trials for Neovascular Age-related Macular Degeneration

Currently open trials in the same condition.

Other Innovent Biologics Technology Limited (Shanghai R&D Center) trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07275840.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing