IBI302 clinical trials
IBI302 is named as an intervention in 3 current clinical trials in our China register. 1 is recruiting patients now. The most common phase is Phase 2. The sponsor with the most trials is Innovent Biologics Technology Limited (Shanghai R&D Center) (2). The most-studied condition is Neovascular Age-related Macular Degeneration.
Patient leaflets for IBI302
The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.
- UKUnited Kingdom: Search MHRA ProductsPatient information leaflets and SmPCs for UK-licensed products.
- USUnited States: Search DailyMedFDA-approved labels, including patient and medication guides.
Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.
Trials by status
Trials by phase
Clinical trials of IBI302
3 trials| Study | Phase | Status | Lead sponsor | Registers |
|---|---|---|---|---|
|
A Study to Evaluate the Efficacy and Safety of IBI302inSubjects With nAMD
NCT07275840 · ClinicalTrials.gov ↗ · Neovascular Age-related Macular Degeneration
|
Phase 2 | Recruiting | Innovent Biologics Technology Limited (Shanghai R&D Center) | China |
|
A Study to Evaluate the Efficacy and Safety of IBI302 in Subjects With nAMD
NCT05972473 · ClinicalTrials.gov ↗ · Neovascular Age-related Macular Degeneration
|
Phase 3 | Active, closed | Innovent Biologics (Suzhou) Co. Ltd | China |
|
A Study to Evaluate the Efficacy and Safety of IBI302 inSubjects With Diabetic Macular Edema（DME）
NCT06908876 · ClinicalTrials.gov ↗ · Diabetic Macular Oedema
|
Phase 2 | Active, closed | Innovent Biologics Technology Limited (Shanghai R&D Center) | China |
Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.
Conditions studied with IBI302
2 conditionsSponsors
lead sponsor per trial| Lead sponsor | Trials |
|---|---|
| Innovent Biologics Technology Limited (Shanghai R&D Center) | 2 |
| Innovent Biologics (Suzhou) Co. Ltd | 1 |
By country register
| Register | Trials | Recruiting |
|---|---|---|
| Clinical trials in China | 3 | 1 |
A trial with sites in more than one country appears in each of those registers.
Related compounds
Questions about IBI302 trials
How many clinical trials are testing IBI302?
3 current trials in our China register name IBI302 as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.
Are IBI302 trials recruiting patients?
Yes. 1 of the 3 trials is recruiting: 1 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.
Who sponsors IBI302 clinical trials?
Innovent Biologics Technology Limited (Shanghai R&D Center) (2) and Innovent Biologics (Suzhou) Co. Ltd (1). The number in brackets is how many trials each organisation leads.
Where does this information come from?
Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how IBI302 works or whether it is effective, and it is not medical advice.
How this page is built
Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how IBI302 works or whether it is effective. Each trial links to its own record so you can check it yourself.
- ClinicalTrials.gov (U.S. National Library of Medicine) ↗ Trial IDs, titles, intervention names and synonyms, phase, overall status, lead sponsor and conditions for every trial on this page
This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists IBI302 (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 9 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.