SHR-1314 clinical trials
SHR-1314 is named as an intervention in 3 current clinical trials in our China register. 1 is recruiting patients now. All registered phases are Phase 3. The lead sponsor is Suzhou Suncadia Biopharmaceuticals Co., Ltd. The most-studied condition is Active Non-radiographic Axial Spondyloarthritis.
Patient leaflets for SHR-1314
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 SHR-1314
3 trials| Study | Phase | Status | Lead sponsor | Registers |
|---|---|---|---|---|
|
A Trial of SHR-1314 Injection in Adult Patients With Active Non-radiographic Axial Spondyloarthritis
NCT06860750 · ClinicalTrials.gov ↗ · Active Non-radiographic Axial Spondyloarthritis
|
Phase 3 | Recruiting | Suzhou Suncadia Biopharmaceuticals Co., Ltd | China |
|
The Efficacy and Safety of SHR-1314 in the Treatment of Pediatric Patients of Age 6 to <18 Years With Moderate to Severe Plaque Psoriasis
NCT06833307 · ClinicalTrials.gov ↗ · Children and Adolescents Aged 6 to 18 With Moderate-to-Severe Plaque Psoriasis
|
Phase 3 | Not yet open | Suzhou Suncadia Biopharmaceuticals Co., Ltd | China |
|
A Study of the Efficacy and Safety of SHR-1314 for Adult Active Psoriatic Arthritis
NCT06640257 · ClinicalTrials.gov ↗ · Psoriatic Arthritis
|
Phase 3 | Active, closed | Suzhou Suncadia Biopharmaceuticals Co., Ltd | 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 SHR-1314
3 conditionsSponsors
lead sponsor per trial| Lead sponsor | Trials |
|---|---|
| Suzhou Suncadia Biopharmaceuticals Co., Ltd | 3 |
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.
Questions about SHR-1314 trials
How many clinical trials are testing SHR-1314?
3 current trials in our China register name SHR-1314 as a drug or biological intervention, as of the registry sync on 9 November 2026. Completed and withdrawn studies are not counted.
Are SHR-1314 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 SHR-1314 clinical trials?
The lead sponsor is Suzhou Suncadia Biopharmaceuticals Co., Ltd. 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 SHR-1314 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 SHR-1314 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 SHR-1314 (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.