Ireland
--:--IST
Priya Life Science Compound trial record
Compound · clinical trials

Stapokibart clinical trials

Also listed in trial records as CM310, Kangyueda
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 11 trials in our China and Japan registers that name Stapokibart as an intervention. Synced 10 Nov 2026
11Current trials
3Recruiting now
5Lead sponsors
2Country registers
At a glance

Stapokibart is named as an intervention in 11 current clinical trials in our China and Japan registers. 3 are recruiting patients now. The most common phase is Observational. The sponsor with the most trials is Chengdu Kangnuoxing Biopharma,Inc (6). The most-studied condition is Seasonal Allergic Rhinitis (SAR).

How Stapokibart works

All drug targets →
  • Antagonist at IL4R Primary target
    Target: IL4R interleukin 4 receptor
    Guide to Pharmacology only
Other medicines acting on IL4R
Diseases it has been tested for in clinical trials, by furthest phase
  • Atopic eczemaPhase 3
  • Bullous pemphigoidPhase 3
  • Chronic rhinosinusitis with nasal polypsPhase 3
  • Prurigo nodularisPhase 3
  • Seasonal allergic rhinitisPhase 3
  • Chronic obstructive pulmonary diseasePhase 2/3
  • PruritusPhase 2
  • Allergic rhinitisPhase 2
  • AsthmaPhase 2
  • Head and neck squamous cell carcinomaPhase 1

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL5095324, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 13785, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

Patient leaflets for Stapokibart

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-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

  • Recruiting327%
  • Not yet open655%
  • Active, closed218%

Trials by phase

  • Observational327%
  • Phase 3327%
  • Not applicable218%
  • Phase 219%
  • Phase 419%
  • Phase 2/319%
01

Clinical trials of Stapokibart

11 trials
StudyPhaseStatusLead sponsorRegisters
Study on the Treatment of Adolescent Patients With Seasonal Allergic Rhinitis
NCT07678931 · ClinicalTrials.gov ↗ · Seasonal Allergic Rhinitis (SAR)
Phase 3 Recruiting Chengdu Kangnuoxing Biopharma,Inc China, Japan
A Study of CM310 in Subjects With Moderate to Severe Asthma
NCT05761028 · ClinicalTrials.gov ↗ · Moderate to Severe Asthma
Phase 2/3 Recruiting CSPC ZhongQi Pharmaceutical Technology Co., Ltd China, Japan
A Study of Stapokibart Injection in Patients With Atopic Dermatitis (AD)
NCT07544862 · ClinicalTrials.gov ↗ · Atopic Dermatitis (AD)
Observational Recruiting Chengdu Kangnuoxing Biopharma,Inc China
A Cohort Study on Biomarkers to Predict the Efficacy of Biologics for Chronic Rhinosinusitis with Nasal Polyps
NCT06801353 · ClinicalTrials.gov ↗ · Chronic Rhinosinusitis with Nasal Polyps (CRSwNP), Biological Therapy, Biomarkers
Phase 4 Not yet open Beijing Tongren Hospital China
Study of Stapokibart Injection in Subjects With Moderate to Severe Bullous Pemphigoid
NCT07210554 · ClinicalTrials.gov ↗ · Bullous Pemphigoid (BP)
Phase 3 Not yet open Chengdu Kangnuoxing Biopharma,Inc China
Study of Stapokibart Injection in Adolescent Subjects With Seasonal Allergic Rhinitis (SAR)
NCT07617324 · ClinicalTrials.gov ↗ · Seasonal Allergic Rhinitis (SAR)
Phase 2 Not yet open Chengdu Kangnuoxing Biopharma,Inc China
A Prospective Study of Stapokibart Injection in Patients With Seasonal Allergic Rhinitis (SAR)
NCT07459556 · ClinicalTrials.gov ↗ · SAR
Observational Not yet open Chengdu Kangnuoxing Biopharma,Inc China
Efficacy and Safety of Stapokibart in Non-Allergic Rhinitis With Eosinophilia Syndrome
NCT07240376 · ClinicalTrials.gov ↗ · Non-Allergic Rhinitis With Eosinophilia Syndrome
Not applicable Not yet open Huazhong University of Science and Technology China
Preoperative Stapokibart for Endoscopic Sinus Surgery in Chronic Rhinosinusitis With Nasal Polyps
NCT07616609 · ClinicalTrials.gov ↗ · Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)
Not applicable Not yet open Beijing Tongren Hospital China
Study of CM310 in Adolescent Subjects With Atopic Dermatis
NCT06495229 · ClinicalTrials.gov ↗ · Atopic Dermatitis
Phase 3 Active, closed Keymed Biosciences Co.Ltd China
A Study of Stapokibart Injection in Patients With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)
NCT07483268 · ClinicalTrials.gov ↗ · CRSWNP
Observational Active, closed Chengdu Kangnuoxing Biopharma,Inc 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.

02

Conditions studied with Stapokibart

12 conditions
Seasonal Allergic Rhinitis (SAR)2Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)1CRSWNP1Atopic Dermatitis (AD)1Non-Allergic Rhinitis With Eosinophilia Syndrome1Bullous Pemphigoid (BP)1SAR1Chronic Rhinosinusitis with Nasal Polyps (CRSwNP)1Biological Therapy1Biomarkers1Moderate to Severe Asthma1Atopic Dermatitis1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Chengdu Kangnuoxing Biopharma,Inc6
Beijing Tongren Hospital2
Huazhong University of Science and Technology1
CSPC ZhongQi Pharmaceutical Technology Co., Ltd1
Keymed Biosciences Co.Ltd1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China113
Clinical trials in Japan22

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Stapokibart trials

How many clinical trials are testing Stapokibart?

11 current trials in our China and Japan registers name Stapokibart (also registered as CM310) as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Stapokibart trials recruiting patients?

Yes. 3 of the 11 trials are recruiting: 3 with sites in China and 2 with sites in Japan. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Stapokibart clinical trials?

Chengdu Kangnuoxing Biopharma,Inc (6), Beijing Tongren Hospital (2), Huazhong University of Science and Technology (1) and CSPC ZhongQi Pharmaceutical Technology Co., Ltd (1), among 5 lead sponsors in total. 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 Stapokibart works or whether it is effective, and it is not medical advice.

Approvals, shortages and trials, every Friday

One email a week with new EMA and FDA approvals, EU and US medicine shortages, how many trials are recruiting in Ireland, and the week's Irish pharma news.

Free. Unsubscribe from any email with one click. See our privacy policy.

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 Stapokibart works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Stapokibart (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 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.