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Priya Life Science Compound trial record
Compound · clinical trials

Firsekibart clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 5 trials in our China register that name Firsekibart as an intervention. Synced 10 Nov 2026
5Current trials
0Recruiting now
5Lead sponsors
1Country register
At a glance

Firsekibart is named as an intervention in 5 current clinical trials in our China register. None are recruiting at the moment. The most common phase is Not applicable. The sponsor with the most trials is Second Affiliated Hospital, Zhejiang University, School of Medicine (1). The most-studied condition is Gout Flare.

Patient leaflets for Firsekibart

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

  • Not yet open360%
  • Active, closed240%

Trials by phase

  • Not applicable240%
  • Phase 4120%
  • Observational120%
  • Phase 2/3120%
01

Clinical trials of Firsekibart

5 trials
StudyPhaseStatusLead sponsorRegisters
Efficacy and Safety of Immunoglobulin Plus Firsekibart in Patients With Kawasaki Disease
NCT07686770 · ClinicalTrials.gov ↗ · Kawasaki Disease
Phase 2/3 Not yet open Children's Hospital of Fudan University China
Efficacy and Safety of Firsekibart in the Treatment of Systemic Sclerosis
NCT07502105 · ClinicalTrials.gov ↗ · Systemic Scleroderma
Not applicable Not yet open Tongji Hospital China
24-Week Recurrence Rate of Gout Following Firsekibart Treatment
NCT07625514 · ClinicalTrials.gov ↗ · Gout Flare
Not applicable Not yet open Second Affiliated Hospital, Zhejiang University, School of Medicine China
Efficacy and Safety of IL-1 Inhibitors in Mild to Moderate Systemic Lupus Erythematosus
NCT07381465 · ClinicalTrials.gov ↗ · Lupus Erythematosus, Systemic
Phase 4 Active, closed Chinese SLE Treatment And Research Group China
A Study of Firsekibart Versus Anakinra in Adult-Onset Still's Disease
NCT07191444 · ClinicalTrials.gov ↗ · Still's Disease, Adult-Onset
Observational Active, closed Ruijin Hospital 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 Firsekibart

5 conditions
Gout Flare1Lupus Erythematosus, Systemic1Still's Disease, Adult-Onset1Kawasaki Disease1Systemic Scleroderma1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Second Affiliated Hospital, Zhejiang University, School of Medicine1
Chinese SLE Treatment And Research Group1
Ruijin Hospital1
Children's Hospital of Fudan University1
Tongji Hospital1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China50

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

05

Related compounds

06

Questions about Firsekibart trials

How many clinical trials are testing Firsekibart?

5 current trials in our China register name Firsekibart as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Firsekibart trials recruiting patients?

Not at the moment. None of the 5 trials in our registers is recruiting; they are active but closed to enrolment, not yet open, or enrolling by invitation. Only the study team can confirm whether a patient is eligible.

Who sponsors Firsekibart clinical trials?

Second Affiliated Hospital, Zhejiang University, School of Medicine (1), Chinese SLE Treatment And Research Group (1), Ruijin Hospital (1) and Children's Hospital of Fudan University (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 Firsekibart works or whether it is effective, and it is not medical advice.

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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 Firsekibart 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 Firsekibart (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.