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Compound · clinical trials

Arumakimig clinical trials

Also listed in trial records as MAS825
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 4 trials in our USA, France, Spain, Italy, Czechia, Japan, Germany, Netherlands, UK, Turkey, Canada, Belgium, Denmark and Austria registers that name Arumakimig as an intervention. Synced 1 Oct 2026
4Current trials
2Recruiting now
1Lead sponsor
14Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Arumakimig is named as an intervention in 4 current clinical trials in our USA, France, Spain, Italy, Czechia, Japan, Germany, Netherlands, UK, Turkey, Canada, Belgium, Denmark and Austria registers. 2 are recruiting patients now. All registered phases are Phase 2. The lead sponsor is Novartis Pharmaceuticals. The most-studied condition is NLRC4-GOF, AIFEC (Autoinflammation With Infantile Enterocolitis), XIAP Deficiency, CDC42 Mutations.

Trials by status

  • Recruiting250%
  • Active, closed250%

Trials by phase

  • Phase 24100%
01

Clinical trials of Arumakimig

4 trials
StudyPhaseStatusLead sponsorRegisters
A Phase II Trial to Evaluate the Clinical Efficacy, Safety and Tolerability of MAS825 in Pediatric and Adult Participants With Still's Disease
NCT07203001 · Stillยดs Disease
Phase 2 Recruiting Novartis Pharmaceuticals USA, Germany, France, Spain, Italy, Netherlands, Turkey, Canada
A 52-Week Study Evaluating the Efficacy and Safety of Arumakimig (MAS825) in Participants With VEXAS Followed by Open-Label Extension (OLE) Period
NCT07748624 · ClinicalTrials.gov ↗ · VEXAS Syndrome
Phase 2 Recruiting Novartis Pharmaceuticals Japan
Study of Efficacy and Safety of Investigational Treatments in Patients With Moderate to Severe Hidradenitis Suppurativa
NCT03827798 · ClinicalTrials.gov ↗ · Hidradenitis Suppurativa
Phase 2 Active, closed Novartis Pharmaceuticals USA, Germany, France, Spain, Netherlands, Belgium, Denmark, Austria, Czechia
Study to Evaluate the Efficacy, Safety and Tolerability of MAS825 in Patients With Monogenic IL-18 Driven Autoinflammatory Diseases, Including NLRC4-GOF, XIAP Deficiency, or CDC42 Mutations
NCT04641442 · NLRC4-GOF, AIFEC (Autoinflammation With Infantile Enterocolitis), XIAP Deficiency, CDC42 Mutations
Phase 2 Active, closed Novartis Pharmaceuticals UK, USA, France, Spain, Italy, Czechia, Japan

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 Arumakimig

4 conditions
NLRC4-GOF, AIFEC (Autoinflammation With Infantile Enterocolitis), XIAP Deficiency, CDC42 Mutations1Stillยดs Disease1Hidradenitis Suppurativa1VEXAS Syndrome1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Novartis Pharmaceuticals4
04

By country register

RegisterTrialsRecruiting
Clinical trials in USA31
Clinical trials in France31
Clinical trials in Spain31
Clinical trials in Italy21
Clinical trials in Czechia20
Clinical trials in Japan21
Clinical trials in Germany21
Clinical trials in Netherlands21
Clinical trials in UK10
Clinical trials in Turkey11
Clinical trials in Canada11
Clinical trials in Belgium10
Clinical trials in Denmark10
Clinical trials in Austria10

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

05

Related compounds

06

Questions about Arumakimig trials

How many clinical trials are testing Arumakimig?

4 current trials in our USA, France, Spain, Italy, Czechia, Japan, Germany, Netherlands, UK, Turkey, Canada, Belgium, Denmark and Austria registers name Arumakimig (also registered as MAS825) as a drug or biological intervention, as of the registry sync on 1 October 2026. Completed and withdrawn studies are not counted.

Are Arumakimig trials recruiting patients?

Yes. 2 of the 4 trials are recruiting: 1 with sites in USA, 1 with sites in France, 1 with sites in Spain, 1 with sites in Italy, 1 with sites in Japan, 1 with sites in Germany, 1 with sites in Netherlands, 1 with sites in Turkey and 1 with sites in Canada. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Arumakimig clinical trials?

The lead sponsor is Novartis Pharmaceuticals. 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 Arumakimig 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 โ€” it is not written from memory, and nothing here describes how Arumakimig 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 Arumakimig (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 1 Oct 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 โ€” 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 โ€” we correct promptly and log it.