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Still's Disease, Including SJIA and AOSD, With MAS or ILD ComplicationsNCT07889310

Managed Access Programs for MAS825, Arumakimig

A study testing Arumakimig in people with Still's Disease, Including SJIA and AOSD, With MAS or ILD Complications, run by Novartis Pharmaceuticals.

Temporarily Not Available

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The purpose of this registration is to list Managed Access Programs (MAPs) related to MAS825, arumakimig Read more about this study

Who is it for?
Ages 1 year and older
What is being tested?
Arumakimig
How many people
Not given
Where
No sites listed yet
Study dates
Start not givento not given
Phase
Expanded access
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 1 year and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • An independent request was received from a licensed physician. The patient has a serious or life-threatening disease or condition and there is no comparable or satisfactory alternative therapy available for diagnosis, monitoring, or treatment.
  • The patient is not eligible or able to enrol in a clinical trial or continue participation in such trial.
  • There is a potential patient benefit to justify the potential risk of the treatment use, and the potential risk is not unreasonable in the context of the disease or condition to be treated.
  • The patient must meet any other medical criteria established by the medical experts responsible for the product or by the health authority in the country of request (as applicable).
  • Provision of the product will not interfere with the initiation, conduct, or completion of a Novartis clinical trial or overall development program.
  • Managed Access provision is allowed per local laws/regulations.

Who cannot join

None listed.

About this study

The purpose of this registration is to list Managed Access Programs (MAPs) related to MAS825, arumakimig

Read the detailed description

CMAS825J12003M - Not yet available - Managed Access Program (MAP) to provide access to MAS825 to patients with Still's disease, including SJIA and AOSD, with MAS or ILD complications

Being tested
Arumakimig
Keywords
MAS825, Managed Access Program, MAP
Medical subject headings
Arthritis, Juvenile

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ArumakimigDrug

    Also called MAS825

    Patients receive arumakimig

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Oct 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Expanded access
IDs, dates and publications
ClinicalTrials.gov ID
NCT07889310
Sponsor's protocol ID
CMAS825J12003M
Status last verified
Oct 2026
First submitted
13 Oct 2026
Last updated
22 Oct 2026
Results posted
No

Questions about this trial

What is this clinical trial studying?

A study testing Arumakimig in people with Still's Disease, Including SJIA and AOSD, With MAS or ILD Complications, run by Novartis Pharmaceuticals.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 22 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Oct 2026.

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