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New hope for rare joint disease: arthritis drug tocilizumab tested in CPPD

NCT ID NCT07254637

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether tocilizumab, an anti-inflammatory drug already used for rheumatoid arthritis, can reduce joint pain and improve quality of life in people with chronic inflammatory calcium pyrophosphate deposition disease (CPPD) that hasn't improved with standard treatments. Eighty adults will receive monthly infusions of tocilizumab or a placebo for three months. The main goal is to see if pain decreases after treatment.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
tocilizumab (a drug that blocks inflammation, given as an IV infusion)
What this could lead to
If it works, this could offer a new treatment option for people with chronic inflammatory CPPD who have not responded to standard therapies.
What could go wrong
This is a small, early-phase trial (Phase 2) with only 80 participants. The drug may not prove effective, and side effects from tocilizumab (such as infections) are possible.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

About 80 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Apr 2026

An estimate. Start dates often move.

Expected to finish

Nov 2029

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Adults \> 18 years * Diagnosis of CPPD according to ACR/EULAR 2023 classification criteria * Persistent inflammatory pain (\> 3 months) or ≥ 2 arthritics/month * Number of painful joints (NAD) \> 3 * Overall pain VAS (0\_100) \> 40 mm * Failure, intolerance or impossibility of repeated use of usual treatments: colchicine, NSAIDs, corticosteroids and anakinra * Use of an effective method of contraception in women of childbearing age until 3 months after the end of the study. * Informed consent Exclusion Criteria: * Presence of anti-CPP antibodies \> 50 IU/ml * Recurrent or chronic infections * History of severe infection (= requiring hospitalization) * Active infection * Vaccination with live or attenuated vaccine within 4 weeks prior to inclusion * History of intestinal ulceration or diverticulitis Untreated latent tuberculosis * History of viral hepatitis B ou C * Symptoms suggestive of demyelinating disease of the central nervous system * History of cancer, active cancer, or suspected cancer * Neutropenia \< 2000 elements/mm3, thrombocytopenia \< 100 000/mm3 * Elevated transaminases \> 3 x ULN * Known hypersensitivity to the active substance or one of the excipients; * Known severe immune deficiency * Patients not meeting classification criteria * Concomitant treatment with biological or targeted therapies, or immunosuppressive therapy (including methotrexate, leflunomide, azathioprine), systemic corticosteroids, anakinra, IL-6 inhibitors in subcutaneous injection, anti-TNF agents, and JAK. If these treatments are used before inclusion, a washout period corresponding to at least five times their respective mean terminal half-life must be respected. * inhibitors. * Previous treatment with tocilizumab * Concomitant treatment with methylprednisolone, dexamethasone, atorvastatin, calcium channel blockers, theophylline, warfarin, phenprocoumon, phenytoin, cyclosporine or benzodiazepines * Dyslipidemia, hypertension or poorly controlled cardiovascular disease * Scheduled surgery * Difficulty to understand French, illiteracy * Pregnant women, women in labor or nursing mothers * Persons deprived of their liberty, adults under legal protection or unable to express their consent * Persons not affiliated to a social security scheme or beneficiaries of such a scheme * Participation in another interventional study

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    12 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • CHU de Dijon

    Dijon, 21000, France

  • CHU de Nantes

    Nantes, 44000, France

  • CHU de Rennes

    Rennes, 35200, France

  • CHU de Saint-Étienne

    Saint-Etienne, 42100, France

  • Centre Hospitalier Sud-Francilien

    Corbeil-Essonnes, Paris, 91100, France

  • Groupe Hospitalier Intercommunal Le Raincy-Montfermeil

    Paris, 93370, France

  • Groupe Hospitalier de l'Institut Catholique de Lille

    Lomme, Lille, 59462, France

  • Hôpital Bichat Claude-Bernard

    Paris, 75018, France

  • Hôpital Le Kremlin Bicêtre

    Paris, 94270, France

  • Hôpital Tenon

    Paris, 75020, France

  • Hôpital de la Croix Saint-Simon

    Paris, 75020, France

  • Lariboisière hospital

    Paris, Paris Paris, 75010, France