New hope for rare joint disease: arthritis drug tocilizumab tested in CPPD
NCT ID NCT07254637
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
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Apr 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2029
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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.
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The places running it
12 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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CHU de Dijon
Dijon, 21000, France
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CHU de Nantes
Nantes, 44000, France
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CHU de Rennes
Rennes, 35200, France
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CHU de Saint-Étienne
Saint-Etienne, 42100, France
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Centre Hospitalier Sud-Francilien
Corbeil-Essonnes, Paris, 91100, France
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Groupe Hospitalier Intercommunal Le Raincy-Montfermeil
Paris, 93370, France
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Groupe Hospitalier de l'Institut Catholique de Lille
Lomme, Lille, 59462, France
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Hôpital Bichat Claude-Bernard
Paris, 75018, France
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Hôpital Le Kremlin Bicêtre
Paris, 94270, France
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Hôpital Tenon
Paris, 75020, France
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Hôpital de la Croix Saint-Simon
Paris, 75020, France
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Lariboisière hospital
Paris, Paris Paris, 75010, France