Clinical trial No longer in our active list Phase 3 Interventional Ages 51 and up

Stopping Tocilizumab for Giant Cell Arteritis

Official title: TocilizuMab discontinuAtion in GIant Cell Arteritis

Run by Centre Hospitalier Universitaire Dijon · NCT06037460 · Data updated 2026-05-14

This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.

This study is testing what happens when people over 50 with Giant Cell Arteritis stop taking Tocilizumab to see if it affects their chances of having a relapse and helps manage their condition better.

More Giant Cell Arteritis trials

Quick facts

PhasePhase 3
Study typeInterventional
Ages51 Years and up
SexAll
Enrollment120 (estimated)
SponsorCentre Hospitalier Universitaire Dijon
Academic / other
Drugs / interventionstocilizumab, secukinumab, ustekinumab, Rituximab, Methotrexate, Cyclophosphamide, prednisone
Locations1 site (Dijon)
Trial IDNCT06037460 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals aged 50 and older diagnosed with Giant Cell Arteritis who meet specific clinical and laboratory criteria.

Probably not a fit

Patients with other underlying conditions that complicate GCA or those who do not meet the eligibility criteria may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the discontinuation of Tocilizumab, a medication used to treat Giant Cell Arteritis (GCA), in patients over 50 years old. The study aims to evaluate the effects of stopping this treatment on relapse rates and the overall management of GCA, which is often treated with corticosteroids. Participants will undergo assessments including questionnaires, blood samples, and 18FDG PET scans to monitor their condition and response to treatment. The goal is to find a safer and more effective approach to managing GCA while minimizing corticosteroid-related complications.

Why it matters

Potential benefit: If successful, this study could lead to improved management strategies for patients with Giant Cell Arteritis, reducing the need for long-term corticosteroid use.

How similar studies have gone: While there have been studies on GCA treatments, this specific approach to discontinuing Tocilizumab is novel and has not been extensively tested.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Written consent
* Diagnosis of GCA, defined by the following criteria:

  * Age ≥50 years at diagnosis
  * AND History of ESR ≥50 mm/h OR CRP ≥20 mg/L (optional criterion if temporal artery biopsy (TAB) is positive).
  * AND at least one of the following clinical criteria:

    * At least one unequivocal sign of GCA (recent headache, scalp hyperesthesia, jaw claudication, temporal artery abnormality, visual disturbances of ischemic origin)
    * Clinical sign(s) of polymyalgia rheumatica (PR)
  * AND at least one of the following criteria during GCA follow-up:

    * TAB consistent with the diagnosis of GCA (non-necrotizing vasculitis with a mononuclear cell-rich inflammatory infiltrate or presence of granulomas, with or without multinuclear giant cells)
    * Evidence of temporal artery vasculitis by echo-Doppler of the temporal arteries (unilateral or bilateral halo sign)
    * Evidence of vasculitis of at least one large vessel by imaging:
  * angio-CT or angio-MRI: arterial wall thickening (≥2mm for aorta; ≥1mm for supra-aortic trunks and upper extremity arteries, ≥0.6mm for the cephalic artery, ...) and/or T1-weighted contrast.
  * PET: grade 2 or 3\* hypermetabolism of the wall of at least one large vessel (aorta, supra-aortic trunks, cephalic vessels, upper extremity arteries) (\*i.e., arterial SUVmax ≥ liver SUVmax)
* GCA in remission for at least 12 weeks before randomisation (remission = absence of symptoms due to GCA AND CRP ≤10 mg/L)
* TCZ treatment (IV or SC) or biosimilar initiated 12 to 36 months prior to randomization
* TCZ treatment (IV or SC) or biosimilar not interrupted more than 12 weeks in the 12 months prior to randomization
* Treatment with subcutaneous TCZ (162 mg/week) or biosimilar for at least 12 consecutive weeks prior to randomization
* Treatment with corticoids stopped at least 12 weeks before randomization (hydrocortisone treatment ≤20 mg/day is possible if given at a stable dose for the duration of the study)
* Biological workup dating from less than 6 weeks on the day of randomization, showing good tolerance of tocilizumab:

  * AST and ALT \< 1.5 x upper limit of normal (ULN)
  * Hemoglobin \>8 g/dL
  * Platelets \>100 G/L
  * Neutrophils \>1 G/L
  * Lymphocytes \>0.5 G/L

Exclusion Criteria:

* Person who is not affiliated with the national health insurance system
* Person subject to a measure of legal protection (guardianship, tutorship)
* Person subject to a court order
* Patient unable to give consent
* Person who does not speak French
* Pre-menopausal women (menopause = amenorrhea of more than 12 consecutive months)
* Uncontrolled psychotic state
* History of drug or alcohol intoxication requiring hospitalization within 12 months prior to randomization
* Recent or scheduled surgery within 6 months of randomization
* History of organ or hematopoietic marrow transplantation (except corneal transplantation performed at least 12 weeks prior to randomization)
* Primary or secondary immune deficiency
* Concomitant treatment with any of the following:

  * Methotrexate, leflunomide, cyclosporin A, azathioprine, mycophenolate mofetil, Janus kinase inhibitors, abatacept, secukinumab, anti-TNF-α, anakinra, ustekinumab, or any other immunosuppressive drug within 12 weeks prior to randomization
  * Rituximab or other anti-CD20 agent within 1 year prior to randomization
  * Cyclophosphamide in the year prior to randomization
* History of long-term corticosteroid therapy for conditions other than GCA or PPR. (NB: dermocorticoids, inhaled corticosteroids, and corticosteroid joint infiltrations are allowed during the study)
* Patient who has previously received ≥3 courses of oral corticosteroids for a disease other than GCA or RRP within 6 months prior to randomization
* Ongoing anti-tuberculosis treatment at the time of randomization
* Infections:

  * Current viral hepatitis B or C
  * Ongoing HIV infection
  * Severe infection requiring hospitalization within 30 days prior to randomization
* Any unstable or poorly controlled condition or disease, acute or chronic, not related to GCA, and considered a contraindication to tocilizumab therapy in the opinion of the investigator
* Neoplasia \< 5 years, (except cervical cancer in situ and skin carcinoma, except melanoma, with R0 resection)

Where it's running

  • Chu Dijon Bourgogne
    Dijon, France
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.