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1000 Titel
  • The Meteoritics Trial: efficacy of methotrexate after remission-induction with tocilizumab and glucocorticoids in giant cell arteritis—study protocol for a randomized, double-blind, placebo-controlled, parallel-group phase II study
1000 Autor/in
  1. Kreis, Lena |
  2. Dejaco, Christian |
  3. Schmidt, Wolfgang Andreas |
  4. Németh, Robert |
  5. Venhoff, Nils |
  6. Schäfer, Valentin Sebastian |
1000 Verlag BioMed Central
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-01-15
1000 Erschienen in
1000 Quellenangabe
  • 25(1):56
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13063-024-07905-4 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10790384/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>Glucocorticoids (GC) are the standard treatment for giant cell arteritis (GCA), even though they are associated with adverse side effects and high relapse rates. Tocilizumab (TCZ), an interleukin-6 receptor antagonist, has shown promise in sustaining remission and reducing the cumulative GC dosage, but it increases the risk of infections and is expensive. After discontinuation of TCZ, only about half of patients remain in remission. Additionally, only few studies have been conducted looking at remission maintenance, highlighting the need for alternative strategies to maintain remission in GCA. Methotrexate (MTX) has been shown to significantly decrease the risk of relapse in new-onset GCA and is already a proven safe drug in many rheumatologic diseases.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>This study aims to evaluate the efficacy and safety of MTX in maintaining remission in patients with GCA who have previously been treated with GC and at least 6 months with TCZ. We hypothesize that MTX can maintain remission in GCA patients, who have achieved stable remission after treatment with GC and TCZ, and prevent the occurrence of relapses. The study design is a monocentric, randomized, double-blind, placebo-controlled, parallel-group phase II trial randomizing 40 GCA patients 1:1 into a MTX or placebo arm. Patients will receive 17.5 mg MTX/matching placebo weekly by subcutaneous injection for 12 months, with the possibility of dose reduction if clinically needed. A 6-month follow-up will take place. The primary endpoint is the time to first relapse in the MTX group versus placebo during the 12-month treatment period. Secondary outcomes include patient- and investigator-reported outcomes and laboratory findings, as well as the prevalence of aortitis, number of vasculitic vessels, and change in intima-media thickness during the study.</jats:p> </jats:sec><jats:sec> <jats:title>Discussion</jats:title> <jats:p>This is the first clinical trial evaluating remission maintenance of GCA with MTX after a previous treatment cycle with TCZ. Following the discontinuation of TCZ in GCA, MTX could be a safe and inexpensive drug.</jats:p> </jats:sec><jats:sec> <jats:title>Trial registration</jats:title> <jats:p>ClinicalTrials.gov, NCT05623592. Registered on 21 November 2022.</jats:p> <jats:p>EU Clinical Trials Register, 2022-501058-12-00.</jats:p> <jats:p>German Clinical Trials Register DRKS00030571.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Methotrexate
lokal Giant cell arteritis
lokal Double-Blind Method [MeSH]
lokal Remission maintenance
lokal Rheumatic disease
lokal Methotrexate [MeSH]
lokal Carotid Intima-Media Thickness [MeSH]
lokal Study Protocol
lokal Vasculitis
lokal Humans [MeSH]
lokal Treatment Outcome [MeSH]
lokal Glucocorticoids [MeSH]
lokal Giant Cell Arteritis/diagnosis [MeSH]
lokal Recurrence [MeSH]
lokal Ultrasound
lokal Phase II trial
lokal Randomized Controlled Trials as Topic [MeSH]
lokal Tocilizumab
lokal Glucocorticoids
lokal Antibodies, Monoclonal, Humanized [MeSH]
lokal Neoplasm Recurrence, Local [MeSH]
lokal Giant Cell Arteritis/drug therapy [MeSH]
lokal Clinical Trials, Phase II as Topic [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/S3JlaXMsIExlbmE=|https://frl.publisso.de/adhoc/uri/RGVqYWNvLCBDaHJpc3RpYW4=|https://frl.publisso.de/adhoc/uri/U2NobWlkdCwgV29sZmdhbmcgQW5kcmVhcw==|https://frl.publisso.de/adhoc/uri/TsOpbWV0aCwgUm9iZXJ0|https://frl.publisso.de/adhoc/uri/VmVuaG9mZiwgTmlscw==|https://orcid.org/0000-0002-6591-5936
1000 Hinweis
  • DeepGreen-ID: 4ac4f142f8644f9c9bc6a1c580b7c5c7 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. Medizinische Fakultät, Rheinische Friedrich-Wilhelms-Universität Bonn |
  2. Medac |
  3. Universitätsklinikum Bonn |
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1000 Förderprogramm
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1000 Dateien
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    1000 Förderer Medizinische Fakultät, Rheinische Friedrich-Wilhelms-Universität Bonn |
    1000 Förderprogramm -
    1000 Fördernummer -
  2. 1000 joinedFunding-child
    1000 Förderer Medac |
    1000 Förderprogramm -
    1000 Fördernummer -
  3. 1000 joinedFunding-child
    1000 Förderer Universitätsklinikum Bonn |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 Erstellt am 2025-07-05T15:08:43.362+0200
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1000 Zuletzt bearbeitet 2025-08-14T08:07:33.175+0200
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