Evidence map›Paper›PMID 38955475›Full record

Trial reportAnnals of the rheumatic diseases2024

Olokizumab plus methotrexate: safety and efficacy over 106 weeks of treatment.

Eugen Feist, Roy M Fleischmann, Saeed Fatenejad, Daria Bukhanova, Sergey Grishin, Sofia Kuzkina, Michael Luggen, Evgeniy Nasonov, Mikhail Samsonov, Josef S Smolen

Erratum issuedAbstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in Annals of the rheumatic diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Article
  7. The role of IL-6 in atherosclerosis: a narrative review.Frontiers in cardiovascular medicine · 2026
    Review
  8. Article
  9. Review
  10. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Eugen FeistRheumatology and Clinical Immunology, HELIOS Fachklinik Vogelsang/Gommern, Vogelsang, Germany Eugen.Feist@helios-gesundheit.de.ORCID http://orcid.org/0000-0002-9872-5282
Roy M FleischmannMedicine, University of Texas Southwestern, Dallas, Texas, USA.ORCID http://orcid.org/0000-0002-6630-1477
Saeed FatenejadSFC Medica, LLC, Charlotte, North Carolina, USA.ORCID http://orcid.org/0000-0002-3005-9439
Daria BukhanovaMedical, R-Pharm JSC, Moscow, Russian Federation.
Sergey GrishinMedical, R-Pharm JSC, Moscow, Russian Federation.
Sofia KuzkinaMedical, R-Pharm JSC, Moscow, Russian Federation.ORCID http://orcid.org/0000-0002-2230-5847
Michael LuggenUniversity of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
Evgeniy NasonovInstitute of Rheumatology, V.A. Nasonova Research, Moscow, Russian Federation.ORCID http://orcid.org/0000-0002-1598-8360
Mikhail SamsonovMedical, R-Pharm JSC, Moscow, Russian Federation.
Josef S SmolenDivision of Rheumatology, Department of Medicine 3, Medical University of Vienna, Wien, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo report long-term safety and tolerability of olokizumab (OKZ) in combination with methotrexate (MTX) in subjects with active rheumatoid arthritis (RA), using pooled data from three randomised clinical trials (RCT) followed by open-label extension (OLE) study.

methodsCumulative data from three phase 3 core trials and their OLE were analysed. Safety variables assessed included treatment-emergent adverse events (AEs), serious AEs (SAEs), AEs of special interest and laboratory results. Efficacy assessments included ACR20/50/70 responses, Disease Activity Score 28 (C-reactive protein) <3.2, CDAI remission and low disease activity (LDA), SDAI remission and LDA, HAQ-DI decrease of 0.22 unit and Boolean 2.0 remission.

resultsA total of 2304 patients received OKZ in combination with MTX either once every 2 weeks or once every 4 weeks. Event rates per 100 patient-years in OKZ every 2 weeks and OKZ every 4 weeks, respectively, were 9.57 and 9.13 for SAEs; 2.95 and 2.34 for serious infections; 0.09 and 0.05 for gastrointestinal perforations; 0.58 and 0.83 for major adverse cardiovascular events; and 0.45 and 0.50 for malignancies. No increase in the rate of any AE was observed over 106 weeks of treatment. The evaluation of laboratory variables demonstrated the expected changes, like neutropenia, elevation of liver enzymes and blood lipids. Clinical response rates remained stable during the OLE.

conclusionThe long-term safety and tolerability of OKZ in combination with MTX remained stable. The efficacy of OKZ was maintained through week 106. These findings support OKZ as a treatment option for patients with active RA.

Indexed as

Antibodies, Monoclonal, HumanizedAntirheumatic AgentsArthritis, RheumatoidDrug Therapy, CombinationMethotrexateAdultAgedFemaleHumansMaleMiddle AgedTreatment OutcomeAntibodies, Monoclonal, HumanizedAntirheumatic AgentsMethotrexateAntirheumatic AgentsArthritis, RheumatoidCytokines

Identifiers

PMID38955475
PMCPMC11503126

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.