Evidence map›Paper›PMID 41781163›Full record

Trial reportRMD open2026

Nipocalimab and certolizumab combination therapy in participants with active rheumatoid arthritis despite prior treatment with advanced therapies: results from the phase 2a DAISY-RA study.

Peter C Taylor, Georg Schett, Tom W J Huizinga, Fowzia Ibrahim, Bei Zhou, Sicong Huang, Jay Gambale, Qingmin Wang, Sophia G Liva, Jocelyn H Leu and 5 more

Abstract readClinical Trial, Phase IIRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in RMD open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Peter C TaylorNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK peter.taylor@kennedy.ox.ac.uk.ORCID 0000-0001-7766-6167
Georg SchettDepartment of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) and Universitätsklinikum Erlangen, Erlangen, Germany.
Tom W J HuizingaLeiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-7033-7520
Fowzia IbrahimJohnson & Johnson, Wycombe, UK.
Bei ZhouJohnson & Johnson, Chesterbrook, Pennsylvania, USA.
Sicong HuangJohnson & Johnson, Cambridge, Massachusetts, USA.
Jay GambaleJohnson & Johnson, Spring House, Pennsylvania, USA.
Qingmin WangJohnson & Johnson, Spring House, Pennsylvania, USA.
Sophia G LivaJohnson & Johnson, Spring House, Pennsylvania, USA.
Jocelyn H LeuJohnson & Johnson, Spring House, Pennsylvania, USA.
Jonathan J HubbardJohnson & Johnson, Spring House, Pennsylvania, USA.
Steven LeonardoJohnson & Johnson, Spring House, Pennsylvania, USA.
Rohit A PanchakshariJohnson & Johnson, La Jolla, California, USA.
Matthew J LozaJohnson & Johnson, Spring House, Pennsylvania, USA.
Kaiyin FeiJohnson & Johnson, Spring House, Pennsylvania, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo investigate the efficacy, safety, pharmacokinetics, immunogenicity and pharmacodynamics of combination therapy with nipocalimab and certolizumab in participants with active rheumatoid arthritis (RA) despite treatment with advanced therapies.

methodsIn this phase 2a study, participants were randomised 3:2 to receive combination therapy with nipocalimab (intravenous 30 mg/kg) and certolizumab (subcutaneous 400 mg at weeks 0, 2, 4, then 200 mg) or certolizumab monotherapy every 2 weeks from weeks 0 to 24. The primary endpoint was change from baseline in Disease Activity Score 28 using C-reactive protein (DAS28-CRP) at week 12. Other outcomes were assessed through week 30.

results103 participants were enrolled (combination therapy/monotherapy, n=62/41). At week 12, the primary endpoint was similar between groups (least squares mean 90% CI -1.92 (-2.48 to -1.36) vs -1.86 (-2.44 to -1.28); p=0.822). Secondary endpoints were also similar between groups, although numerically higher proportions of participants treated with combination therapy versus monotherapy achieved ≥50% response in American College of Rheumatology criteria (ACR50), DAS28-CRP <2.6 and DAS28-CRP ≤3.2 at week 12. Serious adverse events were reported in 11.3% of participants in the combination therapy group and 2.4% in the monotherapy group. In combination with certolizumab, nipocalimab exhibited nonlinear pharmacokinetics with accelerated clearance and substantially, reversibly reduced serum immunoglobulin G, including anticitrullinated protein antibody levels.

conclusionsCombination therapy of nipocalimab with certolizumab showed a similar outcome in the primary endpoint and secondary endpoints compared with certolizumab monotherapy in participants with active RA.

Indexed as

Antibodies, Monoclonal, HumanizedAntirheumatic AgentsArthritis, RheumatoidCertolizumab PegolAdultAgedCombined Antibody TherapeuticsDrug Therapy, CombinationFemaleHumansMaleMiddle AgedTreatment OutcomeAntibodies, Monoclonal, HumanizedAntirheumatic AgentsCertolizumab PegolCombined Antibody TherapeuticsnipocalimabAntibodiesAnti-Citrullinated Protein AntibodiesArthritis, RheumatoidTumor Necrosis Factor Inhibitors

Identifiers

PMID41781163
PMCPMC13266242

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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.