Evidence map›Paper›PMID 28209624›Full record

Trial reportGut2017

Tofacitinib for induction and maintenance therapy of Crohn's disease: results of two phase IIb randomised placebo-controlled trials.

Julian Panés, William J Sandborn, Stefan Schreiber, Bruce E Sands, Séverine Vermeire, Geert D'Haens, Remo Panaccione, Peter D R Higgins, Jean-Frederic Colombel, Brian G Feagan and 7 more

3 registry-linked trialsAbstract readClinical Trial, Phase IIMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Gut, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 178 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
178citing papers in PubMed, 6 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.

NCT01393626 phase2completednot on this map

A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multi-Centre Study To Investigate The Safety And Efficacy Of CP-690,550 For Induction Therapy In Subjects With Moderate To Severe Crohn's Disease

TypeinterventionalSponsorPfizerRan2011 to 2015Enrolled280ConditionsCrohn's DiseaseArmsPlacebo, CP-690,550
NCT01393899 phase2completednot on this map

A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multi-Centre Study To Investigate The Safety And Efficacy Of CP-690,550 For Maintenance Therapy In Subjects With Moderate To Severe Crohn's Disease

TypeinterventionalSponsorPfizerRan2012 to 2015Enrolled180ConditionsCrohn's DiseaseArmsPlacebo, CP-690,550
NCT05104723 phase1 / phase2completednot on this mapstarted 2022, after this paper: background citation

A Phase 1/2 Open-label Study to Evaluate the Safety and Efficacy of Tofacitinib for Chronic Granulomatous Disease With Inflammatory Complications

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2022 to 2026Enrolled10ConditionsChronic Granulomatous Disease, Inflammatory Gastrointestinal Disease, Inflammatory Skin Disease, Inflammatory Lung DiseaseArmsXELJANZ (tofacitinib)
3 · Its place in the literature

Who cites it

178 citing papers in PubMed, 6 syntheses or guidelines pooled it.

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  18. Updated review of Janus kinase inhibitors for the management of inflammatory bowel disease.World journal of gastrointestinal pharmacology and therapeutics · 2026
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118 more citing papers are in PubMed but not listed here.

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

17 authors.

Julian PanésHospital Clinic de Barcelona, IDIBAPS, CIBERehd, Barcelona, Spain.
William J SandbornDivision of Gastroenterology, Department of Medicine, University of California, San Diego, La Jolla, California, USA.
Stefan SchreiberKlinik für Innere Medizin I, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Bruce E SandsDr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Séverine VermeireDepartment of Gastroenterology, University Hospitals Leuven, Leuven, Belgium.
Geert D'HaensAcademic Medical Centre, University of Amsterdam, Amsterdam, The Netherlands.
Remo PanaccioneDepartment of Medicine, University of Calgary, Calgary, Alberta, Canada.
Peter D R HigginsDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Jean-Frederic ColombelDr. Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Brian G FeaganRobarts Research Institute, London, Ontario, Canada.
Gary ChanPfizer Inc, Collegeville, Pennsylvania, USA.
Michele MoscarielloPfizer Inc, Collegeville, Pennsylvania, USA.
Wenjin WangPfizer Inc, Collegeville, Pennsylvania, USA.
Wojciech NiezychowskiPfizer Inc, Collegeville, Pennsylvania, USA.
Amy MarrenPfizer Inc, Collegeville, Pennsylvania, USA.
Paul HealeyPfizer Inc, Groton, Connecticut, USA.
Eric MallerPfizer Inc, Collegeville, Pennsylvania, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTofacitinib is an oral, small-molecule Janus kinase inhibitor that is being investigated for IBD. We evaluated the efficacy and safety of tofacitinib for induction and maintenance treatment in patients with moderate-to-severe Crohn's disease (CD).

designWe conducted two randomised, double-blind, placebo-controlled, multicentre phase IIb studies. Adult patients with moderate-to-severe CD were randomised to receive induction treatment with placebo, tofacitinib 5 or 10 mg twice daily for 8 weeks. Those achieving clinical response-100 or remission were re-randomised to maintenance treatment with placebo, tofacitinib 5 or 10 mg twice daily for 26 weeks. Primary endpoints were clinical remission at the end of the induction study, and clinical response-100 or remission at the end of the maintenance study.

results180/280 patients randomised in the induction study were enrolled in the maintenance study. At week 8 of induction, the proportion of patients with clinical remission was 43.5% and 43.0% with 5 and 10 mg twice daily, respectively, compared with 36.7% in the placebo group (p=0.325 and 0.392 for 5 and 10 mg twice daily vs placebo). At week 26 of maintenance, the proportion of patients with clinical response-100 or remission was 55.8% with tofacitinib 10 mg twice daily compared with 39.5% with tofacitinib 5 mg twice daily and 38.1% with placebo (p=0.130 for 10 mg twice daily vs placebo). Compared with placebo, the change in C-reactive protein from baseline was statistically significant (p<0.0001) with 10 mg twice daily after both induction and maintenance treatments.

conclusionsPrimary efficacy endpoints were not significantly different from placebo, although there was evidence of a minor treatment effect. No new safety signals were observed for tofacitinib. TRIAL REGISTRATION NUMBERS: NCT01393626 and NCT01393899.

Indexed as

AdultC-Reactive ProteinCrohn DiseaseDouble-Blind MethodFemaleHumansMaintenance ChemotherapyMaleMiddle AgedPiperidinesProtein Kinase InhibitorsPyrimidinesPyrrolesRemission InductionSeverity of Illness IndexC-Reactive ProteinPiperidinesProtein Kinase InhibitorsPyrimidinesPyrrolestofacitinibCLINICAL TRIALSCROHN'S DISEASEIMMUNOLOGY

Identifiers

PMID28209624
PMCPMC5532457

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

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.