Evidence map›Paper›PMID 27440869›Full record

Trial reportJournal of Crohn's & colitis2017

Pharmacokinetics and Exposure-response Relationship of Golimumab in Patients with Moderately-to-Severely Active Ulcerative Colitis: Results from Phase 2/3 PURSUIT Induction and Maintenance Studies.

Omoniyi J Adedokun, Zhenhua Xu, Colleen W Marano, Richard Strauss, Hongyan Zhang, Jewel Johanns, Honghui Zhou, Hugh M Davis, Walter Reinisch, Brian G Feagan and 2 more

2 registry-linked trialsOpen access · hybridAbstract readClinical Trial, Phase IIClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in Journal of Crohn's & colitis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 51 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 4 pooled it
18.0field-weighted citation impact, top 1% of its field
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.

NCT03669029 phase4unknown statusnot on this mapstarted 2018, after this paper: background citation

Optimization of Golimumab Treatment in Ulcerative Colitis

TypeinterventionalSponsorHospital de ManisesRan2018 to 2019Enrolled50ConditionsColitis, UlcerativeArmsGolimumab 50 mg in patients <80 kg and Golimumab 100 mg in patients >80 kg, Golimumab treatment optimization.
NCT03773445 completednot on this mapstarted 2019, after this paper: background citation

Association of Golimumab Trough Levels With Endoscopic and Histologic Healing in Patients With Ulcerative Colitis

TypeobservationalSponsorHospital San Carlos, MadridRan2019 to 2021Enrolled52ConditionsUlcerative ColitisArmsGolimumab trough levels, Antibodies to golimumab, Histology, Colonoscopy
3 · Its place in the literature

Who cites it

51 citing papers in PubMed, 4 syntheses or guidelines pooled it, 114 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Pooled it
  4. Anti-Drug Antibody Formation Against Biologic Agents in Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2021
    Pooled it
  5. Trial
  6. Trial
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Observational
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Review
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

12 authors at 5 institutions in 3 countries.

Omoniyi J AdedokunDepartment of Global Clinical Pharmacology, Janssen Research & Development, LLC, Spring House, PA, USA OAdedoku@its.jnj.com.
Zhenhua XuDepartment of Global Clinical Pharmacology, Janssen Research & Development, LLC, Spring House, PA, USA.
Colleen W MaranoDepartment of Clinical Development Immunology, Janssen Research & Development, LLC, Spring House, PA, USA.
Richard StraussDepartment of Translational Medicine Sciences, Janssen Research & Development, LLC, Spring House, PA, USA.
Hongyan ZhangDepartment of Global Clinical Pharmacology, Janssen Research & Development, LLC, Spring House, PA, USA.
Jewel JohannsDepartment of Clinical Biostatistics, Janssen Research & Development, LLC, Spring House, PA, USA.
Honghui ZhouDepartment of Global Clinical Pharmacology, Janssen Research & Development, LLC, Spring House, PA, USA.
Hugh M DavisDepartment of Biologics Development Sciences, Janssen Research & Development, LLC, Spring House, PA, USA.
Walter ReinischDepartment of Gastroenterology, Universitätsklinik für Innere Medizin III, Vienna, Austria & McMaster University, Hamilton, ON, Canada.
Brian G FeaganDepartment of Gastroenterology, Robarts Research Institute, University of Western Ontario, London, ON, Canada.
Paul RutgeertsDepartment of Gastroenterology, Hospital Gasthuisberg, Leuven, Belgium.
William J SandbornDepartment of Gastroenterology, University of California San Diego, La Jolla, CA, USA.
Janssen (United States) · USMcMaster University · CAUniversitair Ziekenhuis Leuven · BEUniversity of California, San Diego · USWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsTo assess golimumab pharmacokinetics [PK] and exposure-response [ER] in adults with moderate-to-severe ulcerative colitis [UC] from the Program of Ulcerative Colitis Research Studies Utilizing an Investigational Treatment [PURSUIT] studies.

methodsWe analysed golimumab PK and ER data of patients with moderate-to-severe UC from the PURSUIT-subcutaneous induction [N = 1064] and maintenance [N = 464] studies. Induction analyses evaluated serum golimumab concentration [SGC] and efficacy data through Week [wk] 6 following subcutaneous doses at wk0 and wk2; maintenance analyses assessed data through wk54 following 4-weekly dosing. ER relationships were assessed using trend, logistic regression, and receiver-operating-characteristic curve analyses.

resultsMedian SGCs peaked at induction wk2 for golimumab 100/50mg, 200/100mg, and 400/200mg. Wk6 median SGCs were 0.78, 1.78, and 4.01 μg/ml, respectively. SGCs were sustained, reaching steady state approximately 8wks after golimumab maintenance commenced [wk14 of golimumab] regardless of induction dose. Median trough SGCs from maintenance wks8-44 ranged from 0.69 to 0.83 µg/ml [50 mg] and 1.33-1.58 µg/ml [100 mg]. SGCs were approximately dose proportional, and higher SGCs were associated with higher efficacy response rates during induction and maintenance. Factors associated with golimumab exposure were body weight, antibody-to-golimumab status, serum albumin, alkaline phosphatase, faecal markers, C-reactive protein, and pancolitis. SGCs of 2.5 µg/ml [induction wk6] and 1.4 µg/ml [maintenance steady-state trough] are potential target concentrations. Immunomodulators had no apparent impact on SGC with golimumab 100mg, whereas drug levels were slightly higher with golimumab 50mg with vs without immunomodulators.

conclusionsSGCs are approximately dose proportional, and a positive SGC-efficacy relationship exists during induction/maintenance golimumab treatment of adult UC patients. Optimal SGC targets require validation in prospective studies.

Indexed as

AdolescentAdultAgedAntibodies, MonoclonalColitis, UlcerativeFemaleHumansMaleMiddle AgedRemission InductionSeverity of Illness IndexTreatment OutcomeTumor Necrosis Factor-alphaYoung AdultAntibodies, MonoclonalgolimumabTumor Necrosis Factor-alphaanti-tumour necrosis factorpharmacokineticsUlcerative colitis

Identifiers

PMID27440869
PMCPMC5175493
OpenAlexW2506322793

What OpenQuestion holds

Textmetadata
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.