Evidence map›Paper›PMID 14722206›Full record

Trial reportAnnals of the rheumatic diseases2004

Inhibition of leukotriene B4-induced CD11B/CD18 (Mac-1) expression by BIIL 284, a new long acting LTB4 receptor antagonist, in patients with rheumatoid arthritis.

R Alten, E Gromnica-Ihle, C Pohl, J Emmerich, J Steffgen, R Roscher, R Sigmund, B Schmolke, G Steinmann

Open access · bronzeAbstract readClinical TrialRandomized Controlled Trial
In one paragraph

Trial report in Annals of the rheumatic diseases, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.4field-weighted citation impact, top 8% 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.

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

14 citing papers in PubMed, 50 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. A LTBiScience · 2024
    Article
  5. Activation of leukotriene BCellular & molecular immunology · 2024
    Article
  6. Review
  7. Rheumatoid arthritis mediator CD18 expression byIranian journal of microbiology · 2019
    Article
  8. Systemic leukotriene BThe Journal of physiology · 2016
    Article
  9. Hyaluronidase decreases neutrophils infiltration to the inflammatory site.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2016
    Article
  10. BIIL 284 reduces neutrophil numbers but increases P. aeruginosa bacteremia and inflammation in mouse lungs.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2014
    Article
  11. Myeloid-related protein activity in rheumatoid arthritis.International journal of inflammation · 2011
    Article
  12. Article
  13. Article
  14. 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

9 authors at 5 institutions in 2 countries.

R AltenRheumatologie und Physikalische Therapie, Schlossparkklinik, Heubnerweg 2, D-14059 Berlin, FRG.
E Gromnica-Ihle
C Pohl
J Emmerich
J Steffgen
R Roscher
R Sigmund
B Schmolke
G Steinmann
Boehringer Ingelheim (Germany) · DEHelios Hospital Berlin-Buch · DESchlosspark-Klinik · DEPraxis · EEUniversity of Applied Sciences Biberach · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLeukotriene B4 (LTB(4)) has a key role in the pathophysiology of rheumatoid arthritis (RA).

objectiveTo investigate the inhibition of ex vivo LTB(4)-induced Mac-1 (CD11b/CD18) expression in leucocytes of patients with RA by the new oral LTB(4) receptor antagonist BIIL 284.

methodsThe pharmacokinetics and inhibition of LTB(4)-induced Mac-1 expression of BIIL 284 were characterised in 26 adult patients with RA who were treated with BIIL 284 25 mg, 150 mg, or placebo given once a day for 14 days according to a double blind, randomised, parallel group design.

resultsT(max) of BIIL 315 in plasma (main metabolite and active principle of BIIL 284 in plasma) was achieved about four hours after drug administration, and C(max,ss) and AUC(0-6h,ss) increased in proportion to the dosage. 100% inhibition of LTB(4)-induced MAC-1 expression was reached after two hours (150 mg) or four hours (25 mg), showing a statistically significant difference in comparison with placebo (p<0.005). A longlasting dynamic effect was seen consistently even when plasma concentrations declined to very low values 24 hours after administration. Secondary clinical efficacy end points remained unchanged probably owing to the short duration of treatment. Adverse events (AEs) were reported in 12 patients during the study. No serious AEs or laboratory AEs were seen.

conclusionsBoth the 25 mg and 150 mg doses of BIIL 284 safely and effectively inhibit Mac-1 expression on neutrophils; thus longer treatment with BIIL 284 may result in clinical benefit for patients with RA.

Indexed as

AdolescentAdultAgedAmidinesArea Under CurveArthritis, RheumatoidCarbamatesDouble-Blind MethodFemaleHumansLeukotriene AntagonistsLeukotriene B4Macrophage-1 AntigenMaleMiddle AgedNeutrophilsamelubantAmidinesCarbamatesLeukotriene AntagonistsLeukotriene B4Macrophage-1 Antigen

Identifiers

PMID14722206
PMCPMC1754875
OpenAlexW2161523057

What OpenQuestion holds

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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.