Evidence map›Paper›PMID 25628732›Full record

ReviewJournal of clinical neurology (Seoul, Korea)2015

Oral disease-modifying therapies for multiple sclerosis.

Woojun Kim, Manuella Edler Zandoná, Su-Hyun Kim, Ho Jin Kim

Abstract readReview
In one paragraph

Review in Journal of clinical neurology (Seoul, Korea), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Drug Repurposing: A Leading Strategy for New Threats and Targets.ACS pharmacology & translational science · 2024
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. A comprehensive review on the treatment approaches of multiple sclerosis: currently and in the future.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2019
    Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Sphingosine-1-phosphate inhibits IL-1-induced expression of C-C motif ligand 5 via c-Fos-dependent suppression of IFN-β amplification loop.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  14. Article
  15. Article
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

4 authors.

Woojun KimDepartment of Neurology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Manuella Edler ZandonáPontifical Catholic University of Rio Grande do Sul, Science Without Borders, Porto Alegre, Brazil. ; Department of Neurology, Research Institute and Hospital of National Cancer Center, Goyang, Korea.
Su-Hyun KimDepartment of Neurology, Research Institute and Hospital of National Cancer Center, Goyang, Korea.
Ho Jin KimDepartment of Neurology, Research Institute and Hospital of National Cancer Center, Goyang, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classical multiple sclerosis (MS) treatments using first-line injectable drugs, although widely applied, remain a major concern in terms of therapeutic adherence and efficacy. New oral drugs recently approved for MS treatment represent significant advances in therapy. The oral route of administration clearly promotes patient satisfaction and increases therapeutic compliance. However, these drugs may also have safety and tolerability issues, and a thorough analysis of the risks and benefits is required. Three oral drugs have been approved by regulatory agencies for MS treatment: fingolimod, teriflunomide, and dimethyl fumarate. This article reviews the mechanisms of action, safety, and efficacy of these drugs and two other drugs that have yielded positive results in phase III trials: cladribine and laquinimod.

Indexed as

clinical trialmultiple sclerosisoral drugtreatment

Identifiers

PMID25628732
PMCPMC4302185

What OpenQuestion holds

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Registered trials

None linked

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.