Evidence map›Paper›PMID 20689698›Full record

ReviewDrug design, development and therapy2010

Identification of targets and new developments in the treatment of multiple sclerosis--focus on cladribine.

Clemens Warnke, Heinz Wiendl, Hans-Peter Hartung, Olaf Stüve, Bernd C Kieseier

Registry-linked trialAbstract readReview
In one paragraph

Review in Drug design, development and therapy, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04178005 (Cladribine Tablets After Treatment With Natalizumab), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

NCT04178005 phase4active not recruitingnot on this mapstarted 2020, after this paper: background citation

Cladribine Tablets After Treatment With Natalizumab (CLADRINA)

TypeinterventionalSponsorUniversity of Texas Southwestern Medical CenterRan2020 to 2026Enrolled40ConditionsMultiple SclerosisArmsCladribine
3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
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  8. Review
  9. 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

5 authors.

Clemens WarnkeDepartment of Neurology, Heinrich-Heine University Düsseldorf, Germany.
Heinz Wiendl
Hans-Peter Hartung
Olaf Stüve
Bernd C Kieseier

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Orally available disease-modifying drugs for relapsing-remitting multiple sclerosis (MS) represent an unmet need for this chronic and debilitating disease. Among 5 currently investigated drugs at phase 3 clinical stage, promising efficacy data for fingolimod and oral cladribine have recently been published. However, benefits need to be weighed against the risks to define the role of these compounds within current treatment regimens. In this review, data on the efficacy of a promising compound, oral cladribine, are discussed and balanced with known and anticipated risks in a postmarketing era, and finally gives an outlook on the potential place of this drug in treatment algorithms for MS in the future.

Indexed as

Drug Delivery SystemsAdministration, OralAnimalsCladribineClinical Trials as TopicDrug DesignFingolimod HydrochlorideHumansImmunosuppressive AgentsMultiple Sclerosis, Relapsing-RemittingPropylene GlycolsSphingosineCladribineFingolimod HydrochlorideImmunosuppressive AgentsPropylene GlycolsSphingosineimmunosuppressantoral drugsrisk–benefitsafety

Identifiers

PMID20689698
PMCPMC2915536

What OpenQuestion holds

Textmetadata
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.