Evidence map›Paper›PMID 29075002›Full record

ReviewNature reviews. Drug discovery2018

Drug discovery effectiveness from the standpoint of therapeutic mechanisms and indications.

Hsin-Pei Shih, Xiaodan Zhang, Alex M Aronov

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Drug discovery, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

  1. Trial
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  10. The Future of Drug Delivery.Chemistry of materials : a publication of the American Chemical Society · 2023
    Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Human Genomics and Drug Development.Cold Spring Harbor perspectives in medicine · 2022
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Hsin-Pei ShihGlobal Informatics Group, Modelling & Informatics, Vertex Pharmaceuticals Inc., 50 Northern Avenue, Boston, Massachusetts 02210, USA.
Xiaodan ZhangGlobal Information Services, Vertex Pharmaceuticals Inc., 50 Northern Avenue, Boston, Massachusetts 02210, USA.
Alex M AronovGlobal Informatics Group, Modelling & Informatics, Vertex Pharmaceuticals Inc., 50 Northern Avenue, Boston, Massachusetts 02210, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The productivity of the pharmaceutical industry has been widely discussed in recent years, particularly with regard to concerns that substantial expenditures on research and development have failed to translate into approved drugs. Various analyses of this productivity challenge have focused on aspects such as attrition rates at particular clinical phases or the physicochemical properties of drug candidates, but relatively little attention has been paid to how the industry has performed from the standpoint of the choice of therapeutic mechanisms and their intended indications. This article examines what the pharmaceutical industry has achieved in this respect by analysing comprehensive industry-wide data on the mechanism-indication pairs that have been investigated during the past 20 years. Our findings indicate several points and trends that we hope will be useful in understanding and improving the productivity of the industry, including areas in which the industry has had substantial success or failure and the relative extent of novelty in completed and ongoing projects.

Indexed as

Clinical Trials as TopicDatabases, PharmaceuticalDrug ApprovalDrug DiscoveryDrug IndustryDrugs, InvestigationalEfficiencyHumansDrugs, Investigational

Identifiers

PMID29075002

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.