Evidence map›Paper›PMID 31412288›Full record

ReviewDrug discovery today2019

A human-on-a-chip approach to tackling rare diseases.

Camilly P Pires de Mello, John Rumsey, Victoria Slaughter, James J Hickman

Abstract readReview
In one paragraph

Review in Drug discovery today, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Review
  3. Tissue chips as headway model and incitement technology.Synthetic and systems biotechnology · 2025
    Review
  4. Article
  5. Targeted Cancer Therapy-on-A-Chip.Advanced healthcare materials · 2024
    Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Literature Review on Health Emigration in Rare Diseases-A Machine Learning Perspective.International journal of environmental research and public health · 2023
    Review
  11. Optimization of Application-Driven Development ofTissue engineering. Part B, Reviews · 2022
    Review
  12. Review
  13. Review
  14. Review
  15. Organ-on-a-Chip: A New Paradigm for Drug Development.Trends in pharmacological sciences · 2021
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  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

4 authors.

Camilly P Pires de MelloNanoScience Technology Center, University of Central Florida, Orlando, FL 32826, USA.
John RumseyHesperos, Inc., Orlando, FL 32826, USA.
Victoria SlaughterNanoScience Technology Center, University of Central Florida, Orlando, FL 32826, USA.
James J HickmanNanoScience Technology Center, University of Central Florida, Orlando, FL 32826, USA; Hesperos, Inc., Orlando, FL 32826, USA. Electronic address: jhickman@ucf.edu.

Funding

An In Vitro Model of Stem Cell Innervation of MyotubesR01NS050452 · NINDS · UNIVERSITY OF CENTRAL FLORIDA · PI HICKMAN, JAMES J · 2005 to 2020
$6.4M
Human on a chip systems to investigate disease comorbidities common in the aged populationR44AG059511 · NIA · HESPEROS, LLC · PI HICKMAN, JAMES J, SHULER, MICHAEL L · 2018 to 2022
$4.9M
NIA NIH HHS R44 AG059511NINDS NIH HHS R01 NS050452
6 · The paper itself

Abstract

Drug development for rare diseases, classified as diseases with a prevalence of < 200 000 patients, is limited by the high cost of research and low target population. Owing to a lack of representative disease models, research has been challenging for orphan drugs. Human-on-a-chip (HoaC) technology, which models human tissues in interconnected in vitro microfluidic devices, has the potential to lower the cost of preclinical studies and increase the rate of drug approval by introducing human phenotypic models early in the drug discovery process. Advances in HoaC technology can drive a new approach to rare disease research and orphan drug development.

Indexed as

Lab-On-A-Chip DevicesModels, BiologicalDrug ApprovalDrug DiscoveryHumansOrphan Drug ProductionRare Diseases

Identifiers

PMID31412288
PMCPMC6856435

What OpenQuestion holds

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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.