Evidence map›Paper›PMID 29783676›Full record

ReviewToxins2018

The Expanding Therapeutic Utility of Botulinum Neurotoxins.

Elena Fonfria, Jacquie Maignel, Stephane Lezmi, Vincent Martin, Andrew Splevins, Saif Shubber, Mikhail Kalinichev, Keith Foster, Philippe Picaut, Johannes Krupp

Abstract readReview
In one paragraph

Review in Toxins, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 1 pooled it
–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

72 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. The Degradation of Botulinum Neurotoxin Light Chains Using PROTACs.International journal of molecular sciences · 2024
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. TRPV1BMC immunology · 2023
    Article
  20. Article

12 more citing papers are in PubMed but not listed here.

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

10 authors.

Elena FonfriaIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon, Oxfordshire OX14 4RY, UK. elena.fonfria@ipsen.com.
Jacquie MaignelIpsen Innovation, 5 Avenue du Canada, 91940 Les Ulis, France. jacquie.maignel@ipsen.com.
Stephane LezmiIpsen Innovation, 5 Avenue du Canada, 91940 Les Ulis, France. stephane.lezmi@ipsen.com.
Vincent MartinIpsen Innovation, 5 Avenue du Canada, 91940 Les Ulis, France. vincent.martin@ipsen.com.
Andrew SplevinsIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon, Oxfordshire OX14 4RY, UK. andrew.splevins@ipsen.com.
Saif ShubberIpsen Biopharm Ltd., Wrexham Industrial Estate, 9 Ash Road, Wrexham LL13 9UF, UK. saif.shubber@ipsen.com.
Mikhail KalinichevIpsen Innovation, 5 Avenue du Canada, 91940 Les Ulis, France. mikhail.kalinichev@ipsen.com.
Keith FosterIpsen Bioinnovation, 102 Park Drive, Milton Park, Abingdon, Oxfordshire OX14 4RY, UK. keith.foster@ipsen.com.
Philippe PicautIpsen Bioscience, 650 Kendall Street, Cambridge, MA 02142, USA. philippe.picaut@ipsen.com.
Johannes KruppIpsen Innovation, 5 Avenue du Canada, 91940 Les Ulis, France. johannes.krupp@ipsen.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Botulinum neurotoxin (BoNT) is a major therapeutic agent that is licensed in neurological indications, such as dystonia and spasticity. The BoNT family, which is produced in nature by clostridial bacteria, comprises several pharmacologically distinct proteins with distinct properties. In this review, we present an overview of the current therapeutic landscape and explore the diversity of BoNT proteins as future therapeutics. In recent years, novel indications have emerged in the fields of pain, migraine, overactive bladder, osteoarthritis, and wound healing. The study of biological effects distal to the injection site could provide future opportunities for disease-tailored BoNT therapies. However, there are some challenges in the pharmaceutical development of BoNTs, such as liquid and slow-release BoNT formulations; and, transdermal, transurothelial, and transepithelial delivery. Innovative approaches in the areas of formulation and delivery, together with highly sensitive analytical tools, will be key for the success of next generation BoNT clinical products.

Indexed as

AnimalsBotulinum ToxinsDrug Administration RoutesDrug CompoundingHumansNeurotoxinsPeripheral Nervous System AgentsSerogroupBotulinum ToxinsNeurotoxinsPeripheral Nervous System Agentsdeliveryformulationnew indications

Identifiers

PMID29783676
PMCPMC5983264

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.