Evidence map›Paper›PMID 34293063›Full record

ReviewPLoS pathogens2021

Development of emodepside as a possible adulticidal treatment for human onchocerciasis-The fruit of a successful industrial-academic collaboration.

Jürgen Krücken, Lindy Holden-Dye, Jennifer Keiser, Roger K Prichard, Simon Townson, Benjamin L Makepeace, Marc P Hübner, Steffen R Hahnel, Ivan Scandale, Achim Harder and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in PLoS pathogens, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 9% of its field
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

21 citing papers in PubMed, 48 citations in OpenAlex.

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  12. Diethylcarbamazine elicits CaAntimicrobial agents and chemotherapy · 2023
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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

11 authors at 9 institutions in 5 countries.

Jürgen KrückenInstitute for Parasitology and Tropical Veterinary Medicine, Freie Universität Berlin, Berlin, Germany.ORCID 0000-0002-2842-8100
Lindy Holden-DyeSchool of Biological Sciences, Institute for Life Sciences, University of Southampton, Southampton, United Kingdom.ORCID 0000-0002-9704-1217
Jennifer KeiserDepartment of Medical Parasitology and Infection Biology, Swiss Tropical and Public Health Institute, Basel, Switzerland.
Roger K PrichardInstitute of Parasitology, McGill University, Sainte Anne-de-Bellevue, Quebec, Canada.
Simon TownsonThe Griffin Institute, Northwick Park and St. Mark's Hospital, Harrow, United Kingdom.ORCID 0000-0002-2561-6579
Benjamin L MakepeaceInstitute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, United Kingdom.ORCID 0000-0002-6100-6727
Marc P HübnerInstitute for Medical Microbiology, Immunology and Parasitology, University Hospital Bonn, Bonn, Germany.ORCID 0000-0001-8885-418X
Steffen R HahnelElanco Animal Health, Research & Exploratory Development, Monheim, Germany.ORCID 0000-0001-8848-0691
Ivan ScandaleDrugs for Neglected Disease initiative, Geneva, Switzerland.ORCID 0000-0003-4242-9289
Achim HarderIndependent Researcher, Cologne, Germany.ORCID 0000-0002-5722-4334
Daniel KulkeDepartment of Biomedical Sciences, Iowa State University, Ames, Iowa, United States of America.ORCID 0000-0002-7373-6612
Drugs for Neglected Diseases Initiative · CHFreie Universität Berlin · DEIowa State University · USMcGill University · CASt Mark's Hospital · GBSwiss Tropical and Public Health Institute · CHUniversity Hospital Bonn · DEUniversity of Liverpool · GBUniversity of Southampton · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current mass drug administration (MDA) programs for the treatment of human river blindness (onchocerciasis) caused by the filarial worm Onchocerca volvulus rely on ivermectin, an anthelmintic originally developed for animal health. These treatments are primarily directed against migrating microfilariae and also suppress fecundity for several months, but fail to eliminate adult O. volvulus. Therefore, elimination programs need time frames of decades, well exceeding the life span of adult worms. The situation is worsened by decreased ivermectin efficacy after long-term therapy. To improve treatment options against onchocerciasis, a drug development candidate should ideally kill or irreversibly sterilize adult worms. Emodepside is a broad-spectrum anthelmintic used for the treatment of parasitic nematodes in cats and dogs (Profender and Procox). Our current knowledge of the pharmacology of emodepside is the result of more than 2 decades of intensive collaborative research between academia and the pharmaceutical industry. Emodepside has a novel mode of action with a broad spectrum of activity, including against extraintestinal nematode stages such as migrating larvae or macrofilariae. Therefore, emodepside is considered to be among the most promising candidates for evaluation as an adulticide treatment against onchocerciasis. Consequently, in 2014, Bayer and the Drugs for Neglected Diseases initiative (DNDi) started a collaboration to develop emodepside for the treatment of patients suffering from the disease. Macrofilaricidal activity has been demonstrated in various models, including Onchocerca ochengi in cattle, the parasite most closely related to O. volvulus. Emodepside has now successfully passed Phase I clinical trials, and a Phase II study is planned. This Bayer-DNDi partnership is an outstanding example of "One World Health," in which experience gained in veterinary science and drug development is translated to human health and leads to improved tools to combat neglected tropical diseases (NTDs) and shorten development pathways and timelines in an otherwise neglected area.

Indexed as

Antiparasitic AgentsDepsipeptidesDrug DevelopmentHumansOnchocerciasisAntiparasitic AgentsDepsipeptidesemodepside

Identifiers

PMID34293063
PMCPMC8297762
OpenAlexW3184579517

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.