Evidence map›Paper›PMID 28139658›Full record

ArticleNature communications2017

SC83288 is a clinical development candidate for the treatment of severe malaria.

Stefano Pegoraro, Maëlle Duffey, Thomas D Otto, Yulin Wang, Roman Rösemann, Roland Baumgartner, Stefanie K Fehler, Leonardo Lucantoni, Vicky M Avery, Alicia Moreno-Sabater and 5 more

Erratum issuedAbstract read
In one paragraph

Article in Nature communications, 2017. 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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Antimalarial drug discovery: progress and approaches.Nature reviews. Drug discovery · 2023
    Review
  3. Article
  4. Humanized Mice as a Tool to Study Sepsis-More Than Meets the Eye.International journal of molecular sciences · 2021
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Stefano Pegoraro4SC AG, Am Klopferspitz 19a, 82152 Martinsried, Germany.
Maëlle DuffeyDepartment of Infectious Diseases, Parasitology, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 324, 69120 Heidelberg, Germany.
Thomas D OttoParasite Genomics, Wellcome Trust Sanger Institute, Wellcome Genome Campus, Hinxton CB10 1SA, UK.ORCID 0000-0002-1246-7404
Yulin WangDepartment of Infectious Diseases, Parasitology, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 324, 69120 Heidelberg, Germany.
Roman Rösemann4SC Discovery GmbH, Am Klopferspitz 19a, 82152 Martinsried, Germany.
Roland Baumgartner4SC AG, Am Klopferspitz 19a, 82152 Martinsried, Germany.
Stefanie K Fehler4SC AG, Am Klopferspitz 19a, 82152 Martinsried, Germany.
Leonardo LucantoniEskitis Institute for Drug Discovery, Griffith University, Don Young, Nathan Queensland 4111, Australia.
Vicky M AveryEskitis Institute for Drug Discovery, Griffith University, Don Young, Nathan Queensland 4111, Australia.ORCID 0000-0003-4914-2299
Alicia Moreno-SabaterSorbonne Universités, UPMC Univ Paris 06, INSERM U1135, CNRS ERL 8255, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), 91 Bd de l'hôpital, F-75013 Paris, France.
Dominique MazierSorbonne Universités, UPMC Univ Paris 06, INSERM U1135, CNRS ERL 8255, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), 91 Bd de l'hôpital, F-75013 Paris, France.
Henri J VialDynamique des Interactions Membranaires Normales et Pathologiques, CNRS UMR 5235, Université Montpellier II, cc107, Place Eugène Bataillon, 34095 Montpellier, France.
Stefan Strobl4SC Discovery GmbH, Am Klopferspitz 19a, 82152 Martinsried, Germany.
Cecilia P SanchezDepartment of Infectious Diseases, Parasitology, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 324, 69120 Heidelberg, Germany.
Michael LanzerDepartment of Infectious Diseases, Parasitology, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 324, 69120 Heidelberg, Germany.ORCID 0000-0002-0220-6526

Funding

Wellcome Trust
6 · The paper itself

Abstract

Severe malaria is a life-threatening complication of an infection with the protozoan parasite Plasmodium falciparum, which requires immediate treatment. Safety and efficacy concerns with currently used drugs accentuate the need for new chemotherapeutic options against severe malaria. Here we describe a medicinal chemistry program starting from amicarbalide that led to two compounds with optimized pharmacological and antiparasitic properties. SC81458 and the clinical development candidate, SC83288, are fast-acting compounds that can cure a P. falciparum infection in a humanized NOD/SCID mouse model system. Detailed preclinical pharmacokinetic and toxicological studies reveal no observable drawbacks. Ultra-deep sequencing of resistant parasites identifies the sarco/endoplasmic reticulum Ca

Indexed as

Acute DiseaseAnimalsAntimalarialsCalcium-Transporting ATPasesDisease Models, AnimalDrug ResistanceEndoplasmic ReticulumGene ExpressionHumansInhibitory Concentration 50Ion TransportMalaria, FalciparumMaleMiceMice, Inbred NODMice, SCIDAntimalarialsATP6 protein, Plasmodium falciparumCalcium-Transporting ATPases

Identifiers

PMID28139658
PMCPMC5290327

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.