Summary:
The READ-UP project aims at identifying antimalarial drug candidates (one
candidate and two back-ups). The project will begin with a hit identified in the
first series, enlarging it, and designing other series through the different
steps of drug discovery and hit-to-lead optimisation from the pilot scale
production towards pre-clinical studies.
Artemisinin, the natural antimalarial product, and its derivatives are
increasingly important in the treatment of drug-resistant malaria as they are
the most potent antimalarials available, rapidly killing all blood stages of the
malaria parasite. Artemisinins contain an endoperoxide bridge which plays a key
role in the antimalarial activity with a mode of action starting from radical
transient species initiated by the cleavage of this bridge. The READ-UP project
starts from the unique mode of action of artemisinins to develop a completely
new approach: initiate radical transient species within the parasitised red
blood cell in such a way that no endoperoxide bridge is required.
Background:
Malaria remains one of the most devastating diseases of the developing world,
causing more than 1 million deaths and 300-500 million clinical cases each year.
Although four Plasmodium species infect humans (P. falciparum (P.
f.), P. vivax, P. ovale and P. malariae), most deaths are caused by the
severe complications of P. f. malaria. Malaria-related morbidity and
mortality are increasing, mainly as a consequence of drug resistance as observed
with the two most widely used antimalarial drugs: chloroquine and
sulfadoxine-pyrimethamine. To combat malaria, new drugs are urgently needed.
In this context, the READ-UP project brings together public organisations and
SMEs to drive a research project aimed at identifying a new drug candidate for
malaria. Starting from one series with antimalarial activity, which was created
by a public laboratory of the consortium using a new approach, the project,
coordinated by a pharmaceutical SME, will realise hit-to-lead optimisation
through molecular modelling, testing of new chemical entities in vitro and in
vivo and pharmacological, pharmacokinetics, toxicological and mechanisms
studies.
Aim:
Following the drug discovery process until the pilot-scale production, the
objective is to propose one antimalarial drug candidate with two back-ups for
further pre-clinical studies.
Expected results:
An initial series of new stable compounds has been developed by UPS. In a
first synthetic series, several compounds presented anti-plasmodial properties
and preliminary in vitro and in vivo studies led to the
identification of one hit. Based on the excellent in vitro and in
vivo results already obtained, the READ-UP project will develop new
structural analogues using the same innovative approach. The in vitro and in
vivo results obtained will be further improved by the application of
optimisation techniques, through the ‘Drug Discovery’ process that the READ-UP
partners will implement. The project aims at enlarging this first series and
designing other series to identify new antimalarial drug candidates (one drug
candidate and two back-ups) through the different steps of drug discovery and
hit optimisation. Moreover, the READ-UP innovative strategy should allow
designing chemically stable compounds, which may have a longer duration of
action in vivo.
Potential applications:
Application of READ-UP scientific breakthroughs into approved new
medicines.
Coordinator:
Serge Petit Idéalp’ Pharma/IDEALP Bât. CEI – 66 Bd Niels Bohr - BP 2132 69603 Villeurbanne Cedex France Tel: +33 4 37 48 88 00 Fax: +33 4 78 93 56 53 Website: http://www.idealp-pharma.com
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Partners:
| Nº |
Principal
Scientific
Participants |
Official Address |
Other Information |
2
| Françoise Nepveu
| Université Paul Sabatier and Institut de Recherche pour le Développement Laboratoire ‘Pharmacochimie des Substances Naturelles et Pharmacophores Redox’ Université Paul Sabatier, Toulouse 3 Faculté de Pharmacie, 31 062 Toulouse Cedex 9 France
| Tel: +33 (0)5 61 55 66 13 Fax: +33 (0)5 61 55 64 70 E-mail: nepveu@cict.fr Website: http://www.ups-tlse.fr
| 3
| Paolo Arese
| Dipartimento Di Genetica, Biologia E Biochimica, Universita Di Torino Via Santena 6 bis 10126 Torino Italy
| Tel: +39 011 6706686 Fax: +39 011 6706590 E-mail: paolo.arese@unito.it
| 4
| Livia Vivas
| London University London School of Hygiene & Tropical Medicine University of London Department of Hygiene and Tropical Diseases Keppel Street UK-London WC1E 7HT | Tel: +44 (0)02-7927 2345 Fax: +44 (0)02-7637 4314 E-mail: livia.vivas@lshtm.ac.uk Website: http://www.lshtm.ac.uk
| 5
| Leonardo Basco
| Organisation de Coordination pour la lutte contre les Endémies en Afrique Centrale OCEAC-IRD BP 288 Yaoundé Cameroun
| Tel: +237 23 2232/237786 Fax: +237 23 0061 E-mail: leonardo.basco@ibaic.u-psud.fr
| 6
| Laurence Touchard-Nicod
| ACIES 69, rue de la République 69002 Lyon France
| Tel: +33 (0)4 78 92 40 00 Fax: +33 (0)4 78 92 40 01 E-mail: readup@acies.fr Website: http://www.acies.fr
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