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Transcript
Posters –
Infectious diseases and Vaccines
NAME OF THE PROJECT
NAME OF THE MAIN CONTACT
ORGANISATION NAME
PEPSTAF
Clément Jouanneau
SATT OUEST VALORISATION
Context: The emergence of multi-drug resistance in bacteria seems to be one of the most
issue in human health. In this context, S aureus and Gram negative infections are the
worst case, because of these abilities to bypass immune system and to resist against
many antibiotics.
Issue: The society, both in the community and the hospitals, needs novel antibiotics, and
finding new drugs active on the ESKAPE bacteria has stalled for years because it is
notoriously difficult
Technology
Solution: Scientists have demonstrated that bacterial toxins might be an attractive
starting point for antibacterial drug development. Indeed, bactericidal, cyclic
pseudopeptides were inferred from an S. aureus toxin, and they elicit elevated stability in
human serum. Their activity is against Gram-negative and -positive bacteria without
erythrocyte toxicity; They induce bacterial envelope remodeling with vesicle-like bodies.
The technology developed by research team uses a toxic peptide which have been
chemically modified (cyclization, introduction of analogues), allowing bacterial death
while avoiding hemolytic activity against human cells and we have considerably increased
their half-lifes in human sera.
Our latest results indicated a higher efficiency, compared to Vancomycin, of some
peptides on various resistant strains (IMC of around 1µM)
Customers / Target market
Industry and competitors
Financing need / Commercial
opportunity
IP – Patent situation
Human health:
- Nosocomial diseases
- Multi-drug resistances : S. aureus (MRSA, VISA), E. coli, ESKAPE bacteria
Animal health:
- Bovine Mastitis, a major issue for milk collect
For MRSA market, the main competitors, with their product Linezolid and Cubicin, are
Pfizer and Cubist (Merck).
17% of S.aureus Strains found in hospital are MRSA.
9% of E.coli strains found in hospital are C3G resistant.
Data from WHO global Report on Surveillance AMR 2014
EP patent
Priority data: 10/31/2014
PCT filed on 2015
Future steps / Milestones
Further reading
In vivo Toxicity and efficiency studies are on going
Looking for an industrial partnership:
Clinical trial is the next step to validate the concept in human
Competitive advantages :
- Natural mechanism
-
Reduce production cost (peptide length = 7aa)
Membrane location and action, expecting low resistance levels
Therapeutic Index up to 200
Publications:
“Converting a S.aureus Toxin into effective cyclic pseudopeptide antibiotics” Solecki et al.,
2015, Chemestry & Biology 22, 1-7
Contact person
Clément Jouanneau, Technology Transfer
[email protected]
1/2
Officer,
SATT
Ouest
Valorisation,