CIT launches LeadScreen services for drug candidate selection
11 April 2011
French contract research organization CIT has announced a new
range of services for companies developing new drugs.
The services, grouped under the name LeadScreen, offer an
array of tests designed to give an early evaluation of safety of
drugs thought to have development potential.
Currently, around 20% of candidate drugs fail during standard
regulatory non-clinical studies, too often due to late
identification of toxicological effects.
CIT says that using its LeadScreen, the early detection of
potential toxicity can significantly increase the chances of success
when the candidate drug goes through the later stages of
non-clinical development. The speed, competitive price and efficacy
of LeadScreen offers the ability to reduce considerably the
financial cost and time associated with standard drug development
practices.
LeadScreen services comprise:
- LeadScreen Tox allows more precise selection of the future
drug candidate. Using CIT’s expertise in toxicology, genomics
and biomarker analysis, LeadScreen Tox offers a multi-criteria
toxicology study that can be critical in deciding which
pre-selected molecules should be pursued. In a four-day
predictive study, LeadScreen Tox combines the clinic (daily
clinical examinations), clinical biology, histopathology,
toxico-genomics, biomarker identification, in vivo micronuclei
and toxico-kinetics.
- LeadScreen Genotox allows the evaluation of the genotoxicity
of candidates using BlueScreen tests, mini-Ames and
mini-micronucleus.
- LeadScreen Safety allows the evaluation of pharmacological
safety parameters, such as QT prolongation and other
cardiovascular parameters in vivo.
- LeadScreen PK allows the definition of in vivo half-life and
bioavailability.
- devTox and cardioTox: LeadScreen also includes tests offered
by CIT’s Wisconsin-based partner, Stemina Biomarker Discovery.
These use metabolomics and embryonic human stem cells to
identify biomarkers for developmental (devTox) and cardiac
toxicity (cardioTox).
“CIT’s LeadScreen enables our customers to perform research on
candidate molecules included in development programs prior to their
entry into the more advanced stages of pre-clinical research — and
it provides pertinent data that make it easier to identify candidate
drugs that have the best safety profile,” said Sophie Baratte, CEO
at CIT. “Moreover, these data also allow clients better to define
and conduct regulatory studies, while increasing the probability of
bringing a candidate drug to market. LeadScreen is a great
complement to the wide ranging safety evaluation services that CIT
carries out during regulatory pre-clinical research.”