07 June 2007
Cyprotex Launches New Cloe® Screen Assay to Improve the
Prediction of in vivo Pharmacokinetics
Today, (7th June), Cyprotex announces that it has enhanced the Cloe®
Screen product offering to include an in vitro assay that assesses
the extent to which a compound binds to liver microsomes. When used
in conjunction with microsomal stability data, correction for microsomal
binding can improve the prediction of a compound’s in vivo clearance
and potential for drug-drug interactions. The Cyprotex Cloe® Screen
microsomal binding assay was designed in response to requests from
biotechnology and pharmaceutical companies who work with Cyprotex’
to evaluate potential drug candidates.
Mr. Robert Morrison Atwater, Cyprotex’ Chief Executive Officer,
comments on the launch of the new service ‘Once again Cyprotex
proves itself to be foremost in the provision of in vitro ADMET services.
By offering this service we are adding to our extensive portfolio
of services and reinforcing Cyprotex’ position as a leader within
the industry. Similarly to existing Cloe® Screen assays, the microsomal
binding assay is invaluable in enabling companies to make informed
decisions when selecting compounds to progress further within the
drug discovery process.’
Cyprotex is a specialist provider of ADME data and pharmacokinetic
predictive services. The unique Cloe® Screen technology which
couples robust protocols with state-of-the-art automation enables
Cyprotex to offer an unrivalled combination of high quality, cost
effective data with rapid turnaround. By using data from the Cloe®
Screen microsomal binding assay in conjunction with the existing Cloe®
Screen microsomal stability, a more accurate prediction of the rate
at which a drug is metabolised in vivo is determined than by means
of microsomal stability data alone. The data can also be applied to
improving in vivo drug-drug interaction predictions.
For further information:
Cyprotex PLC
Francesca Sadler, Marketing Manager
Tel: +44 1625 505 100
f.sadler@cyprotex.com
www.cyprotex.com
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