Theranexus, a clinical-stage biopharmaceutical company, announced today that the first patient has been recruited in the study entitled “safety and efficacy of THN102 on sleepiness in narcolepsy patients” (NCT02821715), a phase II clinical study evaluating the efficacy and tolerance of THN102 in the treatment of excessive daytime sleepiness associated with narcolepsy in adult patients. This double-blind study will compare two different doses of THN102 with an active comparator, modafinil - the standard of care drug for treating sleepiness in narcolepsy patients. The protocol is being conducted according to a design referred to as cross-over: a study design in which each patient will receive all of the proposed treatments over successive treatment periods. The main objective of the study is to show a decrease in sleepiness as measured by the Epworth Sleepiness Scale (ESS) - the reference scale for measuring sleepiness in narcolepsy patients. This study, which is being financed in part by the French National Research Agency (ANR, project NarConX), will enroll in total 48 patients at three French centres, those being Montpellier Regional University Hospital (Professor Yves Dauvilliers – Principal investigator for the study), the Paris public hospital organisation APHP (Dr Isabelle Arnulf) and Lille Regional University Hospital (Dr Christelle Charley-Monaca).
Professor Yves Dauvilliers (Regional University Hospital in Montpellier, France) stated: “This new approach developed by Theranexus carries with it a real sense of hope for a better answer to the ever-weighty medical needs in narcolepsy. If we confirm in patients the data obtained in disease models as well as in healthy, sleep-deprived volunteers, then THN102 will represent an interesting therapeutic option for treating our patients once it is on the market. »
“Launching this phase II study with THN102 underscores our commitment at Theranexus to improving the life of patients suffering from narcolepsy,” declared Franck Mouthon, the President of Theranexus. “We see the completion of this study as a possibility to give a real-life demonstration of the ability of our technology to generate new and more effective drugs for patients suffering from neurological or psychiatric illnesses,” he added.
View source version on businesswire.com: http://www.businesswire.com/news/home/20161027005096/en/Business Wire
Last updated on: 27/10/2016
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