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Huntington’s Disease (HD) is a neurodegenerative disorder that gives rise to progressive neuronal dysfunction and cell death, that affects muscle coordination and leads to cognitive decline. > More
The PADDINGTON project supports the development of a series of pharmacodynamic markers to explore potential disease-modifying properties of a potential new drug for Huntington’s Disease treatment, ultimately striving to use the compound to delay disability. > More
PADDINGTON Project European Seventh Framework Programme Project The aim of the PADDINGTON project is to develop and ascertain clinical feasibility of a range of pharmacodynamic markers for the clinical development of SEN0014196, a novel and selective Siena Biotech compound with disease-modifying potential in Huntington’s Disease. SEN0014196 enjoys Orphan Status in the EU and in the US and is currently in Phase II clinical development. |
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News and Events 2012 UK Site Investigators’ Meeting, 30 April-1 May, 2012, The Studio, Birmingham (UK) As per the World Health Organization (WHO) regulations, Siena Biotech SpA (Partner 1) has received approval for the name “selisistat” as the official International Nonproprietary Name (INN) to designate the SEN0014196 compound. Clinical Trials WP1: PADDINGTON Clinical StudyA multi-centre, double-blind, placebo-controlled, ascending multiple oral dose, sequential group study conducted at two dose levels of SEN0014196 across six EU sites. > More WP2: Imaging Clinical StudyA multi-centre study across four sites in the EU to expand MRI technique as a biomarker for SEN0014196 clinical studies. > More |
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