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Biotie Therapies Oyj was a and company that was acquired by Acorda Therapeutics in January 2016. The company's research and development was focused on drugs for neurodegenerative and psychiatric disorders like Parkinson's disease, Alzheimer's disease and other cognitive disorders, alcohol and and post traumatic stress disorder, and and . The company's headquarters is in , , and it is listed on Helsinki.


Overview
Biotie Therapies was formed in the merger of Biotie Therapies Corp. (incorporated in 1998), Oy Contral Pharma Ltd and Carbion Inc in the year 2002. In 2008, Biotie Therapies acquired the German pharmaceutical discovery and development company Elbion GmbH in . In 2010 Biotie Therapies all preclinical assets were transferred into a new company, biocrea GmbH, in which Biotie become a minority shareholder. In 2011, Biotie acquired a pharmaceutical company, Synosia.

The company has partnering agreements with and UCB. Biotie Therapies Oyj Company Description Business Week

In January 2016, Acorda Therapeutics acquired Biotie Therapies for $363 million.


Product pipeline
Selincro ()alcohol dependenceEU marketing authorization received
Tozadenant SYN115Parkinson's diseaseUCBPhase III clinical trials to start 2015
VAP-1 inflammatory diseases-Phase I clinical trials ready, seeking partner
SYN120AD, cognitive disorders-Phase I clinical trials ready, seeking partner
SYN117, cocaine dependencyNIDAPTSD: Phase II clinical trials, results
Cocaine dependency: Phase II clinical trials, in progress
Ronomilast-Phase I clinical trials ready, seeking partner
SYN118Movement disorderUCBPhase II clinical trials, terminated [2] Stock Exchange release 23 November 2011
Sources:


Selincro (nalmefene)
The company's most advanced product, , for the treatment of . Biotie's partner H. Lundbeck A/S received European marketing authorization from the European Commission on 28 February 2013. Lundbeck expects to launch Selincro in its first markets in the middle of 2013.

Studies have shown, that has the ability to significantly limit both the patient's average alcohol intake and the number of days with an intake above five units of alcohol. The drug works by removing the patient's desire to drink more, thereby controlling and limiting the intake of alcohol. The drug will be used in tablet form, and taken only according to need. According to the company, this is a novel approach for alcohol dependency treatment; existing treatments are aimed at keeping the patient from drinking and the drugs have to be taken continuously over a longer period of time. Lundbeck announces start of new phase III clinical trials with nalmefene STOCK EXCHANGE RELEASE 15 December 2008 at 9.30 a.m Balanced CNS and inflammation product pipeline Company website 2008-03-15


Tozadenant
SYN115, also called tozadenant, was developed as a potential treatment for Parkinson's disease or other . It was an orally administered, potent and [selective inhibitor of the adenosine A2A receptor.

In January 2016, the company was acquired by Acorda Therapeutics, for . In November 2017, the company announced discontinuation of the agent following the death of 5 patients enrolled in the tozadenant Phase III trial from and associated severe adverse events possibly related to tozadenant.


VAP-1
Vascular Adhesion Protein-1 (VAP-1) monoclonal antibody - intended for treatment of inflammatory diseases, is currently in Phase I clinical trials with rheumatoid arthritis patients. According to the company, inhibiting VAP-1 reduces by regulating the migration of , or white blood cells, to inflamed tissues. Pathological accumulation of white blood cells in tissue is a common feature in many autoimmune diseases, such as rheumatoid arthritis, ulcerative colitis, and .


Nepicastat
SYN117 also called nepicastat is a treatment for cocaine dependency and post traumatic stress disorder (PTSD). It is orally administered, potent and selective inhibitor of the enzyme dopamine β-hydroxylase (DBH).


Ronomilast
Ronomilast is a PDE4 inhibitor for chronic inflammatory disorders. It is a small molecule phosphodiesterase-4 inhibitor (PDE4). The product is developed for the treatment of chronic obstructive pulmonary disease (COPD). Data from pre-clinical and early clinical trials indicates that the product has a good safety profile. Biotie is in the process of planning a Phase 2 trial in COPD patients and also seeking a partner for late-stage development of ronomilast.


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