OctoPlus announces that Locteron interim Phase IIb data have been accepted for oral and poster presentations at International Liver Congress in April
(Thomson Reuters ONE) - OctoPlus N.V. ("OctoPlus" or "the Company") (Euronext: OCTO) announces todaythat its licensee Biolex Therapeutics (see separate Biolex press release onwww.biolex.com) has been accepted to present interim results from two ongoingPhase IIb studies with Locteron® at the 45th Liver Congress on 14 -18 April2010 in Vienna, Austria.Simon Sturge, CEO of OctoPlus, says: "We are delighted that the interim data forLocteron have been one of few to be selected for an oral presentation at thisprestigious conference. We look forward to seeing the data and believe that thisis very good news for the future of Locteron." * Biolex will present interim results after 12 weeks of treatment from its two Phase IIb studies for Locteron versus PEG-Intron® at the International Liver Congress in April, organised by the European Association for the Study of the Liver (EASL). * The objectives of the two Phase IIb trials are to demonstrate viral kinetics and response that is at least equivalent to the PEG-Intron control, while also achieving at least a 50% reduction in flu-like adverse events. * The data have been accepted for both oral and poster presentations. Under the strict rules of the conference, the results are currently embargoed until publication at the conference. * The "SELECT-2" Phase IIb study is being conducted in the United States and Europe in 116 treatment-na?, genotype-1, chronic hepatitis C patients. Patients have been randomised into one of four dosing cohorts, the 320, 480 or 640 µg dose of Locteron (administered once every two weeks) or a control arm consisting of PEG-Intron (administered every week), with all patients receiving weight-based ribavirin. Patients will be treated for 48 weeks and will be followed for an additional 24 weeks to determine the sustained virologic response (SVR) rate. The SELECT-2 Phase IIb clinical study started in April 2009, and patient enrollment was completed in June 2009. * The second component of the planned Phase IIb trial program for Locteron, the "480 STUDY", is designed to provide clinical experience with the same Locteron configuration that is planned for use in Phase III trials. The 480 STUDY was also initiated last year, is being conducted in Europe and Israel, and will include at least 72 treatment-na? hepatitis C patients with the genotype-1 variant of the virus. * Locteron's expected product profile was tested by Biolex in extensive market research in the first half of 2009, and the research results suggested that the potential tolerability and dosing convenience advantages of Locteron support a substantial commercial opportunity. It is estimated that worldwide sales of interferon products for the treatment of hepatitis C will approach US$6 billion by 2016.Under its agreement with Biolex, OctoPlus is eligible to: * Milestone payments which may exceed US$ 135 million * Royalties on net product sales. * An equity stake in Biolex.For further information, please contact:Rianne Roukema, Corporate Communications: telephone number +31 (71) 524 1071, orsend an e-mail to Investor Relations at IR(at)octoplus.nl.About LocteronLocteron is a controlled release formulation of interferon alpha for thetreatment of chronic hepatitis C. Locteron combines OctoPlus' controlled releasedrug delivery technology PolyActive® with Biolex' interferon alpha and is themost advanced product in clinical development incorporating one of OctoPlus'proprietary drug delivery technologies. OctoPlus licensed its commercial rightsto Locteron exclusively to Biolex in October 2008.About OctoPlusOctoPlus is a drug delivery service company committed to the creation ofimproved pharmaceutical products that are based on OctoPlus' proprietary drugdelivery technologies and have fewer side effects, improved patient convenienceand a better efficacy/safety balance than existing therapies. OctoPlus focuseson the development of long-acting, controlled release versions of known proteintherapeutics, other drugs, and vaccines on behalf of its clients.The clinically most advanced product incorporating our technology is BiolexTherapeutics' lead product Locteron®, a controlled release formulation ofinterferon alpha for the treatment of chronic hepatitis C. OctoPlus licensedLocteron exclusively to Biolex in October 2008. Locteron is being manufacturedfor Biolex by OctoPlus and is currently in Phase IIb clinical studies.In addition, OctoPlus is a leading European provider of advanced drugformulation and clinical scale manufacturing services to the pharmaceutical andbiotechnology industries, with a focus on difficult-to-formulate activepharmaceutical ingredients.OctoPlus is listed on Euronext Amsterdam by NYSE Euronext under the symbol OCTO.For more information about OctoPlus, please visit our website www.octoplus.nl.This document may contain certain forward-looking statements relating to thebusiness, financial performance and results of OctoPlus and the industry inwhich it operates. These statements are based on OctoPlus' current plans,estimates and projections, as well as its expectations of external conditionsand events. In particular the words "expect", "anticipate", "predict","estimate", "project", "plan", "may", "should", "would", "will", "intend","believe" and similar expressions are intended to identify forward-lookingstatements. We caution investors that a number of important factors, and theinherent risks and uncertainties that such statements involve, could causeactual results or outcomes to differ materially from those expressed in anyforward-looking statements. In the event of any inconsistency between an Englishversion and a Dutch version of this document, the English version will prevailover the Dutch version.[HUG#1382575] Click here for the press release in PDF: http://hugin.info/137076/R/1382575/341472.pdf
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