Laquinimod * On May 23, the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) reaffirmed its negative opinion on the market application for laquinimod (Nerventra®) * CHMP confirmed that the risks observed in animal studies do not prevent a registration for treatment in humans * The ongoing US pivotal clinical study CONCERTO is continuing according to plan. The results are expected in 2016 Tasquinimod * The Phase III study 10TASQ10 is proceeding according to plan ANYARA * Development program for further clinical development outlined in collaboration with regulatory authorities * All project activities will be put on hold until further notice Paquinimod (57-57) * In June 2014, data related to the drug candidate paquinimod for the treatment of systemic sclerosis was presented at the scientific conference "EULAR Annual European Congress of Rheumatology" ISI * Expansion of the patent portfolio * CD selection expected in 2015 Financial summary MSEK April - June January - June Full Year 2014 2013 2014 2013 2013 -------------------------------------------------------------- Net sales 2.7 2.5 4.9 5.0 116.0 Operating loss -57.9 -79.5 -117.2 -156.5 -209.0 Loss for the period -57.7 -81.2 -117.9 -159.2 -212.1 Loss per share (SEK) -0.77 -1.08 -1.57 -2.18 -2.87 For further information, please contact: Tomas Leanderson, President and Active Biotech AB CEO (Corp. Reg. No. 556223-9227) Tel: +46 (0)46 19 20 95 Box 724, SE-220 07 Lund Tel: +46 (0)46 19 20 00 Hans Kolam, CFO Fax: +46 (0)46 19 11 00 Tel: +46 (0)46 19 20 44 The report is also available at www.activebiotech.com [HUG#1846988]
Active Biotech AB Interim report January-June 2014
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