LUND, SWEDEN--(Marketwire - April 26, 2012) -
* Laquinimod - submission of application for regulatory approval in the EU planned for second half of 2012 - Phase III data presented at the Annual Meeting of the American Academy of Neurology (AAN) * TASQ - a Phase I investigator-sponsored clinical trial is under way - enrolment of patients to Phase III study proceeding according to schedule * ANYARA - Phase III trial continuing according to plan * 57-57 - a clinical trial in systemic sclerosis/scleroderma in progress * ISI - project is proceeding as planned * Net sales SEK 2.6 M (2.7) * Operating loss SEK 100.7 M (loss: 70.9) * Net loss SEK 99.0 M (loss: 69.3 ) * Loss per share for the period was SEK 1.44 (loss: 1.02)
This report is also available at www.activebiotech.com
Active Biotech AB Interim report January - March 2012: http://hugin.info/1002/R/1605995/508858.pdf
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Source: Active Biotech via Thomson Reuters ONE [HUG#1605995]
For further information, please contact:
Tomas Leanderson
President and CEO
Tel: +46 (0)46 19 20 95
Hans Kolam
CFO
Tel: +46 (0)46 19 20 44
Active Biotech AB
(Corp Reg. No. 556223-9227)
PO Box 724, SE-220 07 Lund
Tel: +46 (0)46 19 20 00
Fax: +46 (0)46 19 11 00