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