Received Marketing Authorization in France

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(Lysaker, Norway, 04 June 2007) Navamedic ASA has received the draft Marketing Authorization (MA) for Glucomed/Flexove in France.



Navamedic has received the MA in draft version, and has been given the chance to update the French text on the packaging, leaflets etc if and as required by the company. Following the submission of any such updates, the formal MA is expected shortly.




The company will start the process of applying for reimbursement for the product in France as soon as the formal MA is received.




In addition to the MA in France, Navamedic has received MA in Spain .



Launch of Glucomed/Flexove is expected to follow the timelines presented in the Q1-report.









For further information, please contact:



Øyvind W. Brekke, CEO Navamedic ASA
E-mail: oyvind.brekke@navamedic.com
Office: +47 67 11 25 40
Mobile: +47 91 19 81 64



Bernt-Olav Røttingsnes, CFO/IRO Navamedic ASA
E-mail: bor@navamedic.com
Office: +47 67 11 25 44
Mobile: +47 91 34 70 21






About Navamedic ASA:
Navamedic is a Norwegian speciality pharmaceutical company focusing on the development and production of glucosamine HCl (hydrochloride) based medicines. Glucosamine is a generic active ingredient which relieves pain and improves function in patients with mild to moderate osteoarthritis. The product has a favourable safety profile. Osteoarthritis is a chronic disease which affects a large and growing share of the world`s population. Navamedic aims to become a leading company in the glucosamine industry, with a competitive advantage in proprietary production technology. Navamedic`s product Glucomed/Flexove has been approved across 25 EU/EEA states by European Medicines Agency (EMEA), as the first and only glucosamine based medicine against osteoarthritis. The company`s products will be sold through a network of sales, marketing and distribution partners. For more information, please see www.navamedic.com

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