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Meda Acquires Actinic Keratosis New Treatment European Rights

Meda has acquired exclusive European rights to a new formulation of imiquimod from Graceway Pharmaceuticals. The new formulation is 3,75% imiquimod topical cream indicated for the treatment of actinic keratosis (AK). The product has recently been approved in the US and Canada.

Meda said that it markets a higher strength (5%) of imiquimod in Europe under the trademark Aldara. In 2009, sales of Aldara were approximately 500 MSEK.

3,75% imiquimod can be used on a larger treatment area, it is once-daily and more tolerable due to the decreased concentration. The patent for this novel imiquimod formulation is pending.

Graceway Pharma is continuing its development program around 3,75% imiquimod. Meda has exclusive rights to follow-up products based on the imiquimod substance.

In consideration for exclusive European rights for 3,75% imiquimod, Meda is expected to pay Graceway Pharma an undisclosed up-front and a single digit royalty on net sales. No milestones payments will be due for 3,75% imiquimod.

Anders Lonner, CEO at Meda, said: “We have very good experience with Aldara in Europe and we look forward to provide AK patients with a new product with improved tolerability that builds on the efficacy of imiquimod.”