The European Commission Grants Orphan Drug Designation for Molmed's Vascular Targeting Agent Arenegyr in the Treatment of Mesothelioma
The European Commission, which is the executive branch of the European Union, has granted “Orphan Drug” status to Arenegyr, an anti-cancer drug currently under investigation for the treatment of mesothelioma, as well as a number of other cancers. Arenegyr is an experimental vascular targeting agent that targets newly-formed tumor blood vessels and disrupts the vascular processes that feed the tumor. At low doses, the agent exhibits its own anti-tumor activity, but it also enhances the efficacy of other anti-cancer drugs used in combination with it. At high doses, it disrupts the vessels and can induce large-scale tumor breakdown and death.
Orphan Drug status is a designation given to therapies designed for uncommon conditions. The EU’s orphan drug status designation is restricted to conditions that occur in less than 5 in 10,000 people. The designation provides a number of benefits to companies developing the therapy and is a given after a therapy has shown some initial successes in clinical trials.
Arenegyr is produced by the Italian pharmaceutical company MolMed S.p.A. and is currently the subject of a number of clinical studies, both as a single-agent therapy and as a combination with therapy. These studies are investigating its use for pleural mesothelioma, colorectal cancer, hepatocarcinoma and small-cell lung carcinoma.
Labels: mesothelioma






