Vaxil Bio's ImMucin receives EMA orphan drug designation for treatment of Multiple Myeloma

Vaxil Bio (TASE: VAXL), a leading developer of immunotherapeutic products to treat cancer and infectious diseases, reports today that its lead drug candidate, ImMucin has received orphan drug designation from the European Medicines Agency (EMA) of the European Commission (EC) for the treatment of Multiple Myeloma (MM), a blood cancer. ImMucin targets the less studied Signal Peptide domain of the MUC1 tumor antigen, which harbors key advantages as an anti-MM modality.

Orphan designation by the EMA is granted to promote the clinical development of drugs that target rare life-threatening or debilitating conditions and which are expected to provide significant therapeutic advantage over existing treatments. Orphan designation provides significant benefits, including ten years of market exclusivity following marketing approval, reductions in the fees and costs of the regulatory process and scientific assistance from the EMA in clinical development.

Dr. Lior Carmon, Vaxil's Founder and CEO comments: "Obtaining orphan drug designation for ImMucin in the European Union is a highly important milestone in the development of this novel treatment. There are still limited treatment options for those MM patients with "minimal residual disease" i.e. in a state where the disease is in remission or near remising but with residual tumor cells in the bone marrow, which are known today to lead to inferior overall survival. These patients are looking for a maintenance treatment that can manage their disease and stop or at least delay relapse. We are excited about ImMucin's prospects to potentially treat these patients as validated by the EMA's decision. This will obviously be further evaluated in our upcoming clinical trial due to start this year."


Vaxil Bio


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