Gene silencing for CNS diseases
Two oligonucleotide drugs are to enter the clinic this year for the treatment of Huntington’s disease and epilepsy using a technology that directly targets the brain and spinal cord. The developer, Atalanta Therapeutics Inc of Boston, US, announced the prospective trials on 28 January alongside the close of a $97 million Series B financing round which will bring the candidate therapies up to the clinical proof-of-concept stage. The financing was co-led by the private equity group EQT Life Sciences and Sanofi Ventures.