Atavistik Bio has reeled in a $120 million Series B for its pipeline of small molecules to treat blood diseases. The Cambridge, MA, biotech is working on medicines for a severe bleeding disorder known as hereditary hemorrhagic telangiectasia and a group of rare, chronic blood cancers called myeloproliferative neoplasms. The new money will fund
those investigational drugs through clinical proof-of-concept, Atavistik said in its announcement Thursday. The program in hemorrhagic telangiectasia, an AKT1-selective inhibitor, will enter the clinic in the first half of 2026. Vaderis, Tectonic, Diagonal and other drug developers are also attempting to create medicines for the disease. Atavistik's work in myeloproliferative neoplasms is further behind in preclinical development. The company is
developing a JAK2 V617F mutant-selective inhibitor. |