Breakthrough
Sanofi and subsidiary Genzyme have announced that the FDA has granted breakthrough therapy designation to olipudase alfa, an enzyme replacement therapy being investigated for the treatment of patients with non-neurological manifestations of acid sphingomyelinase deficiency (ASMD), also known as Niemann-Pick disease Type B.
ASMD is a serious and life-threatening disorder caused by insufficient activity of the enzyme acid sphingomyelinase (ASM), which results in toxic accumulation of sphingomyelin. There are currently no approved treatment options for patients with Niemann-Pick Type B.
Breakthrough therapy designation is intended to expedite the development and review of investigational new drugs that target serious or life-threatening conditions. The criteria for granting Breakthrough Therapy designation are preliminary clinical evidence of substantial improvement on a clinically significant endpoint over available therapies. The breakthrough therapy designation is distinct from the FDA's other mechanisms to expedite drug development and review, and will allow for a close collaboration between Genzyme and the FDA on the olipudase alfa development programme.
Olipudase alfa is being developed by Genzyme to potentially address the fundamental defect underlying the disease. Supplementing the defective or deficient native enzyme with olipudase alfa allows for the breakdown of sphingomyelin, whose accumulation is responsible for the clinical manifestation of ASMD.
The Breakthrough Therapy designation is supported by data from a completed Phase 1b study of olipudase alfa. Findings in five adult patients with nonneuronopathic ASMD were presented at the Lysosomal Disease Network's WORLD Symposium in February 2015. The data presented on the repeat-dose safety, pharmacodynamics and exploratory efficacy of olipudase alfa support its continued development for the investigational use in non-neurological manifestations of ASMD.
"There is tremendous unmet need in the ASMD/Niemann-Pick Type B community, and we are hopeful that olipudase alfa can be developed into a meaningful treatment for patients," said Genzyme's Global Head of Rare Diseases, Richard Peters, MD, Ph.D. "We appreciate FDA's support for this important programme, giving us the opportunity to utilise an important expedited drug development pathway for olipudase alfa and providing hope for patients affected with a chronic and progressively debilitating disease."
The company has started enrolment of a Phase 1/2 paediatric study and is preparing for enrolment of a Phase 2/3 adult study in the second half of 2015. For more information, please visit http://clinicaltrials.gov.