Cell & Gene Therapies in CNS Disorders - Update
Summary
Currently, there are nine cell and gene therapies (CGTs) on the market for various central nervous system (CNS) disorders. This includes three gene therapies, three gene-modified cell therapies, and three conditionally approved cell therapies. Novartis’s Zolgensma (onasemnogene abeparvovec) for the treatment of spinal muscular atrophy (SMA) was the first CGT asset to receive traditional approval in the CNS market in 2019. Over the past five years, there has been an increase in the number of traditionally approved CGTs for genetic disorders such as metachromatic leukodystrophy (MLD), cerebral adrenoleukodystrophy (CALD), aromatic L-amino acid decarboxylase deficiency (AADCD), and Duchenne muscular dystrophy (DMD).
GlobalData anticipates that the global CGT market value in CNS disorders will experience significant growth-sales are expected to increase from $2.3 billion in 2024 to $12.6 billion in 2030, at a compound annual growth rate (CAGR) of 32.8%. Gene therapies will dominate the CGT market in CNS disorders. This is attributed to strong players such as Sarepta Therapeutics and Novartis with their marketed products Elevidys and Zolgensma, respectively.
Scope
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