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New Technologies Initiative: Gateway to Treating Genetic Diseases - Sarepta Therapeutics - Skipping Makes Sense - Restoring Muscle Function in Duchenne Muscular Dystrophy

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Approval of KYNAMRO (ISIS/Sanofi, HoFH), a first systemic Oligonucleotide Antisense (ASO) based therapy has raised expectations from the compounds in pipeline of other companies with similar technology platforms. Highly differentiated, 2nd Generation DNA/RNA-based drugs that work at the fundamental level of gene and protein expression have the potential to bring a paradigm change in treating diseases esp. rare genetic disorders like Familial Hypercholesterolemia (FH), Duchenne Muscular Dystrophy (DMD), TTR (Transthyretin amyloidosis), SMN (spinal muscular atrophy) etc. Noteworthy, amongst them besides ISIS Pharma (ISIS) are Sarepta Therapeutics (SRPT), Prosensa (Pvt.), Regulus (RGLS), Alnylam (ALNY), Idera (IDRA), Santaris (Pvt.), Acuity pharma (merged with Froptix corp.), Arrowhead Research Corporation (ARWR), etc. SRPTs lead compound Eteplirsen (formerly AVI-4658, PhII, based on proprietary exon-skipping technology, exon 51) targets specific mutations in DMD, repairs the mRNA and restores production of functional dystrophin protein = improved muscle functions. Duchenne Muscular Dystrophy (DMD) is a genetic (X-linked recessive) degenerative disease and Becker muscular dystrophy (BMD) is a milder form of DMD where the onset of the disease and disability is delayed.

In this report, we highlight the potential of the SRPTs Phosphorodiamidate Morpholino Oligomer (PMO) and Exon-Skipping technology platform. Key Points described in the report, are:
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Reports Details

Published Date : Mar 2013
No. of Pages :18
Country :Global
Category :Healthcare
Publisher :MP Advisors
Report Delivery By :Email
Report Delivery Time :12 to 24 hours after placing the order.

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