Patidistrogene bexoparvovec is a Gene Therapy owned by Sarepta Therapeutics, and is involved in 2 clinical trials, which were completed.
patidistrogene bexoparvovec (SRP-9004) comprises self-complementary recombinant adeno-associated virus serotype rhesus 74 (AAVrh.74) encoding alpha-sarcoglycan. Limb-girdle muscular dystrophy type 2D (LGMD2D) occurs due to mutations in alpha-sarcoglycan (ASG) gene leading to muscle weakness. Sarcoglycan alpha is a dystrophin-associated glycoprotein gene which encodes a component of the dystrophin-glycoprotein complex (DGC). It induces stabilization of muscle fiber membranes and linking of the actin cytoskeleton to the extracellular matrix. The drug candidate by delivering the functional copy of alpha-sarcoglycan promotes the encoding of functional protein and ameliorates the disease condition.
The revenue for Patidistrogene bexoparvovec is expected to reach a total of $458m through 2038. This change impacts the valuation of this asset and is an important factor to understand the current value of the drug in a clinical process. View the complete picture with the Patidistrogene bexoparvovec NPV Report.
Patidistrogene bexoparvovec was originated by Nationwide Children’s Hospital and is currently owned by Sarepta Therapeutics.
Patidistrogene bexoparvovec Overview
patidistrogene bexoparvovec (SRP-9004) is under development for the treatment of limb-girdle muscular dystrophy type 2D (LGMD2D). It is administered through injection. The therapeutic candidate comprises self-complementary recombinant adeno-associated virus serotype rhesus 74 (AAVrh.74) encoding alpha-sarcoglycan.
Sarepta Therapeutics Overview
Sarepta Therapeutics (Sarepta) discovers and develops unique RNA-targeted medicines to treat rare diseases. The company develops its pipeline products using its multi-platform Precision Genetic Medicine Engine in gene therapy, RNA, and gene editing. The company’s platform is based on its pioneering work with phosphorodiamidate morpholino oligomer (PMO) chemistries. Its commercial products include Exondys 51, Vyondys 53 and Amondys 45 indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients who have a confirmed mutation of the DMD gene. Its pipeline product includes SRP-5051, SRP-9001, SRP-9003 and SRP-5045 indicated for the treatment of DMD, limb-girdle muscular dystrophies (LGDMs) and other neuromuscular and central nervous system disorders. Sarepta is headquartered in Cambridge, Massachusetts, the US.
The company reported revenues of (US Dollars) US$701.9 million for the fiscal year ended December 2021 (FY2021), an increase of 30% over FY2020. The operating loss of the company was US$362.2 million in FY2021, compared to an operating loss of US$456.1 million in FY2020. The net loss of the company was US$418.8 million in FY2021, compared to a net loss of US$554.1 million in FY2020.
The company reported revenues of US$230.3 million for the third quarter ended September 2022, a decrease of 1.4% over the previous quarter.
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