Plozasiran sodium is under clinical development by Arrowhead Pharmaceuticals and currently in Pre-Registration for Familial Chylomicronemia (Type I Hyperlipoproteinemia). According to GlobalData, Pre-Registration drugs for Familial Chylomicronemia (Type I Hyperlipoproteinemia) does not have sufficient historical data to build an indication benchmark PTSR for Pre-Registration. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Plozasiran sodium LoA Report. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Plozasiran sodium overview
Arrowhead Pharmaceuticals overview
Arrowhead Pharmaceuticals (Arrowhead) is a biotech company that develops and commercializes gene silencing therapeutics. The company utilizes RNA chemistries and TRiM platform to target and silence disease-causing genes. Its pipeline products include ARO-APOC3, ARO-ANG3, Olpasiran, GSK-4532990, ARO-PNPLA3, ARO-RAGE, ARO-MMP7, ARO-MUC5AC, Fazirsiran, ARO-HB, ARO-DUX4 and ARO-DM1. Arrowhead product indications include hypertriglyceridemia, dyslipidemia, cardiovascular disease, nonalcoholic steatohepatitis, inflammatory, idiopathic pulmonary fibrosis, idiopathic pulmonary fibrosis, much-obstructive, alpha-1 liver disease, hepatitis b, facioscapulohumeral muscular dystrophy and myotonic dystrophy type 1. The company operates lab facilities in San Diego, California and Madison, Wisconsin, the US. Arrowhead is headquartered in Pasadena, California, the US.
For a complete picture of Plozasiran sodium’s drug-specific PTSR and LoA scores, buy the report here.
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