Acetylleucine is under clinical development by IntraBio and currently in Pre-Registration for Niemann-Pick Disease Type C. According to GlobalData, Pre-Registration drugs for Niemann-Pick Disease Type C 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 Acetylleucine 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.
Acetylleucine overview
Acetylleucine (IB-1001) is under development for the treatment of Niemann-Pick disease type C, GM1 Gangliosidosis, GM2 gangliosidosis, ataxia telangiectasia, spinocerebellar ataxia, Tay-Sachs Disease, multiple systems atrophy and Sandhoff disease. It is administered orally as powder for suspension.
It was under development for Lewy body dementia and frontotemporal dementia, Niemann-Pick disease type A and B and Alzheimer's Disease.
IntraBio overview
IntraBio is a private pharmaceutical company that focuses on the development and commercialization of novel and repurposed drugs to treat common and rare neurodegenerative diseases, including lysosomal storage disorders. The company is headquartered in Oxford, Oxfordshire, the UK.
For a complete picture of Acetylleucine’s drug-specific PTSR and LoA scores, buy the report here.
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