(Clenbuterol hydrochloride + nadolol) is under clinical development by CuraSen Therapeutics and currently in Phase II for Lewy Body Dementia. According to GlobalData, Phase II drugs for Lewy Body Dementia does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the (Clenbuterol hydrochloride + nadolol) 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.
(Clenbuterol hydrochloride + nadolol) overview
A fixed dose combination of clenbuterol hydrochloride (CST-103) and nadolol (CST-107) is under development for the treatment of lewy body dementia, mild cognitive impairment, and Parkinson's disease. It is administered through oral route. The drug candidate acts by targeting beta-2 adrenoceptor.
CuraSen Therapeutics overview
CuraSen Therapeutics is developing drugs targeting a novel mechanism in the brain to restore function, improve symptoms and modify disease in a range of neurodegenerative diseases, including orphan disorders as well as Parkinson’s Disease and Alzheimer’s Disease.
For a complete picture of (Clenbuterol hydrochloride + nadolol)’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
