AL-001 is under clinical development by Alzamend Neuro and currently in Phase II for Alzheimer’s Disease. According to GlobalData, Phase II drugs for Alzheimer’s Disease have a 36% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how AL-001’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks.
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.
AL-001 overview
Liprosal is under development for the treatment of bipolar disorder, major depressive disorder, post traumatic stress disorder (PTSD), dementia related to mild, moderate, and severe cognitive impairment associated with Alzheimer’s disease. The drug candidate is a cocrystal based therapy comprising of lithium salicylate and L-proline. It is administered orally. Lithium acts by targeting glycogen synthase kinase 3 alpha, beta (GSK3A, GSK3B) and inositol mono/polyphosphatase (IMPase, IPPase). L-proline reduces the hygroscopic property of salicylate salt. The drug candidate was also under development for fragile x syndrome.
Alzamend Neuro overview
Alzamend Neuro is a biotechnology company, based in the US. The company develops and commercializes drugs, treatments and cures for Alzheimer’s disease.
For a complete picture of AL-001’s drug-specific PTSR and LoA scores,
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