ML-007 is under clinical development by MapLight therapeutics and currently in Phase I for Alzheimer’s Disease. According to GlobalData, Phase I drugs for Alzheimer’s Disease have a 63% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how ML-007’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
ML-007 overview
ML-007 is under development for the treatment of Alzheimer’s disease psychosis and schizophrenia. The therapeutic candidate is a combination product targets muscarinic acetylcholine receptor M1 and muscarinic acetylcholine receptor M4. The drug candidate is being developed based on optogenetics and STARmap (three-dimensional spatial transcriptomics) platform. It is administered through oral route.
It was also under development for the treatment of dyskinesia.
MapLight therapeutics overview
MapLight therapeutics. (formerly Alvarado Therapeutics, Inc.), is a biopharmaceutical company focusing on drug discovery for diseases of the central nervous system. The company is headquartered in United States.
For a complete picture of ML-007’s drug-specific PTSR and LoA scores, buy the report here.
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