ReS-19T is under clinical development by ReMYND 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 ReS-19T’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.
ReS-19T overview
ReMYND overview
reMYND is a clinical-stage company that develops disease-modifying treatments caused by cellular dysfunction. The company’s pipeline programs include ReS19-T, ReS9-S ReS3-T and ReS18-H. Its pipeline candidates treat alzheimer’s, epilepsy, parkinson’s and huntington’s disease. reMYND also provides contract research services to its clients to assess the pharmacokinetics, pharmacodynamics and efficacy of experimental treatments in its proprietary animal models. The company’s CRO technology platform concentrates on protein-misfolding disorders such as Huntington’s disease and amyotrophic lateral sclerosis to discover and develop drug candidates. reMYND is headquartered in Leuven, Brabant Flamand, Belgium.
For a complete picture of ReS-19T’s drug-specific PTSR and LoA scores, buy the report here.
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