TMP-301 is under clinical development by Tempero Bio and currently in Phase I for Amyotrophic Lateral Sclerosis. According to GlobalData, Phase I drugs for Amyotrophic Lateral Sclerosis have an 87% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how TMP-301’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.
TMP-301 overview
TMP-301 (HTL-14242) is under development for the treatment of dystonia, Parkinson's disease, amyotrophic lateral sclerosis, substance use disorders, alcohol use disorders, cocaine use disorder and anxiety. The drug candidate act by targeting metabotropic glutamate receptor 5 (mGluR5). It is administered through oral route. It is developed based on StaR technology and GPCR structure-based drug design (SBDD) platform. It was under development for depression, dyskinesia in Parkinson's disease, autism and other neurological diseases.
Tempero Bio overview
Tempero Bio is a drug development company. Tempero Bio is headquartered in Delaware, the US.
For a complete picture of TMP-301’s drug-specific PTSR and LoA scores, buy the report here.
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