Buspirone is under clinical development by Cingulate and currently in Phase I for Anxiety Disorders. According to GlobalData, Phase I drugs for Anxiety Disorders have a 68% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Buspirone’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.
Buspirone overview
Buspirone is under development for the treatment of anxiety disorders. It is administered through oral route in the form a tablet. The therapeutic candidate is an anxiolytic agent and is being developed based on precision timed release (PTR) drug delivery platform technology. It acts by targeting 5-hydroxytryptamine 1A (5-HT) and dopamine receptor 2 (D2).
Cingulate overview
Cingulate operates as a holding company. It develops drugs for the treatment of attention deficit/hyperactivity disorder (ADHD) and anxiety associated disorders through its subsidiary. The company is headquartered in Kansas City, Kansas, the US.
For a complete picture of Buspirone’s drug-specific PTSR and LoA scores, buy the report here.