BAER-101 is under clinical development by Baergic Bio and currently in Phase II for Anxiety Disorders. According to GlobalData, Phase II drugs for Anxiety Disorders have a 35% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how BAER-101’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.

BAER-101 overview

BAER-101 is under development for the treatment of anxiety disorders, depression, refractory epilepsy, dravet syndrome (Severe Myoclonic Epilepsy of Infancy) and fragile X syndrome. BAER-101 (AZD-7325) is a new chemical entity that is administered orally. AZD-7325 acts by targeting gamma-aminobutyric acid (GABA) receptor subunit alpha 2,3.

For a complete picture of BAER-101’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 2 September 2023

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.