BAER-101 is under clinical development by Baergic Bio and currently in the Phase II in clinical pathway. The characteristics of the clinical trial as well as other attributes related to the drug, regulations, and company play a fundamental role in ensuring the likelihood of transition that the drug moves from its current development stage to next.
According to GlobalData, the latest event to affect BAER-101’s likelihood of approval (LoA) and phase transition for Anxiety Disorders took place on 14 Nov 2022, which decreased the likelihood that the drug progresses to the next phase in its clinical pathway and decreased the likelihood of final approval for this indication.
GlobalData uses proprietary data and analytics to provide a complete picture of this assessment in their BAER-101 Likelihood of Approval (LoA) and Phase Transition Success Rate (PTSR) Report.
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.
Quick View BAER-101 LOA Data
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