GH-002 is under clinical development by GH Research and currently in Phase I for Unspecified Neurologic Disorders. According to GlobalData, Phase I drugs for Unspecified Neurologic Disorders does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the GH-002 LoA Report. 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.
GH-002 overview
GH-002 is under development for the treatment of treatment resistant depression and unspecified neurological disorders. The drug candidate is an injectable formulation of 5-methoxy-N,N-dimethyltryptamine (5-MeO-DMT). It acts by targeting serotonin 5HT1A and 5HT2A. It is administered through intravenous bolus route.
GH Research overview
GH Research biopharmaceutical company developing novel therapies for psychiatric and neurological disorders. The company has desigend its proprietary inhalable 5-MeO-DMT for depression. GH Research is headquartered in Dublin, Ireland.
For a complete picture of GH-002’s drug-specific PTSR and LoA scores, buy the report here.
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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.
