HS-135 is under clinical development by 35Pharma and currently in Phase I for Diastolic Heart Failure (HFpEF). According to GlobalData, Phase I drugs for Diastolic Heart Failure (HFpEF) 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 HS-135 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.
HS-135 overview
HS-135 is under development for the treatment of pulmonary hypertension and obesity-associated heart failure with preserved ejection fraction. The therapeutic candidate is a biologic which is administered through sub-cutaneous route. It acts by targeting activin and GDF.
35Pharma overview
35Pharma is a biopharmaceutical company that designs and develops biologics for pulmonary hypertension and musculoskeletal disorders. 35Pharma is headquartered in Montreal, Quebec, Canada.
For a complete picture of HS-135’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.
