Navocaftor is under clinical development by Sionna Therapeutics and currently in Phase II for Cystic Fibrosis. According to GlobalData, Phase II drugs for Cystic Fibrosis have a 31% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Navocaftor’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.
Navocaftor overview
GLPG-3067 is under development for the treatment of cystic fibrosis. It is a small molecule administered through orally as a suspension. It targets the cystic fibrosis transmembrane conductance regulator (CFTR).
Sionna Therapeutics overview
Sionna Therapeutics is developing novel small molecule therapeutics for the treatment of cystic fibrosis. The company is headquartered in Waltham, Massachusetts, the US.
For a complete picture of Navocaftor’s drug-specific PTSR and LoA scores, buy the report here.
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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.
