Montelukast sodium is under clinical development by Jiangyin Berrysen Pharmaceutical and currently in Phase II for Cervical Cancer. According to GlobalData, Phase II drugs for Cervical Cancer have a 35% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Montelukast sodium’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.
Montelukast sodium overview
Montelukast sodium is under development for the treatment of radiation injury, pelvic malignancy including cervical cancer, endometrial cancer. It is administered through rectal route as gel and acts by targeting CysLT1 receptor.
It was also under development for the treatment of hemorrhoids.
Jiangyin Berrysen Pharmaceutical overview
Jiangyin Berrysen Pharmaceutical (Berrysen Pharma) operates in healthcare sector. Berrysen Pharma is headquartered in Jiangyin, China.
For a complete picture of Montelukast sodium’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.
