Melatonin is under clinical development by RepoCeuticals and currently in Phase II for Anorectal Disease. According to GlobalData, Phase II drugs for Anorectal Disease does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the Melatonin LoA Report. Buy the report here.
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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.
Melatonin overview
Melatonin is under development for the treatment of radiodermatitis, radiation cystitis, radiation proctitis, radiation vaginitis, low anterior resection syndrome and actinic (solar) keratosis. It is administered through intravenous, rectal, intravesical, vaginal, oral, inhalational, transdermal, cutaneous routes. It is a repurposed drug candidate. It was under development for the treatment of radiation pneumonitis.
For a complete picture of Melatonin’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.
