Fentanyl is under clinical development by MEDRx and currently in Phase I for Pain. According to GlobalData, Phase I drugs for Pain have a 75% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Fentanyl’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.
Fentanyl overview
Fentanyl (MRX-9FLT) is under development for the treatment of moderate to severe pain. It is administered through transdermal route as patch. It acts by targeting opioid (Mu) receptor. The drug candidate is developed based on transdermal formulation technology using nano-sized colloid transdermal system (NCTS).
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MEDRx overview
MEDRx through its subsidiaries carries out development of pharmaceutical drug based on the transdermal absorption system. The company focuses on ionic liquid technology to develop ionic liquid transdermal system (ILTS) and transdermal medicines that include ETOREAT, MRX-10XT, MRX-5LBT, MRX-4TZT and MRX-5DML. The company also develops anti-Alzheimer’s drugs, local analgesics and antidepressants. MEDRx also offers microneedle array “Patch Vaccine” for providing vaccines. It partners with many pharmaceutical companies for development of various drugs. The company operates across the US and Japan. MEDRx is headquartered in Higashikagawa City, Japan.
For a complete picture of Fentanyl’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.
