Detomidine is under clinical development by Clexio Biosciences and currently in Phase II for Pruritus. According to GlobalData, Phase II drugs for Pruritus have a 50% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Detomidine’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.

Detomidine overview

Detomidine (CLE-400) is under development for the treatment of post-operative pain, peripheral neuropathic pain, chronic pruritus. It is administered by topical route and formulated in the form of gel. The drug candidate acts by targeting the alpha2 adrenergic receptor. It was also under development for the treatment of painful diabetic neuropathy.

Clexio Biosciences overview

Clexio Biosciences (Clexio) is a clinical-stage pharmaceutical company focused on the development of novel drugs, small molecules, and drug-device combinations for the treatment pain, depression and other central nervous system (CNS) indications. Its pipeline product portfolio includes CLE-100, an oral NMDA receptor modulator for adjunctive therapy in major depressive disorder; CLE-300, a disruptive platform of wearable drugs; CLE-400, a topical formulation for the treatment of PDN and CLE-500, a patient-controlled drug-device combination for immediate relief of cluster headaches. The company also developed a proprietary oral gastro-retentive drug delivery platform (CLE-600) used for both extending the absorption window and controlled release of multiple pill burdens of numerous drugs. Clexio is headquartered in Jerusalem, Israel.

For a complete picture of Detomidine’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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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.