Theophylline is under clinical development by Cyrano Therapeutics and currently in Phase II for Hyposmia. According to GlobalData, Phase II drugs for Hyposmia 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 Theophylline 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.
Theophylline overview
Theophylline is under development for the treatment of hyposmia and dysgeusia (taste disorders).The drug candidate is administered through intranasal route as a spray and solution form. It acts by targeting phosphodiesterase.
Cyrano Therapeutics overview
Cyrano Therapeutics is a clinical stage regenerative medicine company. The company develops therapy for people struggling with the loss of smell and flavor. It creates a special, exclusive intranasal medication to help patients with chronic loss of taste and smell regain function. Its major product under development is CYR-064, which is being tested in a randomized, double-blinded, placebo-controlled trial. The company’s services are primarily aimed at patients suffering from smell loss due to various causes, including sinonasal disease, viral upper respiratory infection, and head trauma. Cyrano Therapeutics is also addressing the significant increase in smell and flavor loss due to the COVID-19 pandemic. It operates in North America and Europe. Cyrano Therapeutics is headquartered in Delray Beach, Florida, the US.
For a complete picture of Theophylline’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.
