Likelihood of Approval and Phase Transition Success Rate Model – Solriamfetol Hydrochloride in Shift Work Sleep Disorder
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This report provides you with the data that allows you to track and predict the specific likelihood of approval (LOA) and phase transition success rate (PTSR) of a drug using GlobalData’s proprietary machine learning algorithms developed using over 10 years of historical data.


Solriamfetol Hydrochloride in Shift Work Sleep Disorder Drug Details:
Solriamfetol hydrochloride (Sunosi) was a phenylalanine derivative, acts as an wake-promoting agent. It is formulated as film coated tablets for oral route of administration. Sunosi is indicated to improve wakefulness in adult patients with excessive daytime sleepiness associated with narcolepsy or obstructive sleep apnea (OSA), and to improve wakefulness and reduce excessive daytime sleepiness (EDS) in adult patients with obstructive sleep apnoea (OSA) whose EDS has not been satisfactorily treated by primary OSA therapy, such as continuous positive airway pressure (CPAP).Solriamfetol hydrochloride (SKL-N05/JZP-110/ADX-N05) is under development for the treatment of attention deficit hyperactivity disorder (ADHD), excessive sleep in idiopathic Parkinson’s disease, obstructive sleep apnea, binge eating disorder (BED), major depressive disorder, shift work disorder, fatigue. The drug candidate is an optically pure phenylalanine derivative. It is administered orally. The adrenergic agent was also under development for the treatment of drug addiction and major depressive disorder, pediatric subjects with narcolepsy.
Report Coverage
The data is segmented by drug name per indication and shows the current likelihood of approval for the drug compared to the indication benchmark and the industry benchmark.
The Likelihood of Approval data is updated regularly based on events that take place which impact the clinical development process and regulatory considerations. GlobalData’s proprietary machine learning models consider these events in real time, to produce quantitative changes to the LOA and PTSR along with qualitative reasoning why the likelihood of approval has changed.
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Reasons to Buy
- Precise Likelihood of Approval and Phase Transition Success Rates: Our machine learning and proprietary models provide accurate predictions, helping you gauge the potential success of a drug in the regulatory process.
- Competitive Strategy Planning: Access information on LOA and PTSR for competitors’ drugs, allowing you to plan your clinical development, commercialisation and marketing strategies
- Event-driven Updates: Track event-driven changes in LOA and PTSR benchmarked against indication LOA/PTSR. Get the latest insights to adapt your strategies promptly!
- Well-informed Investment Decisions: This data helps you navigate the dynamic landscape of drug development and regulatory considerations.
Scope
- Drug Details: Drug name, Drug type, Intervention type
- Administration Pathway
- Therapeutic Areas
- Key Manufacturers
- Drug Development Status
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