Likelihood of Approval and Phase Transition Success Rate Model – Sarilumab in Systemic-Onset Juvenile Idiopathic Arthritis (Still Disease)
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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.


Sarilumab in Systemic-Onset Juvenile Idiopathic Arthritis (Still Disease) Drug Details:
Sarilumab (Kevzara, REGN-88, SAR153191) is a monoclonal antibody developed by using velocImmune antibody technology. Kevzara is formulated as injectable solution for subcutaneous route of administration. Kevzara is indicated for treatment of adult patients with moderately to severely active rheumatoid arthritis (RA) who have had an inadequate response or intolerance to one or more disease-modifying antirheumatic drugs (DMARDs).Sarilumab is under development for the treatment of systemic juvenile idiopathic arthritis, polymyalgia rheumatica, polyarticular juvenile idiopathic arthritis (pjia), morphea (localized scleroderma). It was also under development for ankylosing spondylitis, giant cell arteritis, posterior uveitis, intermediate uveitis, non-infectious uveitis, pan-uveitis (NIU), and symptoms of Covid-19 and pneumonia.
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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