Likelihood of Approval and Phase Transition Success Rate Model – Ustekinumab Biosimilar in Psoriatic Arthritis
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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.


Ustekinumab Biosimilar in Psoriatic Arthritis Drug Details:
Ustekinumab (Yesintek) is a human monoclonal antibody used as immunosuppressant. It is formulated as solution for intravenous route of administration and as prefilled solution for subcutaneous route of administration. Yesintek is indicated for the treatment of Crohn’s disease (regional enteritis), plaque psoriasis (psoriasis vulgaris), psoriatic arthritis and ulcerative colitis.Ustekinumab biosimilar (Bmab 1200) is under development for the treatment of Crohn’s disease, plaque psoriasis, ulcerative colitis and psoriatic arthritis. The drug candidate is monoclonal antibody that acts by targeting interleukin 12 subunit beta and interleukin 23 subunit alpha. The drug candidate is administered through subcutaneous route.
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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