Likelihood of Approval and Phase Transition Success Rate Model – Avicursen in Relapsing Remitting Multiple Sclerosis (RRMS)
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Empower your strategies with our Likelihood of Approval and Phase Transition Success Rate Model – Avicursen in Relapsing Remitting Multiple Sclerosis (RRMS) report and make more profitable business decisions.
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.


Avicursen in Relapsing Remitting Multiple Sclerosis (RRMS) Drug Details:
ATL-1102, (TV-1102, ISIS 107248) is under development for the treatment of relapsing-remitting multiple sclerosis, Duchenne muscular dystrophy, limb girdle muscular dystrophy R2, epilepsy and other inflammatory diseases. It is administered through subcutaneous, inhalation route of administration. It is formulated as a solution for multiple sclerosis. ATL1102 is a second-generation antisense inhibitor of CD49d, a subunit of VLA-4 (very late antigen-4). The therapeutic candidate is developed based on antisense technology. It was also under development for the treatment of asthma, acute myeloid leukemia and secondary progressive multiple sclerosis (SPMS).
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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