Likelihood of Approval and Phase Transition Success Rate Model – Imlifidase in Guillain-Barre Syndrome
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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.


Imlifidase in Guillain-Barre Syndrome Drug Details:
Imlifidase (Idefirix) is an immunosuppressive agent. It is formulated as powder for concentrate for solution for intravenous, parenteral route of administration. It is a unique IgG antibody-cleaving enzyme indicated for desensitisation treatment of highly sensitised adult kidney transplant patients with positive crossmatch against an available deceased donor. Imlifidase is under development for the treatment of antibody mediated rejection of HLA sensitized kidney after transplantation, acute autoimmune diseases including Guillian-Barre syndrome, anti-glomerular basement membrane (anti-GBM) disease (Goodpasture Syndrome), anti-neutrophil cytoplasmic antibodies (ANCA) associated vasculitis, granulomatosis with polyangiitis, neuromyelitis optica spectrum disorder, microscopic polyangiitis, acute respiratory distress syndrome and pulmonary alveolar hemorrhage. IdeS (Immunoglobulin G-degrading enzyme of Streptococcus pyogenes) is recombinantly produced immunoglobulin G-degrading enzyme of S.pyogenes.It was also under development for the treatment of asymptomatic antibody-mediated thrombotic thrombocytopenic purpura.
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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