Likelihood of Approval and Phase Transition Success Rate Model – Immune Globulin (Human) in Chronic Lymphocytic Leukemia (CLL)
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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.


Immune Globulin (Human) in Chronic Lymphocytic Leukemia (CLL) Drug Details:
Human immunoglobulin (Privigen / Hizentra / Beriglobin / Beriglobina P / Beriglobin P / Sandoglobuline / Vivaglobin / Intragam / Privigen AU / Hizentra AU / Evogam / Carimune NF / Sandoglobulin / Behrigamma / Sandoglobulin NF / Armoglobulina P / Gama Venina / Venimmuna N ) is a liquid formulation of human immunoglobulin (Ig). It is formulated as Privigen injectable solution for intravenous administration, Carimune NF lyophilized powder for solution for intravenous administration and as Hizentra injectable solution for subcutaneous administration. Hizentra is indicated for the treatment of primary immunodeficiency (PI). Privigen is used for treatment of primary humoral immunodeficiency and chronic immune thrombocytopenic purpura Privigen is purified from the pooled plasma of thousands of healthy donors, so it contains a wide variety of the antibody specificities and idiotypes available in the general human population. It is also indicated for the treatment of Hypogammaglobulinaemia. This allows Privigen to be used for the treatment of immune disorders requiring immunoglobulin replacement. It acts by suppling opsonic and neutralizing IgG antibodies against bacterial, viral, parasitic and mycoplasma agents and their toxins. Privigen is also indicated for the treatment of adults with chronic inflammatory demyelinating polyneuropathy (CIDP) to improve neuromuscular disability, and for the treatment of hypogammaglobulinemia and agammaglobulinemia.The drug candidate is under development for the treatment of post-COVID postural orthostatic tachycardia syndrome, primary immune deficiency, diffuse cutaneous systemic sclerosis (subcutaneous formulation), idiopathic inflammatory myopathies and primary immunodeficiency syndromes with impaired antibody production and secondary immunodeficiencies in patients who suffer from severe or recurrent infections, ineffective antimicrobial treatment and either proven specific antibody failure (PSAF) or serum IgG level of less than 4 g/l and chronic lymphocytic leukemia (CLL). It was also under development for the treatment of Guillain-Barre syndrome and diffuse cutaneous systemic sclerosis (intravenous formulation), autoimmune epilepsy, dermatomyositis, acute traumatic spinal cord injury and immune-mediated necrotizing myopathy.
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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