Drug Summary
INBRIJA consists of a dry powder formulation of levodopa for oral inhalation with the INBRIJA inhaler. The inhalation powder is packaged in white hypromellose capsules. Each capsule contains a spray-dried powder of 42 mg levodopa active ingredient with 1, 2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) and sodium chloride.The active component of INBRIJA is levodopa, an aromatic amino acid. Its chemical name is (2S)-2-amino-3-(3,4-dihydroxyphenyl) propanoic acid and its molecular weight is 197.19 g/mol and the molecular formula is C9H11NO4.
Dosage and Administration
INBRIJA consists of a dry powder formulation of levodopa for oral inhalation with the INBRIJA inhaler. The therapeutic capsule contains 42 mg levodopa for use in an INBRIJA inhaler. The INBRIJA inhaler is a plastic device with a blue body, blue cap, and white mouthpiece used for inhaling INBRIJA powder. INBRIJA capsules are needed up to 5 times daily. The maximum recommended daily dosage of INBRIJA is 420 mg.Mechanism of Action
Levodopa, the metabolic precursor of dopamine, crosses the blood-brain barrier and presumably is converted to dopamine in the brain. This is thought to be the mechanism whereby levodopa relieves symptoms of Parkinson's disease.Scope of the Report
The report provides insights into:- A comprehensive product overview including the INBRIJA description, mechanism of action, dosage and administration, research and development activities in Parkinson's disease.
- Elaborated details on INBRIJA regulatory milestones and other development activities have been provided in this report.
- The report also highlights the INBRIJA research and development activities in Parkinson's disease across the United States, Europe and Japan.
- The report also covers the patents information with expiry timeline around INBRIJA.
- The report contains forecasted sales of INBRIJA for Parkinson's disease till 2032.
- Comprehensive coverage of the late-stage emerging therapies for Parkinson's disease.
- The report also features the SWOT analysis with analyst views for INBRIJA in Parkinson's disease.
Methodology
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis a team of industry experts. Information and data from the secondary sources have been obtained from various printable and nonprintable sources like search engines, news websites, global regulatory authorities websites, trade journals, white papers, magazines, books, trade associations, industry associations, industry portals and access to available databases.INBRIJA Analytical Perspective
In-depth INBRIJA Market Assessment
This report provides a detailed market assessment of INBRIJA for Parkinson's disease in the seven major markets, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan. This segment of the report provides forecasted sales data from 2024 to 2032.INBRIJA Clinical Assessment
The report provides the clinical trials information of INBRIJA for Parkinson's disease covering trial interventions, trial conditions, trial status, start and completion dates.Report Highlights
- In the coming years, the market scenario for Parkinson's disease is set to change due to the extensive research and incremental healthcare spending across the world; which would expand the size of the market to enable the drug manufacturers to penetrate more into the market.
- The companies are developing therapies that focus on novel approaches to treat/improve the disease condition, assess challenges, and seek opportunities that could influence INBRIJA dominance.
- Other emerging products for Parkinson's disease are expected to give tough market competition to INBRIJA and launch of late-stage emerging therapies in the near future will significantly impact the market.
- A detailed description of regulatory milestones, and developmental activities, provide the current development scenario of INBRIJA in Parkinson's disease.
- This in-depth analysis of the forecasted sales data of INBRIJA from 2024 to 2032 will support the clients in the decision-making process regarding their therapeutic portfolio by identifying the overall scenario of the INBRIJA in Parkinson's disease.
Key Questions Answered
- What is the product type, route of administration and mechanism of action of INBRIJA?
- What is the clinical trial status of the study related to INBRIJA in Parkinson's disease and study completion date?
- What are the key collaborations, mergers and acquisitions, licensing and other activities related to the INBRIJA development?
- What are the key designations that have been granted to INBRIJA for Parkinson's disease?
- What is the forecasted market scenario of INBRIJA for Parkinson's disease?
- What are the forecasted sales of INBRIJA in the seven major countries, including the United States, Europe (Germany, France, Italy, Spain, and the United Kingdom), and Japan?
- What are the other emerging products available and how are these giving competition to INBRIJA for Parkinson's disease?
- Which are the late-stage emerging therapies under development for the treatment of Parkinson's disease?
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