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ÇÏÀÌÁ¨Æ®¶ó ½Å±Ô ¾àÁ¦ ÀλçÀÌÆ®¿Í ½ÃÀå ¿¹Ãø(2032³â)HIZENTRA Emerging Drug Insight and Market Forecast - 2032 |
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ÇöÀç ¼ºÀÎ DM ȯÀÚ¸¦ ´ë»óÀ¸·Î ÇÑ ÀÓ»ó 3»ó(RECLAIIM)ÀÌ ÁøÇà ÁßÀ̸ç, 2027³â 11¿ù±îÁö ¿Ï·áµÉ ¿¹Á¤ÀÔ´Ï´Ù.
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“"HIZENTRA Emerging Drug Insight and Market Forecast - 2032" ” report provides comprehensive insights about HIZENTRA for dermatomyositis in the seven major markets. A detailed picture of the HIZENTRA for dermatomyositis in the 7MM, i.e., the United States, EU4 (Germany, France, Italy, and Spain) and the United Kingdom, and Japan for the study period 2019 -2032 is provided in this report along with a detailed description of the HIZENTRA for dermatomyositis. The report provides insights about mechanism of action, dosage and administration, as well as research and development including regulatory milestones, along with other developmental activities. Further, it also consists of future market assessments inclusive of the HIZENTRA market forecast analysis for dermatomyositis in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in dermatomyositis.
HIZENTRA is a sterile, clear, colorless, pale-yellow, light-brown solution of normal human immunoglobulin for SC injection. It is a 20% solution containing 20 g/100 mL of total human plasma protein with a purity of at least 98% immunoglobulin G (IgG). More than 90% of the IgG consists of monomers and, dimers, aggregates (≤2%, typically below 0.1%). The distribution of the IgG subclasses is similar to that of normal human plasma (approximate values: 69% IgG1, 26% IgG2, 3% IgG3, 2% IgG4). The product contains 250 mmol/L of proline as a stabilizer, a physiological nonessential amino acid; the product also contains trace amounts of polysorbate 80 and sodium. HIZENTRA contains no carbohydrate stabilizer (e.g., sucrose, maltose) and no preservative.
Currently, the molecule is under investigation in a Phase III (RECLAIIM) clinical trial for adult patients with DM, anticipated to be completed by November 2027.
The report provides insights into:
The report is built using data and information sourced primarily from internal databases, primary and secondary research and in-house analysis by DelveInsight's 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.
This report provides a detailed market assessment of HIZENTRA for dermatomyositis 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 2025 to 2032.
The report provides the clinical trials information of HIZENTRA for dermatomyositis covering trial interventions, trial conditions, trial status, start and completion dates.