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시장보고서
상품코드
1462271
TEPEZZA 시장 규모, 예측, 시장 인사이트(2032년)TEPEZZA Market Size, Forecast, and Market Insight - 2032 |
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인슐린 유사 성장인자 1 수용체 억제제(IGF-1R)인 테프로툼맙은 중국 햄스터 난소(CHO-DG44) 세포에서 생산되는 완전 인간 IgG1 단클론 항체로서 분자량은 약 148KD입니다.
테프로툼맙의 대사는 완전히 밝혀지지 않았지만, 단백질 분해에 의한 대사가 예상됩니다. 주사용 TEPEZZA는 무균, 무방부제, 백색 또는 회색의 동결건조 분말로 공급되며 정맥주사에 사용됩니다. 각 1회분 바이알에는 테프로툼맙 500mg, L-히스티딘(7.45mg), L-히스티딘 염산염 일수화물(31.8mg), 폴리솔베이트 20(1mg) 및 트레할로스 이수화합물(946mg)이 포함되어 있으며, 멸균된 주사용수(USP) 10mL로 재구성한 후 최종 농도는 47.6mg/mL, pH는 5.5입니다.
주요 7 시장(미국·독일·프랑스·이탈리아·스페인·영국·일본)의 그레이브스 안병증용 TEPEZZA에 대해 조사분석했으며, 작용기서, 용법과 용량, 연구개발 활동에 관한 인사이트, 매출의 예측 등을 제공하고 있습니다.
"TEPEZZA Market Size, Forecast, and Market Insight - 2032" report provides comprehensive insights about TEPEZZA for Graves' Ophthalmopathy in the seven major markets. A detailed picture of the TEPEZZA for Graves' Ophthalmopathy 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 TEPEZZA for Graves' Ophthalmopathy. 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 TEPEZZA market forecast analysis for Graves' Ophthalmopathy in the 7MM, SWOT, analysts' views, comprehensive overview of market competitors, and brief about other emerging therapies in Graves' Ophthalmopathy.
Teprotumumab, an insulin-like growth factor-1 receptor inhibitor (IGF-1R), is a fully human IgG1 monoclonal antibody produced in Chinese hamster ovary (CHO-DG44) cells with a molecular weight of approximately 148 KD.
The metabolism of teprotumumab has not been fully characterized; however, it is expected to undergo metabolism via proteolysis. TEPEZZA for injection is supplied as a sterile, preservative-free, and white to off-white, lyophilized powder for IV infusions. Each single-dose vial contains 500 mg of teprotumumab, L-histidine (7.45 mg), L-histidine hydrochloride monohydrate (31.8 mg), polysorbate 20 (1 mg), and trehalose dihydrate (946 mg). After reconstitution with 10 mL of sterile water for injection, USP, the final concentration is 47.6 mg/mL with a pH of 5.5.
The recommended dose of TEPEZZA is an IV infusion of 10 mg/kg for the initial dose, followed by an IV infusion of 20 mg/kg every 3 weeks for seven additional infusions.
Teprotumumab's mechanism of action in patients with Graves' Ophthalmopathy has not been fully characterized. It binds to IGF-1R and blocks its activation and signaling.
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.
TEPEZZA Analytical Perspective by DelveInsight
This report provides a detailed market assessment of TEPEZZA for Graves' Ophthalmopathy 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.
The report provides the clinical trials information of TEPEZZA for Graves' Ophthalmopathy covering trial interventions, trial conditions, trial status, start and completion dates.