市場調查報告書
商品編碼
1570597
促紅血球生成素藥物市場、機會、成長動力、產業趨勢分析與預測,2024-2032Erythropoietin Drugs Market, Opportunity, Growth Drivers, Industry Trend Analysis and Forecast, 2024-2032 |
2023 年,全球促紅血球生成素藥物市值約為 104 億美元,預計 2024 年至 2032 年複合年成長率為 4.5%。它們複製促紅血球生成素的功能,促紅血球生成素是一種來自腎臟的激素,負責控制紅血球的生成。這些藥物主要治療貧血,這是一種以紅血球缺乏為特徵的疾病。
癌症盛行率的上升極大地推動了市場的發展。世界衛生組織(WHO) 報告稱,2022 年全球預計將新增2000 萬癌症病例和970 萬人死亡。 這凸顯了對促紅血球生成素藥物的需求激增,促紅血球生成素藥物對於管理與治療相關的貧血至關重要,從而改善患者的治療結果和生活品質。
促紅血球生成素藥物配方的創新徹底改變了貧血管理。這些進步優先考慮提高促紅血球生成素治療的療效,確保安全性並提高患者的便利性。最近的製劑,如促紅血球生成素藥物的緩釋版本,可以減少給藥頻率。例如,達貝泊汀-阿爾法的半衰期延長,使得注射時間可以從先前的每週注射間隔延長到每兩到三週一次。
促紅血球生成素藥物產業分為藥品類型、藥品類別、用途、配銷通路和地區。
市場將藥物類型分為生物相似藥、第一代製劑和第二代製劑。預測表明,到 2032 年,生物相似藥市場規模將達到 70 億美元。這種價格優勢使得促紅血球生成素療法更容易取得,特別是在資源有限或醫療費用較高的地區。生物相似藥提供了一種經濟實惠的替代方案,擴大了患者獲得重要貧血治療的機會,特別是對於那些以前無法負擔原始生物藥物的患者。
此市場將藥物類別分為阿法依泊汀、BETA 型依泊汀、阿爾法達貝泊汀等。 2023 年,促紅血球生成素-阿爾法細分市場創造了 37 億美元的收入。阿爾法依泊汀擅長刺激骨髓中的紅血球生成(紅血球生成),使其成為治療與慢性腎臟病 (CKD)、癌症化療和其他疾病相關的貧血的首選。透過增強紅血球的產生,阿法依泊汀減少或消除了輸血的必要性,輸血會帶來輸血反應和感染等風險。
到2032年,美國促紅血球生成素藥物市場規模將達到58億美元。 2020 年,美國疾病管制與預防中心 (CDC) 記錄了 1,603,844 例新癌症病例,該疾病奪走了 602,347 人的生命。
The Global Erythropoietin Drugs Market was valued at approximately USD 10.4 billion in 2023 and is projected to grow at a CAGR of 4.5% from 2024 to 2032. Erythropoietin drugs stimulate the body's production of red blood cells (RBCs). They replicate the function of erythropoietin, a hormone from the kidneys that governs RBC production. These medications primarily address anemia, a condition marked by a shortage of red blood cells.
The market is significantly driven by the rising cancer prevalence. The World Health Organization (WHO) reported an estimated 20 million new cancer cases and 9.7 million deaths globally in 2022. This highlights the surging demand for erythropoietin drugs, pivotal in managing treatment-related anemia, thereby enhancing patient outcomes and life quality.
Innovations in erythropoietin drug formulations have revolutionized anemia management. These advancements prioritize boosting efficacy for ensuring safety and enhancing patient convenience in erythropoietin therapies. Recent formulations, like the extended-release versions of erythropoietin drugs, enable less frequent dosing. For instance, darbepoetin-alfa's extended half-life allows injections to be spaced out from the previous weekly schedule to once every two or three weeks.
The erythropoietin drugs industry is divided into drug type, drug class, application, distribution channel, and region.
The market categorizes drug types into biosimilars, first-generation formulations, and second-generation formulations. Projections indicate that the biosimilars segment will hit USD 7 billion by 2032. Biosimilars generally come at a lower price than their reference biologics. This price advantage makes erythropoietin therapies more accessible, especially in regions with constrained resources or elevated healthcare expenses. Offering a budget-friendly alternative, biosimilars broaden patient access to vital anemia treatments, especially for those previously unable to afford the original biologic drugs.
The market segments drug classes into epoetin-alfa, epoetin-beta, darbepoetin-alfa, and others. In 2023, the epoetin-alfa segment generated USD 3.7 billion. Epoetin-alfa is adept at stimulating erythropoiesis (RBC production) in the bone marrow, making it a prime choice for anemia linked to chronic kidney disease (CKD), cancer chemotherapy, and other ailments. By enhancing RBC production, epoetin-alfa diminishes or negates the necessity for blood transfusions, which carry risks like transfusion reactions and infections.
U.S. erythropoietin drugs market size will touch USD 5.8 billion by 2032. The U.S. is home to a cutting-edge healthcare system, equipped with modern medical facilities and technologies for ensuring optimal management of erythropoietin drugs. In 2020, the Centers for Disease Control and Prevention (CDC) recorded 1,603,844 new cancer cases in the U.S., with the disease claiming 602,347 lives.