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시장보고서
상품코드
1804269
세계의 RS 바이러스(RSV) 치료 시장 : 약제 유형별, 제형별, 지역별 - 시장 규모, 산업 역학, 기회 분석, 예측(2025-2033년)Global Respiratory Syncytial Virus Treatment Market: Drug Type, Dosage Form, Region-Market Size, Industry Dynamics, Opportunity Analysis and Forecast for 2025-2033 |
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세계 RS 바이러스(RSV) 치료제 시장은 RSV가 공중보건의 큰 문제라는 인식이 전 세계에서 확산되고 있음을 반영하여 빠르고 큰 폭의 성장세를 보이고 있습니다. 2024년 시장 규모는 약 23억 8,720만 달러로, 향후 10년간 대폭 확대하며, 2033년까지 83억 3,250만 달러에 달할 것으로 예측됩니다. 이 인상적인 성장은 예측 기간의 CAGR로 14.9%입니다. RSV 백신 도입 증가, 진단 인프라 강화, RSV 질환에 대한 사회적 인식과 임상적 인식 증가 등 여러 요인이 이 같은 확산을 촉진하고 있습니다.
현재 북미가 세계 RSV 치료제 시장을 주도하고 있으며, 백신 조기 승인, 연구개발에 대한 막대한 자금 지원, 광범위한 질병 관리 및 예방 활동을 지원할 수 있는 탄탄한 의료 인프라의 혜택을 누리고 있습니다. 특히 미국에서는 RSV가 특히 영유아나 노약자 등 취약 계층에게 심각한 건강상의 문제를 야기하고 있습니다. 미국 질병예방통제센터(CDC)가 2024년에 발표한 추정치에 따르면 RSV는 연간 360만-650만 명의 외래 환자, 19만-35만 명의 입원 환자, 그리고 최대 2만 3,000명의 사망을 유발하는 것으로 나타났습니다. 이러한 놀라운 수치는 효과적인 예방 및 치료 전략의 필요성을 지원합니다.
RS 바이러스(RSV) 백신 시장에서는 효과적인 RSV 예방 전략의 중요성이 높아짐에 따라 유명한 제약 및 생명공학 기업이 적극적으로 기술 혁신을 추진하고 있습니다. Moderna, Sanofi, GSK, AstraZeneca, Pfizer, Enanta Pharmaceuticals, Bavarian Nordic, Novavax, BlueWillow Biologics 등 주요 기업은 다양한 연령대의 RSV 예방에 대한 미충족 수요를 충족시키기 위해 새로운 백신 개발 및 임상연구에 앞장서고 있습니다. 미충족 수요에 대응하기 위해 새로운 백신 개발 및 임상연구의 최전선에 서 있습니다.
최근 수년간의 발전의 두드러진 예로는 Pfizer의 ABRYSVO가 있습니다. ABRYSVO는 2025년 4월 1일 유럽연합(EU)으로부터 18세-59세 성인의 하기도 질환에 대한 적응증을 승인받았습니다. 이번 승인은 3상 임상시험인 MONet 연구(NCT05842967)의 데이터를 통해 ABRYSVO가 강력한 안전성 프로파일과 우수한 내약성, 견고한 면역반응을 유발하는 것으로 입증되었습니다. 이번 규제 마일스톤을 통해 ABRYSVO는 18세 이상의 성인뿐만 아니라 생후 6개월 미만의 영아에게도 모체 접종을 통해 접종할 수 있는 EU에서 가장 광범위한 RSV 예방 효과를 제공하는 백신이 되었습니다.
Pfizer의 발전과 더불어 Clover Biopharmaceuticals도 RSV 백신 분야에서 큰 진전을 이루었습니다. 2025년 3월 23일, 클로버는 미국 식품의약국(FDA)으로부터 백신 후보물질 SCB-1019의 임상 1상 시험 개시 허가를 받았습니다. 이 임상시험은 이미 승인된 RSV 백신인 GSK의 AREXVY를 접종한 노인을 대상으로 SCB-1019의 부스터 효과를 평가하는 것을 목적으로 합니다.
주요 성장 촉진요인
RS 바이러스(RSV)는 여전히 전 세계에서 큰 보건 문제로 남아 있으며, 특히 영유아에게 심각한 영향을 미치고 있습니다. 이 바이러스는 취약한 집단에서 하기도 감염의 주요 원인 중 하나이며, 종종 의학적 개입이 필요한 중증 질환을 유발합니다. 미국에서만 RSV는 5세 미만 어린이가 연간 210만 건의 외래 진료를 받는 원인으로 추정되며, 이는 RSV가 널리 퍼져 있는 감염증의 특성을 잘 보여줍니다.
RSV로 인한 입원 또한 이 부담의 심각한 측면을 나타내며, 미국에서만 매년 5세 미만 어린이 5,000명에서 8,000명이 입원하고 있습니다. 이러한 입원은 심각한 호흡곤란, 기관지염, 폐렴 등의 합병증을 동반하는 경우가 많으며, 엄격한 모니터링과 지지요법이 필요합니다. 입원이 많다는 것은 유아의 RSV 감염의 심각성을 반영할 뿐만 아니라 의료비 및 자원 사용 증가의 원인이 되기도 합니다.
세계의 RS 바이러스(RSV) 치료 시장에 대해 조사분석했으며, 각 부문 시장 규모와 예측, 시장 역학과 동향, 기업 개요 등을 제공하고 있습니다.
The global respiratory syncytial virus (RSV) treatment market is experiencing rapid and substantial growth, reflecting the increasing recognition of RSV as a major public health challenge worldwide. Valued at approximately USD 2,387.2 million in 2024, the market is projected to expand significantly over the coming decade, reaching an estimated USD 8,332.5 million by 2033. This impressive growth corresponds to a compound annual growth rate (CAGR) of 14.9% during the forecast period. Several factors are driving this expansion, including the rising adoption of RSV vaccines, enhancements in diagnostic infrastructure, and growing public and clinical awareness of the disease.
North America currently leads the global RSV treatment market, benefiting from a combination of early vaccine approvals, substantial funding for research and development, and a well-established healthcare infrastructure capable of supporting widespread disease management and prevention efforts. In the United States specifically, RSV continues to pose a significant health concern, particularly for vulnerable populations such as infants and the elderly. According to estimates from the Centers for Disease Control and Prevention (CDC) in 2024, RSV was responsible for between 3.6 and 6.5 million outpatient visits, 190,000 to 350,000 hospitalizations, and up to 23,000 deaths annually. These staggering figures underscore the critical need for effective prevention and treatment strategies.
Several prominent pharmaceutical and biotechnology companies are actively driving innovation in the respiratory syncytial virus (RSV) vaccine market, reflecting the growing importance of effective RSV prevention strategies. Leading players such as Moderna, Sanofi, GSK, AstraZeneca, Pfizer, Enanta Pharmaceuticals, Bavarian Nordic, Novavax, and BlueWillow Biologics are at the forefront of developing new vaccines and advancing clinical research to address the unmet needs in RSV protection across different age groups.
A notable example of recent progress is Pfizer's ABRYSVO, which received approval from the European Union on April 1, 2025, for use in adults aged 18 to 59 years with lower respiratory tract disease. This approval was supported by data from the Phase 3 MONet trial (NCT05842967), which demonstrated that ABRYSVO has a strong safety profile, is well tolerated, and elicits a robust immune response. With this regulatory milestone, ABRYSVO has become the vaccine offering the broadest RSV protection in the EU, covering adults 18 years and older as well as infants up to six months of age through maternal immunization.
In addition to Pfizer's advances, Clover Biopharmaceuticals has also made significant strides in the RSV vaccine field. On March 23, 2025, Clover received clearance from the U.S. Food and Drug Administration (FDA) to initiate a Phase I clinical trial for its candidate vaccine SCB-1019. This trial is designed specifically to evaluate the booster efficacy of SCB-1019 in older adults who have previously been vaccinated with GSK's AREXVY, an RSV vaccine already approved for this population.
Core Growth Drivers
Respiratory syncytial virus (RSV) remains a major global health challenge, with a particularly profound impact on infants and young children. This virus is one of the leading causes of lower respiratory tract infections in this vulnerable population, often resulting in severe illness that necessitates medical intervention. In the United States alone, RSV is responsible for an estimated 2.1 million outpatient visits annually among children under the age of five, highlighting the widespread nature of the infection.
Hospitalizations due to RSV also represent a critical aspect of this burden, with between 58,000 and 80,000 children under five admitted to hospitals each year in the U.S. alone. These hospital stays are often required for cases involving severe respiratory distress or complications, such as bronchiolitis or pneumonia, which demand close monitoring and supportive care. The high number of hospital admissions not only reflects the severity of RSV infections in young children but also contributes to increased healthcare costs and resource utilization.
Emerging Opportunity Trends
The rollout of respiratory syncytial virus (RSV) vaccines represents a major advancement in the prevention of respiratory diseases, marking a significant milestone in public health efforts to protect vulnerable populations, especially infants and the elderly. These vaccines have proven effective in reducing the incidence and severity of RSV infections, which historically have posed a serious threat due to limited preventive options. Their introduction has not only improved clinical outcomes but also paved the way for innovative approaches to respiratory disease management.
Building on the success of recent RSV vaccine launches, pharmaceutical companies such as AstraZeneca and Moderna are actively developing next-generation vaccines that combine RSV protection with immunization against other significant respiratory illnesses. These combination vaccines aim to streamline immunization schedules, enhance patient compliance, and provide comprehensive protection by targeting multiple viruses simultaneously.
Barriers to Optimization
Respiratory syncytial virus (RSV) disease represents a significant health burden, particularly in low- and middle-income countries (LMICs), where it is a leading cause of severe respiratory illness and mortality among infants and young children. In these regions, the impact of RSV is particularly devastating due to limited access to healthcare resources, insufficient infrastructure, and the vulnerability of young populations.
The virus contributes to high rates of hospitalization and long-term respiratory complications, placing immense strain on families and healthcare systems already stretched thin by other public health challenges. Addressing RSV in LMICs is therefore a critical priority for reducing childhood morbidity and mortality. For example, recently approved drugs such as Beyfortus and Abrysvo, which offer promising protection against RSV, are priced at levels that are prohibitive for many families and healthcare providers operating within constrained budgets. Beyfortus, priced at approximately USD 414.75 per dose, and Abrysvo, costing around USD 230.00 per dose
By Dosage Form, injectables currently dominate the dosage form segment, holding an overwhelming market share exceeding 85%. This dominance reflects a strong preference within the medical community and patients for injectable therapies, which are widely recognized for their rapid onset of action and high clinical efficacy. The growing acceptance and utilization of vaccines and monoclonal antibodies (mAbs) have been significant drivers behind this trend.
By Drug Type, vaccines hold a dominant position in the drug market, commanding over 50% of the total market share. This leadership is largely driven by the recent approvals of new vaccines and their expanding application across a broader range of age groups, from infants and children to adults and the elderly. The growing awareness of preventive healthcare, coupled with increased public health initiatives and vaccination campaigns, has significantly boosted demand for vaccines worldwide. As a result, this segment has experienced robust growth, becoming a major contributor to the overall market.
By Drug Type
By Dosage Forms
By Region