Sydney, April 2025 – Novotech, a globally recognized full-service clinical research organization (CRO) and scientific advisory partner for biotech and small- to mid-sized pharmaceutical companies seeking to advance drug development, has released an in-depth report on the global clinical trial landscape for Idiopathic Pulmonary Fibrosis (IPF). The report offers strategic insights and comprehensive analysis critical for biotech and pharmaceutical companies navigating the complexities of IPF clinical research and drug development. 

Advancing IPF Clinical Research: A Global Perspective 

Idiopathic Pulmonary Fibrosis (IPF) is a chronic, progressive lung disease characterized by the scarring of lung tissue and a steady decline in respiratory function, most commonly affecting individuals between the ages of 60 and 70. Novotech’s latest report identifies more than 800 industry-sponsored IPF clinical trials launched globally since 2020, reflecting strong research momentum and a growing commitment across the biotech and pharmaceutical sectors to address the increasing burden of this serious condition. 

Key insights: 

  • Global Clinical Trial Activity: The Asia-Pacific region accounts for the largest share of global IPF clinical trials at 44%, primarily driven by significant activity in Mainland China. North America follows with 23%, led by the United States, while Europe contributes 21%, with notable trial concentration in the United Kingdom and Germany.
  • Emerging Therapeutic Innovations: The development pipeline is advancing with novel therapeutic approaches, including RNA interference (RNAi)-based therapies, PDE4 inhibitors, cell-based treatments, and monoclonal antibodies—signaling promising progress in IPF management and patient outcomes.
  • Advancements in Trial Design and Biomarkers: Precision medicine and patient-centric trial methodologies, coupled with the integration of key biomarkers, are improving diagnostic accuracy, disease monitoring, and the assessment of therapeutic efficacy in IPF studies.
  • Investment and Funding Landscape: Strong venture capital activity is fueling early- and mid-stage IPF drug development, particularly in the United States and Europe. Public-sector contributions, including funding from the EU Horizon 2020 program and the U.S. Department of Defense, are also instrumental in supporting innovation.
  • Addressing Racial and Ethnic Disparities: The report highlights the critical need for greater diversity in IPF clinical trials and calls for equitable care strategies and targeted education to reduce treatment disparities across racial and ethnic populations. 

Partnering with Novotech for IPF Clinical Trials 

With extensive expertise in pulmonary and respiratory diseases, Novotech offers biotech and pharmaceutical partners an accelerated path to market. The company’s comprehensive capabilities include therapeutic expertise, regulatory guidance, and strategic clinical trial execution, supported by its expansive global footprint across Asia-Pacific, North America, and Europe. 

Download the Full Report 

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关于诺为泰Novotech-CRO.com

Novotech(诺为泰)作为一家可提供全方位服务的国际性临床研究组织 (CRO) 和科学咨询公司,深受生物科技公司以及中小型制药公司的信赖,并指导其在各个阶段的药物开发。 

公司在全球范围内拥有30多个办公地点,主要分布在亚太地区、北美和欧洲,并与5000多个试验机构建立了紧密的合作关系,为客户提供丰富的临床试验资源网络,帮助客户充分利用关键试验区域,广泛接触不同的受试者群体,推动变革性疗法更快惠及患者。 

通过以客户为中心的服务模式,诺为泰无缝整合人才、流程和技术,提供定制化解决方案,加速变革疗法快速上市。通过构建紧密的合作伙伴关系,诺为泰坚定不移地支持客户实现研究目标,赋能创新,推动全球医疗健康发展。凭借在临床试验执行和创新方面的卓越表现,诺为泰已荣获多项殊荣,包括连续19年蝉联弗若斯特沙利文CRO年度公司奖 (Frost & Sullivan CRO Company of the Year)。依托深厚的临床领域与监管专业知识,结合对当地市场的深刻洞察,公司致力于简化临床试验流程,优化数据分析,并加快受试者招募策略的实施。 

我们与客户携手并进,加速科研成果的落地转化,改善全球患者结局,践行我们推动创新、实现卓越成果的使命。 

要了解更多信息或与专家团队成员交谈,请访问www.Novotech-CRO.com

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