市场调查报告书
商品编码
1518900
合约生技药品开发和受託製造厂商的成长机会,2024-2029Growth Opportunities in Biologics Contract Development and Manufacturing Organizations, 2024-2029 |
下一代生技药品的风险共用经营模式将推动生物/CDMO 的成长并激发未来的可能性
到2023年,生技药品将占治疗产品线的44%,其中抗体和重组蛋白是主要类别。然而,这些领域的进展已经放缓,大部分扩展在异种细胞疗法、合成核酸和病毒方面。全球生技药品管道可能转向更复杂的治疗方法,包括细胞和基因疗法(CGT)、核酸疗法、ADC和双特异性抗体。专注于这些治疗的生物製药公司可能会透过缩短临床开发时间和降低销货成本(COGS)来更加重视生产具有成本效益的药物。生技药品合约开发和受託製造厂商(Bio-CDMO) 正在积极制定其製造和供应链策略,特别专注于与服务供应商合作以优化製造流程。
美国通货膨胀减少法案 (IRA) 和 BIOSECURE 法案可能会减缓对製药创新和 CDMO 服务的需求,导致全球外包动态和 CDMO 策略发生根本性变化。创业投资透过内部重组和增加现金储备来支持其医药投资组合。对 CDMO 的需求持续下降,尤其是在开发的早期阶段。然而,2023年下半年至2024年,併购交易增加,生技资金筹措和估值具备有利条件,通膨和利率趋于稳定。到 2024 年,我们预计需求将会復苏,尤其是新兴生物製药和早期开发阶段的需求。
该分析提供了全球生物/CDMO 市场的详细收益预测。预测按市场和细分市场分类,提供有价值的行业见解。我们的分析重点是透过考虑趋势、经营模式和创新策略来强调参与企业的潜在成长机会。市场区隔涵盖产品类型、细胞表现类型、模式和区域等各个方面。考虑到 COVID-19 大流行的结束和当前的全球地缘政治问题,外包需求正在放缓。 CDMO 的需求正在减少,尤其是来自规模较小的新兴生物製药公司和早期公司的需求。该分析全面检验了2024 年至 2029 年的未来趋势。还包括有关产能扩张、併购、收购和服务扩展的见解。我们也分析生物/CDMO 策略挑战、成长驱动因素、阻碍因素、收益占有率预测和商机的影响。
Risk-sharing Business Models for Next-generation Biologics Will Drive Bio-CDMO Growth and Spur Future Potential
By 2023, biologics constituted 44% of the therapeutic pipeline, with antibodies and recombinant proteins as leading categories. Nevertheless, advancements in these fields decelerated, with most of the expansion happening in heterologous cell treatments, synthetic nucleic acids, and viruses. The global biologics pipeline will shift toward more complex treatment modalities, including cell and gene therapy (CGT), nucleic acid therapy, ADC, and bispecific antibodies. Biopharmaceutical companies that focus on these treatments will strive for reduced durations for clinical development and a greater focus on cost-effectively producing drugs with lower costs of goods sold (COGS). Biologics contract development and manufacturing organizations (Bio-CDMOs) are actively framing manufacturing and supply chain strategies, with a specific emphasis on partnering with service providers to optimize the production process.
The US Inflation Reduction Act (IRA) and the BIOSECURE Act have the potential to slow down drug innovation and the demand for CDMO services, leading to radical transformations in global outsourcing dynamics and CDMO strategies. Venture capitalists are assisting their pharmaceutical portfolios by internally restructuring and extending their cash reserves. CDMOs have experienced a consistent decrease in demand, especially for the initial phases of development. However, in late 2023 and 2024, there was a rise in M&A transactions, favorable conditions for biotech financing and valuation, and a stabilization of inflation and interest rates. Demand will resurge, particularly from emerging biopharma and early-stage development, by 2024.
This Frost & Sullivan analysis provides detailed revenue forecasts for the global market of bio-CDMOs. The forecasts are categorized by market and segment, offering valuable insights into the industry. The analysis focuses on highlighting the potential growth opportunities for participants by considering trends, business models, and innovative strategies. The market segments cover various aspects, such as product type, cell expression type, modality, and geographic region. Considering the end of the COVID-19 pandemic and the current global geopolitical issues, demand for outsourcing has decelerated. CDMOs are experiencing a decline in demand, particularly from small and emerging biopharmaceutical companies and those in the early stages of development. This analysis provides a comprehensive examination of future trends, covering the period between 2024 and 2029. It includes insights on capacity expansions, mergers, acquisitions, and the expansion of service offerings. The analysis also investigates the impact of strategic imperatives, growth drivers, restraints, revenue share estimates, and opportunities for bio-CDMOs.