Growth Opportunities in Biologics Contract Development and Manufacturing Organizations, 2024 2029

Growth Opportunities in Biologics Contract Development and Manufacturing Organizations, 2024 2029

Risk-sharing Business Models for Next-generation Biologics Will Drive Bio-CDMO Growth and Spur Future Potential

RELEASE DATE
25-Jun-2024
REGION
Global
Deliverable Type
Market Research
Research Code: PFKF-01-00-00-00
SKU: HC_2024_835
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Description

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.

Author: Surbhi Gupta

Table of Contents

Why is it Increasingly Difficult to Grow?

The Strategic Imperative 8™

The Impact of the Top 3 Strategic Imperatives on the Bio-CDMO Industry

Biologics Industry—Outlook

Biologics Industry—Key Therapeutic Area Outlook

Biologics Pipeline by Modality and Phase

Biologics Industry—Market size and Growth Rate Forecast by Modality

Global Trends Impacting the Bio-CDMO Industry

Global Trends Impacting the Bio-CDMO Industry (continued)

Industry Trends Impacting the Bio-CDMO Industry

Industry Trends Impacting the Bio-CDMO Industry (continued)

Business Model—Shift from Fee-for-service to Value-based Risk-sharing

Value-based Risk-sharing Business Model

Scope of Analysis

Segmentation

Segmentation

Competitive Environment

Key Competitors

Growth Metrics

Growth Drivers

Growth Restraints

Forecast Considerations

Forecast Framework—Bio-CDMO Market Sizing

Forecast Methodology—Bio-CDMO Market

Revenue Forecast

Revenue Forecast by Product Type

Revenue Forecast by Cell-culture Type

Revenue Forecast by Region

Revenue Forecast by Modality

Revenue Forecast Analysis

Revenue Forecast Analysis by Region

Revenue Forecast Analysis by Region (continued)

Revenue Share

Revenue Share Analysis

Growth Metrics

Revenue Forecast

Forecast Analysis

Growth Metrics

Revenue Forecast

Forecast Analysis

Growth Metrics

Revenue Forecast

Forecast Analysis

Growth Metrics

Revenue Forecast

Forecast Analysis

Growth Opportunity 1—Expanding Drug Product Capabilites to Support Anti-obesity Drugs

Growth Opportunity 1—Expanding Drug Product Capabilites to Support Anti-obesity Drugs (continued)

Growth Opportunity 2—Providing End-to-end mRNA Services

Growth Opportunity 2—Providing End-to-end mRNA Services (continued)

Growth Opportunity 3—Indian Domestic Players Enhance Biologics Capabilities

Growth Opportunity 3—Indian Domestic Players Enhance Biologics Capabilities (continued)

Best Practice Recognition

Benefits and Impacts of Growth Opportunities

Next Steps

Take the Next Step

List of Exhibits

List of Exhibits (continued)

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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. Author: Surbhi Gupta
More Information
Deliverable Type Market Research
Author Surbhi Gupta
Industries Healthcare
No Index No
Is Prebook No
Keyword 1 Biologics contract development
Keyword 2 Biologics industry advancements
Keyword 3 Biologics CDMO
Podcast No
Predecessor PDEF-01-00-00-00
WIP Number PFKF-01-00-00-00