The preclinical assets market involves compound
optimization, lead identification, target validation, and assays related to
drug discovery and development prior to the initiation of human clinical
trials. Preclinical assets including chemical compounds, biologics and drug
targets play a pivotal role in early drug development and screening. Factors
such as rising R&D expenditures by pharmaceutical & biotechnology
companies and increasing government funding for preclinical research have
fueled market growth.
Preclinical
Assets Market is estimated to be valued at US$ 1.2 Billion in 2024 and is
expected to exhibit a CAGR of 7.5% over the forecast period 2024-2031.
Key Takeaways
Key players operating in the preclinical assets market are Merck & Co,
Pfizer Inc, Eli Lilly and Company, Thermo Fisher Scientific, GE Healthcare.
The rising prevalence of chronic diseases and increasing
Preclinical
Assets Market Demand for targeted therapies are projected to create new
opportunities for preclinical assets across multiple therapeutic areas in the
coming years. Technological advancements such as artificial intelligence-based
drug discovery platforms are enabling faster preclinical research and
development of innovative drugs.
Market Drivers
Rising expenditure on pharmaceutical R&D activities is a major growth
driver for the preclinical assets market. Pharmaceutical companies are
aggressively investing in early stage research to develop breakthrough drugs
and stay ahead of competition. According to a report, global spending on
pharmaceutical R&D totaled over $200 billion in 2021, a substantial
increase from the previous five years. This high investment in drug discovery
is fueling demand for preclinical assets.
Current
challenges in Preclinical Assets Market
The
Preclinical
Assets Market Size and Trends faces various challenges. Regulatory
compliances have become more stringent over the years which increases R&D
costs and duration for companies. There is also a shortage of specialized
skilled workforce required for preclinical testing. The testing process
involves complex procedures and analysis which require expertise. This shortage
can delay programs. Additionally, alternative testing methods like use of organ
on chips are still under development which can potentially reduce reliance on
animal models. Overall, companies need to balance regulatory requirements with
costs and timelines to progress assets efficiently in this market.
SWOT Analysis
Strength: Preclinical testing helps evaluate safety and efficacy at an early
stage to avoid costly failures in clinical trials. It allows selecting the most
promising candidates.
Weakness: Complete substitution of animal models is not yet possible which
faces ethical concerns. Results from animal studies may not always translate to
humans.
Opportunity: Advancements in areas like organ-on-chips, microdosing and
biomarkers are improving prediction of human response without use of large
number of animals. This can enhance efficiency.
Threats: Stricter regulatory norms increase compliance burden. Shortage of
specialized skills and alternative testing methods still maturing can lead to
delays and costs.
In terms of value, the preclinical assets market is currently concentrated in
North America and Europe due to presence of major pharmaceutical companies and
contract research organizations (CROs) in these regions. However, over the
coming years, Asia Pacific region is expected to be the fastest growing market.
This is driven by increasing R&D investment from pharmaceutical firms
looking to leverage lower costs and growing expertise in countries like China
and India. Establishment of international CROs in these regions is also
boosting preclinical development activities.
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Assets Market
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About
Author:
Ravina
Pandya, Content
Writer, has a strong foothold in the market research industry. She specializes in
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(https://www.linkedin.com/in/ravina-pandya-1a3984191)
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