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Emerging PEGylated non-biologic drugs
Eun Ji Park1,2, Jiyoung Choi1, Kang Choon Lee2,3
1a College of Pharmacy , Chung-Ang University , Seoul , Republic of Korea.
Polyethylene glycol (PEG)ylation enhances drug value, with over 18 approved products. Recent developments focus on PEGylating non-biologic drugs like small molecules and peptides for extended therapeutic effects.
Area of Science:
- Pharmaceutical Sciences
- Biotechnology
- Drug Delivery
Background:
- PEGylation, attaching polyethylene glycol (PEG), is a key technology for enhancing drug therapeutic value.
- Over 18 PEGylated products, including enzymes and proteins, are approved by the FDA.
- While biologics dominate, PEGylation is increasingly applied to non-biologic drugs.
Purpose of the Study:
- To review recent advancements in PEGylating non-biologic drugs.
- To highlight the development of PEGylated small organic molecules, synthetic peptides, and aptamers.
- To discuss the market potential and challenges of PEGylated non-biologic therapeutics.
Main Methods:
- Literature review of recent developments in PEGylation technology.
- Analysis of approved PEGylated products and those in clinical development.
- Examination of therapeutic applications and market trends for PEGylated drugs.
Main Results:
- PEGylation is expanding beyond biologic drugs to include small molecules, synthetic peptides, and aptamers.
- Numerous PEGylated non-biologic drugs, including anti-cancer agents and receptor agonists, are in development.
- PEGylation remains a commercially viable strategy for developing long-acting drug formulations.
Conclusions:
- PEGylation of non-biologic drugs represents a significant area of pharmaceutical innovation.
- Emerging PEGylated non-biologic drugs are poised to impact the market significantly.
- Despite some safety considerations, PEGylation continues to be a valuable approach for drug half-life extension.
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