| Literature DB >> 10981628 |
Abstract
Many early drug candidates derived from biotechnology failed in clinical trials because of their low affinity/specificity, short half-lives or immunogenicity. Protein engineering techniques have been applied to circumvent some of the problems that hindered these earlier trials, resulting in clinical benefits from a range of engineered antibodies and other proteins.Mesh:
Substances:
Year: 2000 PMID: 10981628 DOI: 10.1016/s0959-440x(00)00108-1
Source DB: PubMed Journal: Curr Opin Struct Biol ISSN: 0959-440X Impact factor: 6.809