A ligand binding assay (LBA) is a highly sensitive and specific analytical method used to detect and quantify biomolecules—such as proteins, peptides, or antibodies—by measuring their interaction with a target ligand. LBAs are a cornerstone of bioanalytical testing in clinical trials, particularly for biologics and other complex therapeutics.
LBAs offer several key advantages:
These benefits make LBAs essential tools for evaluating drug efficacy, safety, and patient response throughout the clinical development lifecycle.
Small Molecule and other drugs without specific epitopes an antibody can recognize (drugs with complex metabolite profiles and similarity to endogenous molecules). Oftentimes unique genetic signatures inherent to cell and gene therapies can best be characterized via PCR or sequencing.
At Eurofins Clinical Trial Solutions, we bring deep scientific expertise and cutting-edge technology to every ligand binding assay we perform. Our global network of GLP- and GCLP-compliant laboratories is equipped to support all phases of clinical development, from early-phase trials to post-marketing surveillance.
We offer:
Whether you're developing monoclonal antibodies, biosimilars, or novel biologics, we deliver the precision and reliability you need to advance with confidence.
Partner with Eurofins Clinical Trial Solutions to unlock the full potential of your clinical trial data.