ABSTRACTReceptor occupancy assays applied in clinical studies provide insights into pharmacokinetic-pharmacodynamic relationships for therapeutic antibodies. When measured by different assays, however, receptor occupancy results can be controversial, as was observed for nivolumab, a monoclonal antibody targeting programmed cell death 1 (PD-1) receptor. We suggested an explanation of results obtained and a mechanistic approach based on specific features of the receptor occupancy assays: measurement of the free or bound receptor, normalized to the baseline or at each time point. The approach was evaluated against controversial clinical data on PD-1 receptor occupancy by nivolumab. It was shown that receptor occupancy measured by different ass...
An important question in drug discovery is how to overcome the significant challenge of high drug at...
Reversible binding, for example between signaling molecules and receptors on the cell surface, is on...
AbstractThe study of the magnitude and variation of drug response is defined as pharmacodynamics (PD...
Receptor occupancy, the ratio between amount of drug bound and amount of total receptor on single ce...
Abstract: Targeting receptor systems by competitive inhibition is the objective of various antibody ...
We consider the relationship between the target affinity of a monoclonal antibody and its in vivo po...
Monoclonal antibodies (mAbs) targeted to the programmed cell death protein 1 (PD-1) remain the most ...
We report the development and validation of a 12 parameter immunofluorescence flow cytometry method ...
Chemokine receptors play an important role in trafficking leukocytes within the body, a process that...
Cellular communication is essential for organism survival and often is initiated by the binding of a...
The study of the magnitude and variation of drug response is defined as pharmacodynamics (PDs). PD m...
The pharmacodynamics of drug-candidates is often optimized by metrics that describe target binding (...
Investigation of pharmacokinetic/pharmacodynamic (PK/PD) relationships for inhaled drugs is challeng...
Objectives: Otelixizumab is a monoclonal antibody (mAb) directed against human CD3ε, which forms par...
Predictions for target engagement are often used to guide drug development. In particular, when sele...
An important question in drug discovery is how to overcome the significant challenge of high drug at...
Reversible binding, for example between signaling molecules and receptors on the cell surface, is on...
AbstractThe study of the magnitude and variation of drug response is defined as pharmacodynamics (PD...
Receptor occupancy, the ratio between amount of drug bound and amount of total receptor on single ce...
Abstract: Targeting receptor systems by competitive inhibition is the objective of various antibody ...
We consider the relationship between the target affinity of a monoclonal antibody and its in vivo po...
Monoclonal antibodies (mAbs) targeted to the programmed cell death protein 1 (PD-1) remain the most ...
We report the development and validation of a 12 parameter immunofluorescence flow cytometry method ...
Chemokine receptors play an important role in trafficking leukocytes within the body, a process that...
Cellular communication is essential for organism survival and often is initiated by the binding of a...
The study of the magnitude and variation of drug response is defined as pharmacodynamics (PDs). PD m...
The pharmacodynamics of drug-candidates is often optimized by metrics that describe target binding (...
Investigation of pharmacokinetic/pharmacodynamic (PK/PD) relationships for inhaled drugs is challeng...
Objectives: Otelixizumab is a monoclonal antibody (mAb) directed against human CD3ε, which forms par...
Predictions for target engagement are often used to guide drug development. In particular, when sele...
An important question in drug discovery is how to overcome the significant challenge of high drug at...
Reversible binding, for example between signaling molecules and receptors on the cell surface, is on...
AbstractThe study of the magnitude and variation of drug response is defined as pharmacodynamics (PD...