NATIONAL CANCER INSTITUTE - CANCER.GOV

Contact Information


Primary Contact

William Douglas Figg, Sr.
Acting Chief

Location

Building 10, Room 5A01
Bethesda, MD 20892

Overview

The CPP is directly responsible for the pharmacokinetic (PK) analysis of numerous Phase I and II clinical trials conducted within the NCI. In addition, the CPP provides direct PK support for many studies performed elsewhere in the extramural community. The program provides bioanalytical support (LC-MS) and pharmacokinetic-pharmacodynamic (PK/PD) modeling and simulation of investigational agents or combination therapies to predict exposure-response in future trials (Pharmacometrics Core). The CPP can also assist with determining protein binding, drug-drug interactions, concentration-effect analysis, drug metabolism and routes of elimination for new anticancer agents.

Established Technologies

  • Bioanalytical support (LC-MS)
  • Pharmacokinetic analysis
  • Modeling of investigational agents or combination therapies
  • The CPP can also assist with determining protein binding, drug-drug interactions, concentration-effect analysis, drug metabolism and routes of elimination for new anticancer agents.

Major Instrumentation

UV/Vis spectrophotometry

HPLC-UV

HPLC-FL

LC-MS

LC-MS/MS

User Guidelines

The CPP is open to all NCI intramural clinical investigators.

Keywords

LC-MSbioanalysisPharmacologynci-corepharmacokinetics