The Molecular Pharmacology Shared Resource (MPSR) provides a wide variety of services regarding clinical and preclinical anticancer pharmacology as summarized below.
For assistance, request Molecular Pharmacology Service here (PPMS Access Required):
Signup for a new PPMS account | Quick guide for signing up
The MPSR works to develop and implement clinical PK/PD studies. The MPSR will coordinate and manage all specimen collection and processing for the trial principal investigator and develop new assays and conduct specimen analysis on demand to understand the PK/PD properties and potential of drug-drug interactions of tested agents.
Protocol and study development
Specimen acquisition and management
Specimen analysis
The MPSR can design and conduct comprehensive experiments for in vitro and in vivo testing of novel agents or therapeutic combinations for discovery and proof-of-principle. Such studies can provide rationale for clinical trial development. A wide variety of molecular pharmacological approaches, and clinically-relevant cell and xenograft animal models can be utilized.