Skip to Content
Developmental Therapeutics Program (DTP)
Contact DTP
Show menu
Search this site
Last Updated: 04/02/15

Toxicology and Pharmacology Primer

The following toxicology and pharmacology resources are made available only via our Pathway to Development Resources (the NExT Program).

Pharmacokinetics and ADME

Drug Plasma Method Development: Develop and validate an analytical method for quantitation of the compound in question in mouse, rat, dog, and human plasma. Characterize the stability in plasma at 37°C. If significant decomposition is observed, similar studies should be conducted at 4°C. Assess the stability in frozen plasma and/or plasma extracts to determine appropriate sample handling and storage procedures.

Determine the extent of protein binding in mouse, rat, dog, and human plasma. Additional binding studies with constituent plasma proteins (albumin, 1-AGP) may also be performed.

Pharmacokinetics: Plasma elimination kinetics will be determined in one or more of the following species: mice, rats, dogs, and non-human primates after single intravenous doses of drug. Of primary importance will be the determination of plasma levels or Area Under the Curve (AUC) associated with efficacy in tumored animal models. Other routes of administration such as oral, intraperitoneal, subcutaneous, and intramuscular may be necessary to evaluate as well. Bioavailability of non-parenteral routes and plasma clearance rates will be determined in order to establish the dose required to produce effective drug concentrations in plasma for future toxicity study evaluation. The ability of a drug to cross the blood-brain barrier will be assessed in dogs or non-human primates, as needed.

A standard mathematical work-up of the plasma concentration-time data to yield half-life values, plasma clearance, AUC, etc. will be performed. Urine may be collected in selected experiments for determination of cumulative drug excretion, urinary clearance, and possible identification of drug metabolites. Major organs and tissues may be obtained at necropsy and frozen for possible characterization of the tissue distribution of the compound.

Metabolism: For those compounds that undergo metabolism, the in vitro and in vivo metabolism will be characterized and the potential effects of this compound on drug metabolizing enzymes will also be evaluated. Initially, the metabolism by mouse, rat, and human liver microsomes will be characterized. These studies shall include, as necessary, determinations of cofactor dependency and effects of CO and N2 on metabolism.

If P450 involvement is evident, studies using cDNA-expressed P450 isoforms and/or specific substrate/inhibitors of P450 isoforms shall be performed to further characterize the enzymes responsible for metabolism.

In vivo studies in mice and/or rats may be performed to confirm and extend the preliminary investigations described above and to obtain quantities of metabolites for structure identification and comparisons with in vitro results.

If results of the in vitro and in vivo studies outlined above suggest that the compound could induce its own metabolism and/or be involved in clinically significant metabolism-based drug interactions, in vivo studies to test this hypothesis will be considered.

Toxicology Evaluation

Range Finding and Exploratory Toxicity: For each compound, it will be necessary to establish a maximum tolerated dose (MTD) and identify acute, dose limiting toxicities (DLT) in rodent and/or non-rodent species.

Investigational New Drug Application (IND)-Directed Toxicity: For each compound, it will be necessary to establish toxicity and safety in relation to drug plasma concentrations or area-under-the-curve in both a rodent and non-rodent species.

Bone Marrow Toxicity: For each drug that produces myelosuppression in preliminary toxicity studies or is an analog of a drug known to produce bone marrow toxicity, human, canine, and murine bone marrow toxicity assessments will be performed in vitro using CFUGM and correlated with toxicity that occurs in vivo. Assessment of toxicity in other bone marrow progenitors is performed as necessary.

Go to a list of TPB Supported INDs/DMFs

About the Branch Chief

Elizabeth Glaze, Ph.D., DABT Dr. Elizabeth Glaze earned her Ph.D. in Pharmacology from the University of Michigan in 1999. There she evaluated the mechanism by which 5’-bromo-2’-deoxyuridine (BrdU) sensitizes human glioma cells to DNA alkylating agents. More…