Toxicology and Pharmacology Branch (TPB) Resources
TPB Resources
The TPB plans and directs collaborative, extramural and contract-supported programs involved in anti-cancer drug discovery that:
- develop methodologies to determine levels of drugs and/or their metabolites in relevant biological conditions.
- determine the pharmacokinetic profile for drugs of interest across various species.
- integrate pharmacological and biological effect data into the drug development process in order to minimize undesirable toxicity and to achieve effective drug levels.
- characterize the toxicological profile of new and established anti-tumor and antiviral agents and their modes of action in appropriate experimental settings.
- guide the development of special target organ toxicity assays.
- provide assistance for the evaluation of toxicity for biological agents and experimental formulations.
- evaluate the toxicity and safety measures for potential new vaccines to be used for immunization against cancer.
- determine the mechanism of action for high priority anti-tumor agents within relevant biological settings.
- conduct current literature surveillance for new toxicological and pharmacological evaluations which are applicable to the needs of the Institute.
- summarize all pharmacology and toxicology data for the Division of Cancer Treatment and Diagnosis (DCTD) and make recommendations about target organ toxicity and safe starting doses for Phase I clinical trials.
- provide pharmacological and toxicological inputs and assessments necessary for the preparation of Investigational New Drug Applications (IND) and Drug Master Files (DMF).
- interact with other institute centers (ICs) to exchange information on preclinical pharmacology and toxicology data pertinent to formulating recommendations for doses, dose escalation schemes and treatment schedules for clinical trials.