The Clinical Research Unit supports the following protocols, whether conducted with inpatients or outpatients:
- First-In-Man
- Safety and Tolerability
- Pharmacokinetics Produced by Either Single or Multiple Dose Schedules
- Pharmacokinetic-Pharmacodynamic Integration
- Dose Escalation/Dose Ranging (e.g., alteration in the dose of drug administered during the study)
- Food Interaction
- Bioavailability
- Bioequivalence
- Metabolic Clearance
- Phase II and Phase III Multicenter Efficacy
