Abstract
CPA was well tolerated at all dose levels (10-150 mg) following single oral dose administration to healthy male volunteers. There was no relationship between the intensity, duration and number of adverse events reported and the dose of CPA. There was a dose-related increase in exposure as measured by AUC(0-∞) and C(max). Administration of 10 mg CPA following food resulted in a delayed t(max), and a significant decrease in C(max) but not AUC(0-∞).
Original language | English |
---|---|
Pages (from-to) | 49-55 |
Number of pages | 7 |
Journal | Agents and Actions Supplements |
Volume | 49 |
Publication status | Published - 12 Dec 1997 |