The pharmacokinetics of the antifungal pradimicin derivative BMS 181184 in plasma of normal, catheterized rabbits were characterized after single and multiple daily intravenous administrations of dosa
*VEE-R2, VEE-14/00/4, and VEE-CM243(N610Q) indicate VEE replicon particle preparations (VRP) expressing the respective gp160 coding sequences. Monkeys received either the single VRP indicated, or all
