Antimicrob Agents Chemother. 1998 Nov;42(11):2784-91. Unique Identifier
The pharmacokinetic interaction between indinavir and ritonavir was
evaluated in five groups of healthy adult volunteers to explore the
potential for twice-daily (b.i.d.) dosing of this combination. All
subjects received 800 mg of indinavir every 8 h (q8h) on day 2. In
addition, subjects in group I received one dose of 800 mg of indinavir
on day 1 and 800 mg of indinavir q8h on day 17. Subjects in Groups II
and IV each received one dose of 600 mg of indinavir on days 1 and 17,
and subjects in groups III and V each received one dose of 400 mg of
indinavir on days 1 and 17. During days 3 to 17, ritonavir placebo or
ritonavir at 200, 300, 300, or 400 mg q12h was given to groups I, II,
III, IV, and V, respectively. Ritonavir at steady state probably
inhibited the cytochrome P-450 3A metabolism of indinavir and
substantially increased plasma indinavir concentrations, with the area
under the plasma concentration-time curve (AUC) increasing up to 475%
and the peak concentration in serum (Cmax) increasing up to 110%. The
Cmax/trough concentration ratio decreased from 50 in standard q8h
regimens to less than 14 when indinavir was administered with ritonavir.
For a constant indinavir dose, an increase in the ritonavir dose yielded
similar indinavir AUCs, Cmaxs, and concentrations at 12 h (C12s). For a
constant ritonavir dose, an increase in the indinavir dose resulted in
approximately proportional increases in the indinavir AUC, less than
proportional increases in Cmax, and slightly more than proportional
increases in C12. Ritonavir reduced between-subject variability in the
indinavir AUC and trough concentrations and did not affect indinavir
renal clearance. With the altered pharmacokinetic profile, indinavir
likely could be given as a b.i.d. combination regimen with ritonavir.
This could potentially improve patient compliance and thereby reduce
treatment failures.
JOURNAL ARTICLE Adolescence Adult Anti-HIV
Agents/*PHARMACOLOGY/PHARMACOKINETICS Dose-Response Relationship, Drug
Drug Administration Schedule Drug Interactions Drug Therapy,
Combination Female Human HIV Protease
Inhibitors/*PHARMACOLOGY/PHARMACOKINETICS Indinavir/ADVERSE
EFFECTS/*PHARMACOKINETICS Male Middle Age Models, Biological
Ritonavir/ADVERSE EFFECTS/*PHARMACOLOGY/PHARMACOKINETICS
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