Key result
TCV-116 suppresses angiotensin-II pressor response for 24 hours and reduces aldosterone response ~52%.
Why the study?
The angiotensin-II antagonistic potency and duration of effect of TCV-116 in normotensive subjects were evaluated to understand its impact on blood pressure regulation.
Does TCV-116 inhibit the pressor and aldosterone responses to angiotensin-II in normotensive subjects?
Does TCV-116 inhibit the pressor and aldosterone responses to angiotensin-II in normotensive subjects?
TCV-116 is a potent, long-lasting angiotensin-II receptor antagonist that effectively suppresses pressor and aldosterone responses in humans.
May support once-daily ARB dosing in trials; leaves open efficacy and safety in hypertensive patients.
TCV-116 is an orally active, nonpeptide antagonist of angiotensin-II type-1 receptor. The angiotensin-II antagonistic potency of TCV-116 was evaluated in normal volunteers. TCV-116 was administered at single doses of 1, 2.5, and 5 mg orally on separated days. Before, and 4, 8, and 24 h after the drug administration, angiotensin-II was infused intravenously at the rate of 2.5 to 40 ng/kg/min for 5 min each. At 2.5 mg of TCV-116, the pressor response to angiotensin-II was significantly suppressed at 4 and 8 hours after drug administration. TCV-116 at 5 mg produced a reduction of basal blood pressure and a suppression of pressor response to angiotensin-II, which persisted for 24 h. Aldosterone response to exogenous angiotensin-II was suppressed to 10% at 8 h after 5 mg of TCV-116 administration and remained suppressed to 48% until 24 h. These results suggest that TCV-116 is a highly potent and long-lasting antagonist of angiotensin-II receptor in man. The renin-angiotensin system may play a role in the regulation of blood pressure even in normotensive subjects.
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Ogihara et al. (1995) studied Normotensive. TCV-116 vs. Baseline (before drug administration) was evaluated on Pressor and aldosterone responses to angiotensin-II. TCV-116 at 5 mg suppressed the pressor response to angiotensin-II for 24 hours and reduced the aldosterone response to 10% at 8 hours and 48% at 24 hours in normotensive subjects.
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