Initial human experience with MK-462 (rizatriptan): a novel 5-HT1D agonist.

D G Sciberras, W J Polvino, B J Gertz, H Cheng, M Stepanavage, J Wittreich, T Olah, M Edwards, T Mant

Merck Research Laboratories, Rahway, New Jersey, USA.

British journal of clinical pharmacology 1997 Jan

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We evaluated the pharmacokinetics and pharmacodynamics of oral MK-462 in comparison with oral sumatriptan in healthy male volunteers. Sixteen healthy male volunteers were studied in a rising, single dose, alternating panel design with eight subjects per panel. Matching placebo was administered to two of eight study subjects at each dose level of MK-462 in a randomized, double-blind fashion. MK-462 was rapidly absorbed with a median tmax of 1.3 h (range 1-3 h) vs a tmax for sumatriptan of 2.5 h (range 1-4 h, P < 0.001). Administration of either MK-462 or sumatriptan produced maximal mean elevations of 5-10 mmHg in systolic and diastolic blood pressures without effect on heart rate; the changes occurred sooner following MK-462, consistent with more rapid absorption. Both MK-462 and sumatriptan provoked mild increases in serum growth hormone without any effect on serum prolactin concentrations. The most commonly reported symptom following MK-462 was drowsiness. These results indicate that the novel 5-HT1D agonist, MK-462, is rapidly absorbed following oral administration and warrants further investigation of its utility in the treatment of acute migraine.

Citation

D G Sciberras, W J Polvino, B J Gertz, H Cheng, M Stepanavage, J Wittreich, T Olah, M Edwards, T Mant. Initial human experience with MK-462 (rizatriptan): a novel 5-HT1D agonist. British journal of clinical pharmacology. 1997 Jan;43(1):49-54