Literature DB >> 23798725

Lack of hemodynamic interaction between CGRP-receptor antagonist telcagepant (MK-0974) and sumatriptan: results from a randomized study in patients with migraine.

M Depré1, C Macleod, J Palcza, Mo Behm, I de Lepeleire, T Han, D Panebianco, Wb Smith, R Blanchard, Ja Chodakewitz, Mg Murphy, Jn de Hoon.   

Abstract

OBJECTIVE: The objective of this article is to assess the effects of sumatriptan monotherapy, telcagepant monotherapy, and their combination on blood pressure (BP) in migraine patients during a headache-free period.
METHODS: A double-blind, placebo-controlled, four-period, single-dose, randomized crossover study in 24 migraine patients was conducted. In each period, patients received a single oral dose of sumatriptan 100 mg alone, telcagepant 600 mg alone, sumatriptan 100 mg coadministered with telcagepant 600 mg, or placebo. Semi-recumbent BP was measured pre-dose and at seven post-dose time points over a period of six hours. Individual time-weighted averages in mean arterial pressure (MAP) were evaluated using a linear mixed-effects model. The pharmacokinetics of sumatriptan alone and in the presence of telcagepant were also evaluated using limited sampling times.
RESULTS: The mean difference in time-weighted (0-2.5 h) MAP (90% confidence interval) was 1.2 mmHg (-0.2, 2.7) between telcagepant and placebo, 4.0 mmHg (2.5, 5.5) between sumatriptan and placebo, and 1.5 mmHg (0.0, 3.0) between telcagepant with sumatriptan vs sumatriptan alone. When coadministered with telcagepant, the AUC0-6h and C(max) of sumatriptan were increased by 23% and 24%, respectively. The small MAP increases observed after coadministration could possibly be associated with the slight elevations in sumatriptan levels.
CONCLUSION: Telcagepant does not elevate mean MAP, and coadministration of telcagepant with sumatriptan results in elevations in MAP similar to those observed following administration of sumatriptan alone in migraineurs during the interictal period. When coadministered, telcagepant slightly increases the plasma levels of sumatriptan, but without an apparent clinically meaningful effect.

Entities:  

Keywords:  CGRP receptor antagonist; Triptan; blood pressure; migraine; sumatriptan; telcagepant

Mesh:

Substances:

Year:  2013        PMID: 23798725     DOI: 10.1177/0333102413494272

Source DB:  PubMed          Journal:  Cephalalgia        ISSN: 0333-1024            Impact factor:   6.292


  4 in total

Review 1.  From LBR-101 to Fremanezumab for Migraine.

Authors:  Marcelo E Bigal; Alan M Rapoport; Stephen D Silberstein; Sarah Walter; Richard J Hargreaves; Ernesto Aycardi
Journal:  CNS Drugs       Date:  2018-11       Impact factor: 5.749

Review 2.  Calcitonin gene-related peptide: physiology and pathophysiology.

Authors:  F A Russell; R King; S-J Smillie; X Kodji; S D Brain
Journal:  Physiol Rev       Date:  2014-10       Impact factor: 37.312

3.  Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of the CGRP Binding Monoclonal Antibody LY2951742 (Galcanezumab) in Healthy Volunteers.

Authors:  David Monteith; Emily C Collins; Corinne Vandermeulen; Anne Van Hecken; Eyas Raddad; Joel C Scherer; David Grayzel; Thomas J Schuetz; Jan de Hoon
Journal:  Front Pharmacol       Date:  2017-10-17       Impact factor: 5.810

4.  Phase 1, randomized, parallel-group, double-blind, placebo-controlled trial to evaluate the effects of erenumab (AMG 334) and concomitant sumatriptan on blood pressure in healthy volunteers.

Authors:  Jan de Hoon; Anne Van Hecken; Corinne Vandermeulen; Marissa Herbots; Yumi Kubo; Ed Lee; Osa Eisele; Gabriel Vargas; Kristin Gabriel
Journal:  Cephalalgia       Date:  2018-05-21       Impact factor: 6.292

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.