Long-term tolerability of telcagepant for acute treatment of migraine in a randomized trial

Kathryn M Connor; Sheena K Aurora; Tom Loeys; Messoud Ashina; Christopher Jones; Hilde Giezek; Rachid Massaad; Angela Williams-Diaz; Christopher Lines; Tony W Ho

doi:10.1111/j.1526-4610.2010.01799.x

Long-term tolerability of telcagepant for acute treatment of migraine in a randomized trial

Kathryn M Connor, Sheena K Aurora, Tom Loeys, Messoud Ashina, Christopher Jones, Hilde Giezek, Rachid Massaad, Angela Williams-Diaz, Christopher Lines, Tony W Ho

67 Citations (Scopus)

Abstract

Objective.-To evaluate the long-term tolerability of telcagepant for acute treatment of intermittent migraine attacks. Background.-Telcagepant is a calcitonin gene-related peptide (CGRP) receptor antagonist being investigated for the acute treatment of migraine. Methods.-Migraine patients were randomized 2:1 to double-blind treatment with telcagepant 280/300 mg or rizatriptan 10 mg for an acute mild, moderate, or severe migraine. Patients could administer a second dose within 2-24 hours for nonresponse or migraine recurrence. Patients could treat up to 8 attacks per month for up to 18 months. Safety assessments included spontaneous reports of adverse events and collection of vital signs, electrocardiograms, and laboratory assessments. The primary endpoint was the percentage of patients with ≥1 triptan-related adverse events in the 14-day period post dose. Results.-Of 1068 patients randomized, 641 (90%) patients treated ≥1 attack with telcagepant and 313 (88%) treated ≥1 attack with rizatriptan. A total of 19,820 attacks were treated with telcagepant (mean per patient = 31) and 10,981 with rizatriptan (mean per patient = 35). Fewer triptan-related adverse events (difference: -6.2%; 95% CI -10.4, -2.6; P <.001) and drug-related adverse events (difference: -15.6%; 95% CI -22.2, -9.0) were reported for telcagepant vs rizatriptan. The most common adverse events appeared to have generally similar incidence proportions between the treatment groups. Those with an incidence >5% in the telcagepant group were dry mouth (9.7%, rizatriptan = 13.7%), somnolence (9.2%, rizatriptan = 16.6%), dizziness (8.9%, rizatriptan = 10.2%), and nausea (9.0%, rizatriptan = 6.4%). Conclusions.-Telcagepant was generally well tolerated when administered for the acute intermittent treatment of migraine for up to 18 months. The incidences of triptan-related and drug-related adverse events favored telcagepant over rizatriptan.

Original language	English
Journal	Headache
Volume	51
Issue number	1
Pages (from-to)	73-84
Number of pages	12
ISSN	0017-8748
DOIs	https://doi.org/10.1111/j.1526-4610.2010.01799.x
Publication status	Published - Jan 2011

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@article{488acca54d95483dbee0f93a40b9b965,

title = "Long-term tolerability of telcagepant for acute treatment of migraine in a randomized trial",

abstract = "Objective.-To evaluate the long-term tolerability of telcagepant for acute treatment of intermittent migraine attacks. Background.-Telcagepant is a calcitonin gene-related peptide (CGRP) receptor antagonist being investigated for the acute treatment of migraine. Methods.-Migraine patients were randomized 2:1 to double-blind treatment with telcagepant 280/300 mg or rizatriptan 10 mg for an acute mild, moderate, or severe migraine. Patients could administer a second dose within 2-24 hours for nonresponse or migraine recurrence. Patients could treat up to 8 attacks per month for up to 18 months. Safety assessments included spontaneous reports of adverse events and collection of vital signs, electrocardiograms, and laboratory assessments. The primary endpoint was the percentage of patients with ≥1 triptan-related adverse events in the 14-day period post dose. Results.-Of 1068 patients randomized, 641 (90%) patients treated ≥1 attack with telcagepant and 313 (88%) treated ≥1 attack with rizatriptan. A total of 19,820 attacks were treated with telcagepant (mean per patient = 31) and 10,981 with rizatriptan (mean per patient = 35). Fewer triptan-related adverse events (difference: -6.2%; 95% CI -10.4, -2.6; P <.001) and drug-related adverse events (difference: -15.6%; 95% CI -22.2, -9.0) were reported for telcagepant vs rizatriptan. The most common adverse events appeared to have generally similar incidence proportions between the treatment groups. Those with an incidence >5% in the telcagepant group were dry mouth (9.7%, rizatriptan = 13.7%), somnolence (9.2%, rizatriptan = 16.6%), dizziness (8.9%, rizatriptan = 10.2%), and nausea (9.0%, rizatriptan = 6.4%). Conclusions.-Telcagepant was generally well tolerated when administered for the acute intermittent treatment of migraine for up to 18 months. The incidences of triptan-related and drug-related adverse events favored telcagepant over rizatriptan.",

author = "Connor, {Kathryn M} and Aurora, {Sheena K} and Tom Loeys and Messoud Ashina and Christopher Jones and Hilde Giezek and Rachid Massaad and Angela Williams-Diaz and Christopher Lines and Ho, {Tony W}",

note = "{\textcopyright} 2010 American Headache Society.",

year = "2011",

month = jan,

doi = "10.1111/j.1526-4610.2010.01799.x",

language = "English",

volume = "51",

pages = "73--84",

journal = "Headache",

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TY - JOUR

T1 - Long-term tolerability of telcagepant for acute treatment of migraine in a randomized trial

AU - Connor, Kathryn M

AU - Aurora, Sheena K

AU - Loeys, Tom

AU - Ashina, Messoud

AU - Jones, Christopher

AU - Giezek, Hilde

AU - Massaad, Rachid

AU - Williams-Diaz, Angela

AU - Lines, Christopher

AU - Ho, Tony W

PY - 2011/1

Y1 - 2011/1

N2 - Objective.-To evaluate the long-term tolerability of telcagepant for acute treatment of intermittent migraine attacks. Background.-Telcagepant is a calcitonin gene-related peptide (CGRP) receptor antagonist being investigated for the acute treatment of migraine. Methods.-Migraine patients were randomized 2:1 to double-blind treatment with telcagepant 280/300 mg or rizatriptan 10 mg for an acute mild, moderate, or severe migraine. Patients could administer a second dose within 2-24 hours for nonresponse or migraine recurrence. Patients could treat up to 8 attacks per month for up to 18 months. Safety assessments included spontaneous reports of adverse events and collection of vital signs, electrocardiograms, and laboratory assessments. The primary endpoint was the percentage of patients with ≥1 triptan-related adverse events in the 14-day period post dose. Results.-Of 1068 patients randomized, 641 (90%) patients treated ≥1 attack with telcagepant and 313 (88%) treated ≥1 attack with rizatriptan. A total of 19,820 attacks were treated with telcagepant (mean per patient = 31) and 10,981 with rizatriptan (mean per patient = 35). Fewer triptan-related adverse events (difference: -6.2%; 95% CI -10.4, -2.6; P <.001) and drug-related adverse events (difference: -15.6%; 95% CI -22.2, -9.0) were reported for telcagepant vs rizatriptan. The most common adverse events appeared to have generally similar incidence proportions between the treatment groups. Those with an incidence >5% in the telcagepant group were dry mouth (9.7%, rizatriptan = 13.7%), somnolence (9.2%, rizatriptan = 16.6%), dizziness (8.9%, rizatriptan = 10.2%), and nausea (9.0%, rizatriptan = 6.4%). Conclusions.-Telcagepant was generally well tolerated when administered for the acute intermittent treatment of migraine for up to 18 months. The incidences of triptan-related and drug-related adverse events favored telcagepant over rizatriptan.

AB - Objective.-To evaluate the long-term tolerability of telcagepant for acute treatment of intermittent migraine attacks. Background.-Telcagepant is a calcitonin gene-related peptide (CGRP) receptor antagonist being investigated for the acute treatment of migraine. Methods.-Migraine patients were randomized 2:1 to double-blind treatment with telcagepant 280/300 mg or rizatriptan 10 mg for an acute mild, moderate, or severe migraine. Patients could administer a second dose within 2-24 hours for nonresponse or migraine recurrence. Patients could treat up to 8 attacks per month for up to 18 months. Safety assessments included spontaneous reports of adverse events and collection of vital signs, electrocardiograms, and laboratory assessments. The primary endpoint was the percentage of patients with ≥1 triptan-related adverse events in the 14-day period post dose. Results.-Of 1068 patients randomized, 641 (90%) patients treated ≥1 attack with telcagepant and 313 (88%) treated ≥1 attack with rizatriptan. A total of 19,820 attacks were treated with telcagepant (mean per patient = 31) and 10,981 with rizatriptan (mean per patient = 35). Fewer triptan-related adverse events (difference: -6.2%; 95% CI -10.4, -2.6; P <.001) and drug-related adverse events (difference: -15.6%; 95% CI -22.2, -9.0) were reported for telcagepant vs rizatriptan. The most common adverse events appeared to have generally similar incidence proportions between the treatment groups. Those with an incidence >5% in the telcagepant group were dry mouth (9.7%, rizatriptan = 13.7%), somnolence (9.2%, rizatriptan = 16.6%), dizziness (8.9%, rizatriptan = 10.2%), and nausea (9.0%, rizatriptan = 6.4%). Conclusions.-Telcagepant was generally well tolerated when administered for the acute intermittent treatment of migraine for up to 18 months. The incidences of triptan-related and drug-related adverse events favored telcagepant over rizatriptan.

U2 - 10.1111/j.1526-4610.2010.01799.x

DO - 10.1111/j.1526-4610.2010.01799.x

M3 - Journal article

SN - 0017-8748

VL - 51

SP - 73

EP - 84

JO - Headache

JF - Headache

IS - 1

ER -

Long-term tolerability of telcagepant for acute treatment of migraine in a randomized trial

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