Naratriptan Efficacy in Migraineurs Who Respond Poorly to Oral Sumatriptan

Objectives.—To determine whether 347 patients would respond to a 50‐mg oral dose of sumatriptan, even though they considered themselves poor responders to this acute therapy for migraine, and to investigate whether oral naratriptan can be an effective acute therapy for migraine in the subset of pati...

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Veröffentlicht in:Headache 2000-07, Vol.40 (7), p.513-520
Hauptverfasser: Stark, Stuart, Spierings, Egilius L.H., McNeal, Scott, Putnam, Gayla P., Bolden-Watson, Carolyn P., O'Quinn, Stephen
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container_end_page 520
container_issue 7
container_start_page 513
container_title Headache
container_volume 40
creator Stark, Stuart
Spierings, Egilius L.H.
McNeal, Scott
Putnam, Gayla P.
Bolden-Watson, Carolyn P.
O'Quinn, Stephen
description Objectives.—To determine whether 347 patients would respond to a 50‐mg oral dose of sumatriptan, even though they considered themselves poor responders to this acute therapy for migraine, and to investigate whether oral naratriptan can be an effective acute therapy for migraine in the subset of patients who did not respond to sumatriptan under double‐blind, well‐controlled conditions. Background.—Although most migraineurs respond to sumatriptan, there remains a need for an effective alternative for those who do not respond. Naratriptan is a more potent and more lipophilic member of this class of agent and could prove beneficial in such patients. This is the first well‐controlled study to assess the value of another 5‐HT1B/1D agonist in this difficult patient subset. Methods.—This study comprised two migraine attacks. The first (attack 1) was a single‐blind assessment of the efficacy of sumatriptan (50 mg orally) in patients with a history of poor response to the drug. The second (attack 2) was a randomized, parallel group, double‐blind, placebo‐controlled trial of naratriptan (2.5 mg orally) in nonresponders to oral sumatriptan. Results.—Attack 1: About two thirds of this selected migraine population did not respond to sumatriptan. Attack 2: Naratriptan was statistically superior to placebo for headache relief at 2 hours and 4 hours, as well as for most other features of migraine attacks. These data suggest an intrinsic efficacy of naratriptan in this patient subset and not a coincidental response. No unexpected tolerability issues arose. Conclusions.—Naratriptan is an alternative therapy for migraineurs who respond poorly to oral sumatriptan. No response to one “triptan” does not necessarily predict no response to them all.
doi_str_mv 10.1046/j.1526-4610.2000.00082.x
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Background.—Although most migraineurs respond to sumatriptan, there remains a need for an effective alternative for those who do not respond. Naratriptan is a more potent and more lipophilic member of this class of agent and could prove beneficial in such patients. This is the first well‐controlled study to assess the value of another 5‐HT1B/1D agonist in this difficult patient subset. Methods.—This study comprised two migraine attacks. The first (attack 1) was a single‐blind assessment of the efficacy of sumatriptan (50 mg orally) in patients with a history of poor response to the drug. The second (attack 2) was a randomized, parallel group, double‐blind, placebo‐controlled trial of naratriptan (2.5 mg orally) in nonresponders to oral sumatriptan. Results.—Attack 1: About two thirds of this selected migraine population did not respond to sumatriptan. Attack 2: Naratriptan was statistically superior to placebo for headache relief at 2 hours and 4 hours, as well as for most other features of migraine attacks. These data suggest an intrinsic efficacy of naratriptan in this patient subset and not a coincidental response. No unexpected tolerability issues arose. Conclusions.—Naratriptan is an alternative therapy for migraineurs who respond poorly to oral sumatriptan. No response to one “triptan” does not necessarily predict no response to them all.</description><identifier>ISSN: 0017-8748</identifier><identifier>EISSN: 1526-4610</identifier><identifier>DOI: 10.1046/j.1526-4610.2000.00082.x</identifier><identifier>PMID: 10940089</identifier><identifier>CODEN: HEADAE</identifier><language>eng</language><publisher>Boston, MA, USA: Blackwell Science Inc</publisher><subject>Administration, Oral ; Adult ; Biological and medical sciences ; Cardiovascular system ; Double-Blind Method ; efficacy ; Female ; Humans ; Indoles - therapeutic use ; lipophilicity ; Male ; Medical sciences ; migraine ; Migraine Disorders - drug therapy ; naratriptan ; Pharmacology. Drug treatments ; Piperidines - therapeutic use ; Prospective Studies ; Recurrence ; Serotonin Receptor Agonists - therapeutic use ; Single-Blind Method ; sumatriptan ; Sumatriptan - therapeutic use ; Treatment Outcome ; Tryptamines ; Vasodilator agents. 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Background.—Although most migraineurs respond to sumatriptan, there remains a need for an effective alternative for those who do not respond. Naratriptan is a more potent and more lipophilic member of this class of agent and could prove beneficial in such patients. This is the first well‐controlled study to assess the value of another 5‐HT1B/1D agonist in this difficult patient subset. Methods.—This study comprised two migraine attacks. The first (attack 1) was a single‐blind assessment of the efficacy of sumatriptan (50 mg orally) in patients with a history of poor response to the drug. The second (attack 2) was a randomized, parallel group, double‐blind, placebo‐controlled trial of naratriptan (2.5 mg orally) in nonresponders to oral sumatriptan. Results.—Attack 1: About two thirds of this selected migraine population did not respond to sumatriptan. Attack 2: Naratriptan was statistically superior to placebo for headache relief at 2 hours and 4 hours, as well as for most other features of migraine attacks. These data suggest an intrinsic efficacy of naratriptan in this patient subset and not a coincidental response. No unexpected tolerability issues arose. Conclusions.—Naratriptan is an alternative therapy for migraineurs who respond poorly to oral sumatriptan. 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Drug treatments</subject><subject>Piperidines - therapeutic use</subject><subject>Prospective Studies</subject><subject>Recurrence</subject><subject>Serotonin Receptor Agonists - therapeutic use</subject><subject>Single-Blind Method</subject><subject>sumatriptan</subject><subject>Sumatriptan - therapeutic use</subject><subject>Treatment Outcome</subject><subject>Tryptamines</subject><subject>Vasodilator agents. 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Attack 2: Naratriptan was statistically superior to placebo for headache relief at 2 hours and 4 hours, as well as for most other features of migraine attacks. These data suggest an intrinsic efficacy of naratriptan in this patient subset and not a coincidental response. No unexpected tolerability issues arose. Conclusions.—Naratriptan is an alternative therapy for migraineurs who respond poorly to oral sumatriptan. No response to one “triptan” does not necessarily predict no response to them all.</abstract><cop>Boston, MA, USA</cop><pub>Blackwell Science Inc</pub><pmid>10940089</pmid><doi>10.1046/j.1526-4610.2000.00082.x</doi><tpages>8</tpages></addata></record>
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subjects Administration, Oral
Adult
Biological and medical sciences
Cardiovascular system
Double-Blind Method
efficacy
Female
Humans
Indoles - therapeutic use
lipophilicity
Male
Medical sciences
migraine
Migraine Disorders - drug therapy
naratriptan
Pharmacology. Drug treatments
Piperidines - therapeutic use
Prospective Studies
Recurrence
Serotonin Receptor Agonists - therapeutic use
Single-Blind Method
sumatriptan
Sumatriptan - therapeutic use
Treatment Outcome
Tryptamines
Vasodilator agents. Cerebral vasodilators
title Naratriptan Efficacy in Migraineurs Who Respond Poorly to Oral Sumatriptan
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