Efficacy and tolerability of almotriptan in adolescents: A randomized, double-blind, placebo-controlled trial

被引:68
|
作者
Linder, Steven L. [1 ]
Mathew, Ninan T. [2 ]
Cady, Roger K. [3 ]
Finlayson, Gary [4 ]
Ishkanian, Gary [5 ]
Lewis, Donald W. [6 ]
机构
[1] Dallas Pediat Neurol Associates, Dallas, TX 75230 USA
[2] Houston Headache Clin, Houston, TX USA
[3] Headache Care Ctr, Springfield, MO USA
[4] Ortho McNeil Janssen Sci Affairs, Titusville, NJ USA
[5] Elkind Headache Ctr, Mt Vernon, IA USA
[6] Eastern Virginia Med Sch, Norfolk, VA 23501 USA
来源
HEADACHE | 2008年 / 48卷 / 09期
关键词
AE adverse event; GCP Good Clinical Practice; ITT intent-to-treat; SPF sustained pain-free; SPR sustained pain relief;
D O I
10.1111/j.1526-4610.2008.01138.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives.-To assess the efficacy and safety of almotriptan 6.25 mg, 12.5 mg, and 25 mg vs placebo for acute migraine treatment in adolescents. Patients and Methods.-In this double-blind, placebo-controlled, parallel-group, multicenter trial, 866 patients aged 12 to 17 years with a >1 year history of migraine (per International Headache Society criteria) were randomized to treat one migraine headache with almotriptan 6.25 mg, 12.5 mg, 25 mg, or placebo. The primary efficacy endpoint was headache pain relief 2 hours after dosing, adjusted for baseline severity, with absence of nausea, photophobia, and phonophobia 2 hours after dosing as coprimary endpoints. Results.-The 2-hour pain-relief rate was significantly higher with almotriptan 25 mg compared with placebo (66.7% vs 55.3%; P=.022). The incidence of nausea, photophobia, and phonophobia at 2 hours (adjusted for baseline pain intensity) for the almotriptan 25 mg and placebo groups was not significantly different. The 2-hour pain-relief rates (unadjusted) were significantly higher with almotriptan 6.25 mg (71.8%),12.5 mg (72.9%), and 25 mg (66.7%) than with placebo (55.3%;P=.001, P<.001, and P=.028, respectively). Rates for sustained pain relief also were significantly greater with almotriptan 6.25 mg (67.2%), 12.5 mg (66.9%), and 25 mg (64.5%) than with placebo group (52.4%), P<.01 for the 6.25- and 12.5-mg doses and P .05 for the 25-mg dose. Age group subanalysis demonstrated significantly greater 2-hour pain-relief rates with all 3 doses of almotriptan compared with placebo for patients aged 15 to 17 years, a significantly lower incidence of photophobia and phonophobia at 2 hours with almotriptan 12.5 mg compared with placebo for patients aged 15 to 17 years, and a significantly lower incidence of photophobia with almotriptan 12.5 mg compared with placebo for those aged 12 to 14 years. Almotriptan treatment was well tolerated, with the most common adverse events (>2%) of nausea, dizziness, and somnolence. Conclusions.-Oral almotriptan was efficacious for relieving migraine headache pain in adolescents, with the 12.5-mg dose associated with the most favorable efficacy profile with respect to relieving headache pain and associated symptoms of migraine (photophobia and phonophobia). Almotriptan treatment was well tolerated in this adolescent population.
引用
收藏
页码:1326 / 1336
页数:11
相关论文
共 50 条
  • [21] Cardiovascular safety and pharmacokinetics of almotriptan:: a randomized, double-blind, placebo-controlled, crossover clinical trial in healthy volunteers
    Salvà, M
    Jansat, JM
    Martínez-Tobed, A
    CEPHALALGIA, 2003, 23 (07) : 706 - 706
  • [22] Efficacy and Tolerability of Cyproheptadine in Poor Appetite: A Multicenter, Randomized, Double-blind, Placebo-controlled Study
    Kim, Sue Youn
    Yun, Jae Moon
    Lee, Ji-Won
    Cho, Young Gyu
    Cho, Kyung-Hwan
    Park, Yong Gyu
    Cho, Belong
    CLINICAL THERAPEUTICS, 2021, 43 (10) : 1757 - +
  • [23] Randomized double-blind trial comparing the efficacy and tolerability of almotriptan and zolmitriptan in the acute treatment of migraine
    Goadsby, P. J.
    Massiou, H.
    Cabarrocas, X.
    Pascual, J.
    EUROPEAN JOURNAL OF NEUROLOGY, 2005, 12 : 195 - 195
  • [24] Safety and tolerability of Ganoderma lucidum in healthy subjects:: A double-blind randomized placebo-controlled trial
    Wicks, Sheila M.
    Tong, Robin
    Wang, Chong-Zhi
    O'Connor, Michael
    Karrison, Theodore
    Li, Shang
    Moss, Jonathan
    Yuan, Chun-Su
    AMERICAN JOURNAL OF CHINESE MEDICINE, 2007, 35 (03): : 407 - 414
  • [25] Tolerability of glutamine supplementation in older adults: a double-blind placebo-controlled randomized clinical trial
    de Nobrega, T. C. M.
    da Silva, M. A. R. C. P.
    Rampani, E. M.
    Curi, R.
    Bazotte, R. B.
    BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2024, 57
  • [26] CETACAINE EFFICACY - A DOUBLE-BLIND, RANDOMIZED, PLACEBO-CONTROLLED STUDY
    LACHTER, J
    JACOBS, R
    LAVY, A
    SUISSA, A
    WEISLER, A
    EIDELMAN, S
    GASTROENTEROLOGY, 1988, 94 (05) : A245 - A245
  • [27] Marfan Sartan: a randomized, double-blind, placebo-controlled trial
    Milleron, Olivier
    Arnoult, Florence
    Ropers, Jacques
    Aegerter, Philippe
    Detaint, Delphine
    Delorme, Gabriel
    Attias, David
    Tubach, Florence
    Dupuis-Girod, Sophie
    Plauchu, Henry
    Barthelet, Martine
    Sassolas, Francois
    Pangaud, Nicolas
    Naudion, Sophie
    Thomas-Chabaneix, Julie
    Dulac, Yves
    Edouard, Thomas
    Wolf, Jean-Eric
    Faivre, Laurence
    Odent, Sylvie
    Basquin, Adeline
    Habib, Gilbert
    Collignon, Patrick
    Boileau, Catherine
    Jondeau, Guillaume
    EUROPEAN HEART JOURNAL, 2015, 36 (32) : 2160 - U37
  • [28] A double-blind, randomized, placebo-controlled laser trial methodology
    Oussedik, E.
    Saleem, M. D.
    Patel, N. U.
    Feldman, S. R.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2017, 137 (10) : B11 - B11
  • [29] A randomized, double-blind, placebo-controlled trial of pseudoephedrine in coryza
    Latte, J
    Taverner, D
    Slobodian, P
    Shakib, S
    CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2004, 31 (07): : 429 - 432
  • [30] The Efficacy and Tolerability of Milnacipran 100 mg/day Monotherapy for the Management of Fibromyalgia: A Randomized, Double-Blind, Placebo-Controlled Trial
    Arnold, Lesley M.
    Gendreau, R. Michael
    Spera, Allan
    Gendreau, Judy
    Wang, Yong
    NEUROLOGY, 2010, 74 (09) : A187 - A187