Table 1.
Study | Year | Group (dose, mg) | No. | Female/Male | Age, yr | Outcome measures |
01657370[13] | 2012 | Ub = 1 | 28 | 26/2 | NA | ①②③④⑤ |
Ub = 10 | 26 | 22/4 | ||||
Ub = 25 | 28 | 23/5 | ||||
Ub = 50 | 28 | 26/2 | ||||
Ub = 100 | 27 | 18/9 | ||||
Placebo | 28 | 25/3 | ||||
voss2016[14] | 2012 | Ub = 1 | 138 | 95/12 | 39.6 ± 10.7 | ①②③④⑤ |
Ub = 10 | 139 | 92/16 | 41.1 ± 10.9 | |||
Ub = 25 | 139 | 91/13 | 41.4 ± 11.5 | |||
Ub = 50 | 139 | 92/14 | 40.7 ± 12.3 | |||
Ub = 100 | 139 | 90/12 | 41.9 ± 11.0 | |||
Placebo | 139 | 99/14 | 40.8 ± 11.4 | |||
Lipton2019[15] | 2018 | Ub = 25 | 561 | 501/60 | 41.6 ± 12.3 | ①②③④⑤ |
Ub = 50 | 562 | 497/65 | 41.0 ± 12.4 | |||
Placebo | 563 | 494/69 | 41.5 ± 12.2 | |||
Dodick2019[16] | 2017 | Ub = 50 | 556 | 493/63 | 40.2 ± 12.0 | ①②③④⑤ |
Ub = 100 | 557 | 479/78 | 40.7 ± 12.4 | |||
Placebo | 559 | 491/68 | 40.5 ± 12.2 | |||
Goadsby2019[17] | 2018 | Ub = 100 | 260 | 140/116 | NA | ①②③④⑤ |
Placebo | 256 | 141/119 |
NA = not available, Ub = ubrogepant; ① percentage of participants reporting pain relief at 2 h postdose; ② percentage of participant reporting absence of photophobia at 2 h postdose; ③ percentage of participants reporting absence of nausea at 2 h postdose; ④ percentage of participants reporting absence of phonophobia at 2 h postdose; ⑤ common adverse effects.