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Table 1 Demographics and clinical characteristics in all Chinese participants receiving study treatment

From: Rimegepant orally disintegrating tablet 75 mg for acute treatment of migraine in adults from China: a subgroup analysis of a double-blind, randomized, placebo-controlled, phase 3 clinical trial

Demographic

Rimegepant 75 mg

n = 538

Placebo

n = 537

Overall

N = 1075

Age, years

   

 Mean (SD)

37.3 (10.2)

36.7 (10.4)

37.0 (10.3)

 Median (range)

36 (19–71)

35 (18–70)

35 (18–71)

Sex, n (%)

   

 Female

412 (76.6)

437 (81.4)

849 (79.0)

 Male

126 (23.4)

100 (18.6)

226 (21.0)

Body mass indexa, kg/m2

   

 Mean (SD)

22.9 (3.4)

23.1 (3.4)

23.0 (3.4)

 Median (range)

22.5 (15.6–47.0)

22.8 (15.5–35.8)

22.7 (15.5–47.0)

Primary migraine type, n (%)

   

 Without aura

476 (88.5)

476 (88.6)

952 (88.6)

 With aura

62 (11.5)

61 (11.4)

123 (11.4)

Age at disease onsetb, years

   

 Mean (SD)

27.1 (9.2)

26.2 (8.6)

26.7 (8.9)

 Median (range)

27 (3–49)

26 (6–49)

26 (3–49)

Average duration of untreated attacks, hours

   

 Mean (SD)

18.0 (14.7)

18.4 (14.7)

18.2 (14.6)

 Median (range)

12 (4–72)

12 (4–72)

12 (4–72)

Number of attacks with moderate or severe pain intensity per month

   

 Mean (SD)

3.5 (1.3)

3.4 (1.2)

3.5 (1.2)

 Median (range)

3 (2–8)

3 (2–8)

3 (2–8)

Historically most bothersome symptom, n (%)

   

 Nausea

281 (52.2)

278 (51.8)

559 (52.0)

 Phonophobia

155 (28.8)

157 (29.2)

312 (29.0)

 Photophobia

102 (19.0)

101 (18.8)

203 (18.9)

 Missing

0

1 (0.2)

1 (0.1)

Took preventive migraine treatment previously, n (%)

21 (3.9)

17 (3.2)

38 (3.5)

  1. SD Standard deviation
  2. aParticipant number = 537 for rimegepant, 537 for placebo, and 1074 for overall
  3. bParticipant number = 532 for rimegepant, 532 for placebo, and 1064 for overall