Skip to main content

Table 2 Primary endpoint: mean worst EAPP and absolute change from baseline to end of intervention (measured daily on the NRS as ESD item 1)—primary per-protocol set

From: Efficacy and safety of eliapixant in endometriosis-associated pelvic pain: the randomized, placebo-controlled phase 2b SCHUMANN study

Timepoint

 

Eliapixant 25 mg BID

Eliapixant 75 mg BID

Eliapixant

150 mg BID

Placebo

Total

Baseline

n

31

31

31

30

123

 

Missing

0

0

0

0

0

 

Mean (SD)

6.40 (1.66)

6.13 (1.77)

6.95 (1.38)

6.14 (1.96)

6.41 (1.72)

 

Median

6.68

6.25

6.96

5.74

6.62

 

Q1, Q3

5.27, 7.44

4.86, 7.46

6.19, 7.86

4.56, 7.64

5.12, 7.58

 

Min, max

3.1, 9.6

3.0, 9.6

3.8, 9.9

2.6, 10.0

2.6, 10.0

Week 12 (EOI)

n

24

22

20

26

92

 

Missing

7

9

11

4

31

 

Mean (SD)

4.57 (2.10)

4.15 (2.49)

5.15 (2.42)

4.29 (1.71)

4.52 (2.17)

 

Median

4.61

3.91

4.86

3.95

4.18

 

Q1, Q3

3.15, 5.99

1.61, 6.54

3.30, 7.13

3.08, 5.80

3.09, 6.13

 

Min, max

0.5, 8.5

0.6, 8.6

0.5, 10.0

1.5, 8.3

0.5, 10.0

Change from baseline

n

24

22

20

26

92

 

Missing

7

9

11

4

31

 

Mean (SD)

–1.56 (1.35)

–2.12 (2.66)

–1.88 (2.03)

–1.89 (1.91)

–1.86 (2.00)

 

Median

–1.36

–1.39

–1.30

–1.67

–1.40

 

Q1, Q3

–2.13, − 0.50

–3.29, − 0.17

–3.46, − 0.19

–3.04, − 0.39

–3.01, − 0.35

 

Min, max

–4.1, 0.4

–7.9, 1.9

–6.2, 1.6

–6.3, 1.3

–7.9, 1.9

  1. Abbreviations: BID twice daily, EAPP endometriosis-associated pelvic pain (item 1 in the Endometriosis Symptom Diary [ESD]), EOI end of intervention, NRS numeric rating scale, Q1 first quartile, Q3 third quartile, SD standard deviation