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. 2016 May 25;6(2):111–124. doi: 10.1007/s13555-016-0121-x

Table 2.

Primary and secondary end points at week 12 for brodalumab compared to placebo and ustekinumab

Disclaimer: these data were tabulated from independent studies that were not conducted in a head-to-head manner

End point Study Brodalumab 210 mg Brodalumab 140 mg Placebo Ustekinumab 45 mg or 90 mg
PASI 75 AMAGINE-1, % (no./total), 95% CI 83.3% (185/222), 78–88 60.3% (132/219), 54–67 2.7% (6/220), 1–6
AMAGINE-2, % (no./total), 95% CI 86.3%†, ¶ (528/612), 83–89 66.6%†, ¶ (406/610), 63–70 8.1% (25/309), 5–12 70% (210/300), 65–75
AMAGINE-3, % (no./total), 95% CI 85.1%†, * (531/624), 82–88 69.2%†, ¶ (396/629), 65–73 6% (19/315), (4–9 69.3% (217/313), 64–74
PASI 90 AMAGINE-1, % (no./total), 95% CI 70.3% (156/222), 64–76 42.5% (93/219), 36–49 0.9% (2/220), 0–3
AMAGINE-2, % (no./total), 95% CI 69.9%†, * (428/612), N/A 49.0%†, ¶ (299/610), N/A 1.9% (6/309), N/A 47.0% (141/300), N/A
AMAGINE-3, % (no./total), 95% CI 68.9%†, * (430/624), N/A 52.0%†, ¶ (327/629), N/A 2.9% (9/315), N/A 47.9% (150/313), N/A
PASI 100 AMAGINE-1, % (no./total), 95% CI 41.9% (93/222), 36–49 23.3% (51/219), 18–30 0.5% (1/220), 0–3
AMAGINE-2, % (no./total), 95% CI 44.4%†, * (272/612), 41–49 25.7%†, ¶ (157/610), 22–29 0.6% (2/309), 0–2 21.7% (65/300), 17–27
AMAGINE-3, % (no./total), 95% CI 36.7%†, * (229/624), 33–41 27%†, * (170/629), 24–31 0.3% (1/315), 0–2 18.5% (58/313), 14–23
sPGA 0/1 AMAGINE-1, % (no./total), 95% CI 75.7% (168/222), 70–81 53.9% (118/219), 47–61 1.4% (3/220), 0–4
AMAGINE-2, % (no./total), 95% CI 78.6%†, * (481/612), 75–82 58.0%†, ¶ (354/610), 54–62 4% (12/309), 2–7 61% (183/300), 55–67
AMAGINE-3, % (no./total), 95% CI 79.6%†, * (497/624), 76–83 59.9%†, ¶ (377/629), 56–64 4.1% (13/315), 2–7 57.2% (179/313), 52–63
PSI Response AMAGINE-1, % (no./total), 95% CI 60.8% (135/222), 54–67 53.0% (116/219), 46–60 4.1% (9/220), 2–8
AMAGINE-2, % (no./total), 95% CI 67.6% (414/612), 64–71 51.5%a (314/610), 47–56 6.8% (21/309), 4– 0 55.3% (166/300), 50–61
AMAGINE-3, % (no./total), 95% CI 61.2% (382/624), 57–65 53.4% (336/629), 49–57 6.3% (17/315), 4–10 51.8% (162/313), 46–57

sPGA static Physician Global Assessment, PASI Psoriasis Area and Severity Index, PSI Psoriasis Symptom Inventory, CI confidence interval

* P < 0.01 for the comparison with ustekinumab

P < 0.001 for the comparison with placebo

P > 0.05 for the comparison with ustekinumab