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. 2020 Apr 27;40(9):978–989. doi: 10.1177/0333102420920642

Table 2.

Anti-drug and neutralizing antibody findings across the phase 3 galcanezumab studies.

Study Study phase Placebo
n (%)
Galcanezumab
120 mg
n (%)
240 mg
n (%)
Pooled
n (%)
REGAIN Evaluable subjects DB phase 535 264 272 536
Baseline ADA present 33 (6.2) 22 (8.3) 27 (9.9) 49 (9.1)
NAb present 26 (4.9) 15 (5.7) 18 (6.6) 33 (6.2)
3-month DB treatment TE ADA+ 8 (1.5) 7 (2.7) 7 (2.6) 14 (2.6)
NAb present 3 (0.6) 6 (2.3) 4 (1.5)a 10 (1.9)
EVOLVE-1 Evaluable subjects DB phase 422 202 213 415
Baseline ADA present 25 (5.9) 18 (8.9) 23 (10.8) 41 (9.9)
NAb present 11 (2.6) 10 (5.0) 17 (8.0) 27 (6.5)
6-month DB treatment TE ADA+ 7 (1.7) 9 (4.5) 11 (5.2)a 20 (4.8)a
NAb present 6 (1.4) 9 (4.5) 11 (5.2)a 20 (4.8)a
EVOLVE-2 Evaluable subjects DB phase 443 223 214 437
Baseline ADA present 37 (8.4) 18 (8.1) 24 (11.2) 42 (9.6)
NAb present 19 (4.3) 10 (4.5) 13 (6.1) 23 (5.3)
6-month DB treatment TE ADA+ 2 (0.5) 21 (9.4)b 11 (5.1)b 32 (7.3)b
NAb present 1 (0.2) 21 (9.4)b 9 (4.2)b 30 (6.9)b
Study CGAJ Evaluable subjects OL phase 129 137 266
Baseline ADA present 8 (6.2) 12 (8.8) 20 (7.5)
NAb present 8 (6.2) 6 (4.4) 14 (5.3)
12-month OL treatment TE ADA+ 16 (12.4) 10 (7.3) 26 (9.8)
NAb present 16 (12.4) 10 (7.3) 26 (9.8)

ADA: anti-drug antibody; DB: double blind; n: number of patients within each specific category; Nab: neutralizing antibody; OL: open label; TE ADA: treatment-emergent ADA.

a

p < 0.05 versus placebo.

b

p < 0.001 versus placebo.