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. 2020 Nov 16;23(1):3. doi: 10.1208/s12248-020-00518-0

Table VI.

Infusion-Related Reactions and Immunogenicity Status of Patients During Vedolizumab Maintenance in GEMINI 1 and GEMINI 2 Using ELISA

AEs defined by the investigator as infusion-related reactions (yes/no), n (%) Maintenance study ITTa Non-ITT Combined
Placebob (from week 6) Vedolizumab Q8W Vedolizumab Q4W Placeboc (from week 0) Vedolizumab Q4W (week 6 nonresponders) Continuous vedolizumabd
N = 279 N = 276 N = 279 N = 296 N = 879 N = 1434
Yes 8 12 18 9 31 61
  ADA negative 7 (88) 11 (92) 18 (100) 9 (100) 29 (94) 58 (95)
  ADA positive 1 (13) 1 (8) 0 0 2 (6) 3 (5)
    Transiently positive 0 0 0 0 0 0
    Persistently positive 1 1 0 0 2 3
    Any neutralizing ADA positivee 0 0 0 0 2 2
No 271 264 261 287 848 1373
  ADA negative 227 (84) 257 (97) 258 (99) 279 (97) 805 (95) 1320 (96)
  ADA positive 44 (16) 7 (3) 3 (1) 8 (3) 43 (5) 53 (4)
    Transiently positive 14 6 3 3 38 47
    Persistently positive 30 1 0 5 5 6
    Any neutralizing ADA positivee 24 4 3 4 24 31

Not all patients had evaluable samples. N = total number of patients with samples tested in each treatment group. Proportions are based on nonmissing values

AE adverse event, ADA vedolizumab anti-drug antibody, ELISA enzyme-linked immunosorbent assay, ITT intent to treat, Q4W every 4 weeks, Q8W every 8 weeks

aPatients who were responders to vedolizumab induction at week 6 and were randomized into the maintenance-phase ITT population

bPatients who received vedolizumab during induction and were randomized to placebo at the maintenance phase

cPatients who were randomized to placebo at both the induction and maintenance phases

dAll patients who received induction and maintenance vedolizumab, including week 6 responders who were randomized to vedolizumab in the maintenance phase plus patients who did not respond at week 6 and received maintenance vedolizumab Q4W

eSamples positive for neutralizing ADA with no reportable titer were considered missing (i.e., no detectable positive neutralizing ADA was present in the sample)