Subgroup | No draining fistulas* | |
Week 26 % of patients | Week 56 % of patients | |
No baseline immunosuppressant use | ||
Placebo (n = 21) | 19 | 19 |
Both adalimumab groups (n = 39) | 33 (p = 0.369) | 36 (p = 0.241) |
Baseline immunosuppressant use | ||
Placebo (n = 26) | 8 | 8 |
Both adalimumab groups (n = 31) | 26 (p = 0.092) | 29 (p = 0.051) |
No baseline CD-related antibiotic use | ||
Placebo (n = 28) | 14 | 14 |
Both adalimumab groups (n = 44) | 32 (p = 0.162) | 36 (p = 0.059) |
Baseline CD-related antibiotic use | ||
Placebo (n = 19) | 11 | 11 |
Both adalimumab groups (n = 26) | 27 (p = 0.264) | 27 (p = 0.264) |
*Patients who had no draining fistulas at the last two post-baseline evaluations in the double-blind period on or before the week 26 or week 56 visits were classified as no; otherwise, patients were classified as yes. p Values from χ2 tests comparing both adalimumab groups combined versus placebo. CD, Crohn’s disease.