Investigators performed patient enrollment, monitored by an interactive voice response system. Stratified block randomization was computer-generated centrally using 8 strata and a block size of 16. Patients were stratified by previous TNF antagonist status (failure/no experience), concomitant oral corticosteroid use (yes/no), and concomitant immunosuppressive use (yes/no). Randomization schedules were generated by Takeda Pharmaceuticals International Co (Cambridge, MA), and each treatment-qualified patient received a unique randomization number used to provide

treatment assignments for dose preparation via the interactive voice response system. Saline bag covers and labels maintained blinding. Only the study learn more site pharmacist was aware of treatment assignments. Patients (at 107 sites in North America, Selleck Tenofovir Europe, Asia, Africa, and Australia) were between 18 and 80 years of age and had a diagnosis of CD with known involvement of the ileum and/or colon at 3 or more months before enrollment (Table 1). Diagnosis was based on clinical and endoscopic evidence, corroborated by results of histopathology (diagnosis occurred at ≥6 months before enrollment if a histopathology report was unavailable).

All patients had CD that was moderately to severely active, as determined by a CDAI score of 220–400 points within 7 days before enrollment, and one of the following: a screening C-reactive protein (CRP) level greater than 2.87 mg/L,25 a colonoscopy within the previous 4 months that documented ulcerations, or a fecal calprotectin level greater than 250 μg/g stool during screening in conjunction with features of active CD supported by small-bowel imaging. All patients had experienced an inadequate response, loss of response, or intolerance to TNF antagonists, immunosuppressives, all or corticosteroids within the past 5 years (Supplementary Table 1). Exclusion criteria included previous vedolizumab, natalizumab, efalizumab,

or rituximab exposure, as well as concurrent lactation or pregnancy, unstable or uncontrolled medical condition, major neurologic disorder, general anesthesia within 30 days, or planned major surgery during the study. Previous malignancies with the exception of certain cancers for which the recurrence risk after adequate treatment is expected to be low (eg, nonmetastatic basal cell and squamous cell skin cancers, cervical carcinoma in situ) resulted in exclusion, as did active drug or alcohol dependence and active psychiatric disease or other complicating factor(s) that could result in nonadherence to study procedures. The primary efficacy analysis was restricted to patients with prior TNF antagonist failure (ie, TNF antagonist–failure population, prespecified as ∼75% of enrolled patients), among whom the proportion of patients in clinical remission at week 6 was assessed (Figure 2).