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. 2017 Dec 15;68(1):40–48. doi: 10.1136/gutjnl-2017-314562

Table 2.

Patient disposition in the open-label extension study

PF-04236921
Enrolled and treated* 191
 Responder at entry 89
 Non-responder at entry 99
 Responder status missing at entry 3
End of treatment: completed 69
 Baseline HBI data 65
 Responders 36
 Non-responders 29
End of treatment: discontinued 122
 Baseline HBI data 121
 Responders 51
 Non-responders 70
End of study (includes follow-up period): completed 111
Analysed for safety 191
Analysed for efficacy 189†

*Patients in the prior induction study achieving CDAI-70 (proportion of patients who achieved a ≥70-point reduction in Crohn’s Disease Activity Index (CDAI) score) response were considered responders at entry and those patients not achieving CDAI-70 response were considered non-responders at entry.

†Patients who received at least one dose of PF-04236921 in this study but excludes two patients with a quality issue.

HBI, Harvey-Bradshaw Index.