Table 2.
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.