The purpose of the study is to determine whether an investigational compound, ALX-0600, is safe and effective in treating Crohn's Disease.
The study is sixteen weeks in duration and there are twelve weeks of once-daily injections into your abdomen or thigh. There are a total of five visits.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
67
0.1 mg/kg injected subcutaneously daily
Advanced Clinical Therapeutics
Tucson, Arizona, United States
The percentage of subjects who are in remission (CDAI score less than 150) at week 12 of this study.
Time frame: 12 weeks after start of study
The percentage of subjects (of those who achieved response in CL0600-008) who, at week 12 of this study, maintain the response they previously achieved.
Time frame: 12 weeks after study start
The percentage of subjects who did not respond in CL0600-008 who do respond at week 12 in this study
Time frame: 12 weeks after study start
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