About this trial
The choice of drug therapy for Crohn's disease depends on several factors, such as the severity of the condition, the sections of the bowel affected, or the patient's previous treatment history. Conventional therapy consists of a short course of corticosteroid treatment followed by azathioprine therapy. Alternatively, there are so-called advanced therapies using biologics (biotechnologically produced protein substances such as antibodies), for example mirikizumab. This study aims to investigate whether direct, early treatment with mirikizumab is more effective than the standard therapy of azathioprine in combination with corticosteroids. Following an inclusion phase, patients will be randomly assigned to either treatment with mirikizumab or azathioprine + corticosteroids. Patients in the azathioprine arm may switch to mirikizumab therapy at three time points from week 24 onwards if they do not respond adequately to azathioprine therapy. The study consists of an initial treatment period of 12 weeks (induction therapy) and a maintenance therapy period of 40 weeks. Patients in the mirikizumab arm receive 13 doses of mirikizumab. This includes initially 900 mg intravenously every 4 weeks followed by 300 mg subcutaneously. In the azathioprine arm patients receive daily administration of azathioprine tablets in combination with a steroid. Assignment to one of the two treatment options is randomised with equal probability for each of the treatment options.
Eligibility criteria
Qualifiers
Given written informed consent prior to any study-specific procedures.
Willing and able to complete the scheduled study assessments, including ileocolonoscopy and daily Diary entry.
Willing to comply with contraception requirements (as specified in Section 7.7 Contraception requirements).
Age 18-75 years.
Disqualifiers
Acute severe/fulminant Crohn's disease requiring immediate inpatient management or urgent surgery at screening (e.g., obstructive complication with imminent surgery, perforation, draining fistula, uncontrolled sepsis/abscess, toxic megacolon).
Oral and rectal 5-ASA or rectal steroids treatment within 2 weeks prior to screening colonoscopy.
History of malignancy, except for non-melanoma skin cancer that has been successfully treated and considered cured at screening.
Planned or foreseeable surgery at or before randomization (Week 0).
Trial design
Treatments tested in this trial
- Mirikizumab
- Azathioprine (AZA)