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Study Evaluating AZD7798 for Treatment in Crohn's Disease Patients With an Ileostomy

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NCT06681324 · readout in 1 d

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Triple · Other
Enrollment
24actual
Sites
17
Countries
Belgium, Italy, Netherlands +4

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-12-11actualWhen the study began enrolling
Primary completion2026-08-20estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2027-09-03estimatedThe whole study's end, after follow-up
First posted2024-11-08actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Crohn's Disease

Interventions

  • Drug: AZD7798
  • Other: Placebo

Primary outcomes

what the primary-completion date above is the date OF
Number of participants with adverse events
measured from Week 0 to Week 12
Number of participants with abnormal Vital signs: Blood pressure
measured from Week 0 to Week 12
Number of participants with abnormal Vital signs: Pulse rate
measured from Week 0 to Week 12
Number of participants with abnormal values in haematology: complete blood count (CBC)
measured from Week 0 to Week 12
Number of participants with abnormal values in haematology: white blood cell (WBC) count
measured from Week 0 to Week 12
Number of participants with abnormal values in haematology: RBC
measured from Week 0 to Week 12
Number of participants with abnormal values in clinical chemistry: kidney function
measured from Week 0 to Week 12
Number of participants with abnormal values in clinical chemistry: electrolytes
measured from Week 0 to Week 12
Number of participants with abnormal values in clinical chemistry: liver function
measured from Week 0 to Week 12
Number of participants with abnormal values in clinical chemistry: hs-CRP
measured from Week 0 to Week 12
Number of participants with abnormal values in clinical chemistry: glucose
measured from Week 0 to Week 12
Number of participants with abnormal values in ECG readings
measured from Week 0 to Week 12

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