Study Evaluating AZD7798 for Treatment in Crohn's Disease Patients With an Ileostomy
- Registration Number
- NCT06681324
- Lead Sponsor
- AstraZeneca
- Brief Summary
The purpose of this study is to evaluate safety, tolerability, and effect on mucosal repair of AZD7798 compared with placebo in participants with active ileal Crohn's disease and an ileostomy.
- Detailed Description
This is a participant-and investigator-blind, randomized, parallel-group, placebo controlled phase II study designed to evaluate safety, tolerability, and mucosal repair with AZD7798 in participants with active ileal Crohn's disease and an ileostomy. This study will include a screening period, an induction period, an open-label maintenance period, and a follow-up period. Approximately 30 participants will be randomized globally to receive either AZD7798 or placebo during 12-week participant- and investigator- blind induction period. At week 12 after induction period, all eligible participants will enter 40-week open label maintenance period. Follow-up visits will take place 8 weeks and 18 weeks after the last dose of study intervention, whether this occurs during the induction period or the open-label maintenance period.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 30
- 18 to 80 years of age.
- Diagnosis of Crohn's disease established with clinical, imaging, endoscopic, and/or histopathologic evidence.
- Ileostomy for at least 3 months.
- Prior to screening endoscopy, clinical suspicion of active ileal inflammation based on at least one of the following: previous endoscopy, imaging (CT, MRI, IUS), or FCP above upper reference limit.
- Active ileal Crohn's disease as determined by active intestinal mucosal inflammation, as demonstrated on video recorded ileoscopy performed during the screening period and scored by a blinded central reader with agreement on the SES CD ≥ 4 of the ileal segment proximal to the stoma. Participants with inflammation in additional intestinal segments are not excluded.
- Capable of giving signed informed consent.
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Concomitant additional gastrointestinal luminal inflammatory diseases
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Strictures/stenoses preventing passage of endoscope throughout the specified segment
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Short bowel syndrome
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Within 3 months prior to screening:
- Diagnosis of peritonitis or need treatment of peritonitis
- Bowel perforation or evidence of obstruction
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All intrabdominal, cutaneous and perianal/perirectal abscesses and fistulae are excluded with exception of: cutaneous and perianal/perirectal abscesses which are adequately drained 4 weeks prior to randomization, and intraabdominal fistulae between bowel segments only without complications
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Ongoing or expected nutritional dependency on total enteral or parenteral nutrition during study (partial nutrition acceptable).
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In participants with any remaining colon and/or rectum, evidence of an increased risk of colorectal cancer, including:
- Adenomatous colonic/rectal polyps that have not been removed
- Intestinal dysplasia
- Not undertaking appropriate surveillance, if indicated, for colorectal dysplasia/malignancy
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Reversal of ileostomy or formation of J-pouch planned prior to end of study period.
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High-output stoma (eg, > 2000 mL/24 hours) associated with volume depletion and/or electrolyte disturbance to the extent that, in the opinion of the Investigator, it may put the participant at undue risk because of participation in the study, or impact their ability to participate in the study or interfere with the interpretation of study data.
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Any of the following treatments within the specified time period:
- An anti-TNF biologic within 8 weeks prior to randomization
- Any biologic targeting immune response other than an anti-TNF (including vedolizumab and ustekinumab) within 12 weeks prior to randomization.
- Other advanced small molecule treatments for Crohn's disease within 4 weeks prior to randomization
- Cyclosporine, mycophenolate mofetil, sirolimus (rapamycin), thalidomide, or tacrolimus within 4 weeks prior to randomization
- Treatment with apheresis (eg, Adacolumn, Cellsorba) within 4 weeks prior to randomization
- Administration of any live vaccine within 4 weeks prior to randomization, or planned administration of any such vaccine during the study
- Faecal microbiota transplantation within 4 weeks prior to randomization
- Regular intake of NSAIDs within 12 weeks prior to screening ileoscopy and during the study (defined as at least times per week for more than 3 months; not applicable to daily aspirin use up to 325 mg per day)
- Lymphocyte-depleting treatment, including, but not limited to rituximab, within 12 months prior to randomization
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Any changes in dosing of the following medications prior to screening ileoscopy as outlined
- 5-aminosalicylates within 2 weeks
- Oral corticosteroids within 2 weeks. Also excluded if on stable dosing of steroids exceeding the following dose equivalents:
(i) Systemic steroids > 20 mg/day prednisolone dose or equivalent (ii) Locally targeted steroids exceeding maximum budesonide dose or equivalent [9 mg/day] (c) Immunomodulators (thiopurines or methotrexate) within 4 weeks (d) Antibiotic therapy for the treatment of Crohn's disease, eg, ciprofloxacin or metronidazole within 2 weeks (e) Probiotics within 2 weeks
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Evidence of recent or currently active infection, including use of IV or oral antibiotics for documented infection within 30 days prior to screening.
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Evidence of chronic hepatitis B or C infection
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History of TB (active or latent) unless an appropriate course of treatment has been completed.
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Positive diagnostic TB test at screening.
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History of serious opportunistic infection within 12 months prior to screening
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Symptomatic herpes zoster infection within 3 months prior to screening.
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Positive C. difficile toxin test at screening.
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Any identified immunodeficiency
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Any other abnormal laboratory results at screening, which, in the opinion of the Investigator, will prevent the participant from completing the study or will interfere with the interpretation of the study results
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Prolonged QTcF interval > 450 ms (or > 480 ms for patients with bundle branch block) or congenital long-QT syndrome or family history of long-QT syndrome or sudden cardiac death in age < 40 years.
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Clinically significant cardiovascular conditions
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Reproduction:
- Pregnant and breastfeeding participants, or those planning to breastfeed during the study
- FOCBP, unless they agree to complete abstinence or to use a highly effective contraceptive method AND barrier method
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Current malignancy or history of malignancy
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Current significant major or unstable respiratory disease, heart disease, cerebrovascular disease, haematological disease, hepatic disease including large duct primary sclerosing cholangitis with jaundice, recurrent cholangitis or cirrhosis, renal disease, gastrointestinal disease, or other major disease other than active Crohn's disease.
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Current enrolment in another interventional study or treatment with any investigational drug within 4 months (or 5 half-lives, whichever is longer) prior to screening
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Unstable lifestyle factors
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Participants committed to an institution by virtue of an order issued either by the judicial or the administrative authorities.
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Involvement in the planning and/or conduct of the study
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Judgement by the Investigator that the participant should not participate in the study if the participant is unlikely to comply with study procedures, restrictions, and requirements.
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Previous randomization in the present study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description AZD7798 AZD7798 AZD7798 Placebo Placebo Placebo
- Primary Outcome Measures
Name Time Method Number of participants with adverse events from Week 0 to Week 12 Summary of any adverse events and also by MedDRA SOC and Preferred term
Number of participants with abnormal values in haematology: complete blood count (CBC) from Week 0 to Week 12 The variables platelet count, red blood cell (RBC) count, haemoglobin, haematocrit will be summarized with descriptive statistics
Number of participants with abnormal values in haematology: white blood cell (WBC) count from Week 0 to Week 12 The variables neutrophils, lymphocytes, monocytes, eosinophils, and basophils will be summarized with descriptive statistics
Number of participants with abnormal values in haematology: RBC from Week 0 to Week 12 The variables mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH) and percentage of reticulocytes will be summarized with descriptive statistics
Number of participants with abnormal Vital signs: Blood pressure from Week 0 to Week 12 Systolic and diastolic blood pressure will be summarized by descriptive statistics
Number of participants with abnormal Vital signs: Pulse rate from Week 0 to Week 12 Pulse rate will be summarized by descriptive statistics
Number of participants with abnormal values in clinical chemistry: kidney function from Week 0 to Week 12 The variables creatinine and blood urea nitrogen (BUN) will be summarized with descriptive statistics
Number of participants with abnormal values in clinical chemistry: electrolytes from Week 0 to Week 12 The variables potassium, sodium, and calcium will be summarized with descriptive statistics
Number of participants with abnormal values in clinical chemistry: liver function from Week 0 to Week 12 The variables ALT (Alanine Aminotransferase), AST (Aspartate Aminotransferase), and ALP (alkaline phosphatase), and albumin will be summarized with descriptive statistics
Number of participants with abnormal values in clinical chemistry: hs-CRP from Week 0 to Week 12 The variable hs-C-reactive protein will be summarized with descriptive statistics
Number of participants with abnormal values in clinical chemistry: glucose from Week 0 to Week 12 The variable glucose will be summarized with descriptive statistics
Number of participants with abnormal values in ECG readings from Week 0 to Week 12 12-lead ECGs will be obtained using an ECG machine, that automatically measures RR/HR, PR, QRS, QT and Corrected QT (QTc) intervals, and summarized with descriptive statistics
- Secondary Outcome Measures
Name Time Method Difference in mean change from baseline in endoscopic score between active and placebo Week 12 Simple Endoscopic Score for Crohn's Disease (SES-CD) is based on the evaluation of ileum, and the presence and size of ulcerations and the extent of the inflammatory area and stenosis are assessed. The segment is scored from 0 to 12, higher scores indicating more active disease
Number of participants with endoscopic response Week 12 Endoscopic response is defined as ≥ 50% decrease from baseline in SES-CD total score and based on the evaluation of ileum and the presence and size of ulcerations and the extent of the inflammatory area and stenosis are assessed. The segment is scored from 0 to 12, higher scores indicating more active disease
Number of participants with endoscopic remission Week 12 Endoscopic remission is defined as SES-CD total score \< 4 and at least 2 point reduction from baseline with no sub score \> 1 in any individual variable. SES-CD is based on the evaluation of ileum, and the presence and size of ulcerations and the extent of the inflammatory area and stenosis are assessed. The segment is scored from 0 to 12, higher scores indicating more active disease
Serum AZD7798 concentration up to 52 Weeks Serum AZD7798 concentration (PK)
Incidence of anti-drug antibody response up to 52 Weeks Incidence of anti-drug antibody (ADA) response - number and percentages with a positive ADA result
Titre of anti-drug antibody response up to 52 Weeks Titre of anti-drug antibody (ADA) response - immunogenicity titre will be summarized descriptively as a continuous variable, only for ADA positive tests
Number of participants with adverse events in active treatment from Week 12 to Week 52 Summary of any adverse events and also by MedDRA SOC and Preferred term
Number of participants with abnormal vital signs: Blood pressure from Week 12 to Week 52 Systolic and diastolic blood pressure will be summarized by descriptive statistics
Number of participants with abnormal vital signs: Pulse rate from Week 12 to Week 52 Pulse rate will be summarized by descriptive statistics
Number of participants with abnormal values in haematology: complete blood count (CBC) from Week 12 to Week 52 The variables platelet count, red blood cell (RBC) count, haemoglobin, haematocrit will be summarized with descriptive statistics
Number of participants with abnormal values in haematology: white blood cell (WBC) count from Week 12 to Week 52 The variables neutrophils, lymphocytes, monocytes, eosinophils, and basophils will be summarized with descriptive statistics
Number of participants with abnormal values in haematology: RBC from Week 12 to Week 52 The variables mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH) and percentage of reticulocytes will be summarized with descriptive statistics
Number of participants with abnormal values in clinical chemistry: kidney function from week 12 to week 52 The variables creatinine and blood urea nitrogen (BUN) will be summarized with descriptive statistics
Number of participants with abnormal values in clinical chemistry: electrolytes from Week 12 to Week 52 The variables potassium, sodium, and calcium will be summarized with descriptive statistics
Number of participants with abnormal values in clinical chemistry: liver function from Week 12 to Week 52 The variables ALT (Alanine Aminotransferase), AST (Aspartate Aminotransferase), and ALP (alkaline phosphatase), and albumin will be summarized with descriptive statistics
Number of participants with abnormal values in clinical chemistry: hs-CRP from Week 12 to Week 52 The variable hs-C-reactive protein will be summarized with descriptive statistics
Number of participants with abnormal values in clinical chemistry: glucose from Week 12 to Week 52 The variable glucose will be summarized with descriptive statistics
Number of participants with abnormal values in ECG readings from week 12 to week 52 12-lead ECGs will be obtained using an ECG machine, that automatically measures RR/HR, PR, QRS, QT and Corrected QT (QTc) intervals, and summarized with descriptive statistics
Trial Locations
- Locations (1)
Research Site
🇬🇧London, United Kingdom