Phase IIa Study Evaluating AZD7798 in Crohn's Disease

Last updated: February 20, 2025
Sponsor: AstraZeneca
Overall Status: Active - Recruiting

Phase

2

Condition

N/A

Treatment

Placebo

AZD7798

Clinical Study ID

NCT06450197
D9690C00005
  • Ages 18-80
  • All Genders

Study Summary

This is a randomised, double-blind, parallel group, placebo-controlled Phase IIa study designed to evaluate the efficacy and safety of AZD7798 in participants with moderate to severe Crohn's disease.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. 18 to 80 years of age.

  2. Diagnosis of Crohn's disease established with verifiable clinical, imaging,endoscopic and/or histopathologic evidence.

  3. Moderate to severe active Crohn's disease.

  4. Ileal/ileocecal (L1), colonic (L2), or ileocolonic (L3) disease, as classified basedon the localisation of active inflammation.

  5. Capable of giving signed informed consent.

  6. A history of at least one of:

  7. Intolerance or inadequate response to conventional treatment (oralcorticosteroid, azathioprine, 6-mercaptopurine, or methotrexate), biologics, orother approved advanced therapy (eg, JAK inhibitors) OR

  8. Corticosteroid dependency (defined as inability to taper below budesonide 6mg/day or prednisolone 10 mg/day without recurrent active disease) for thetreatment of Crohn's disease.

Exclusion

Exclusion Criteria:

  1. Evidence, or clinical suspicion, of other forms of IBD or concomitant additionalactive gastrointestinal luminal inflammatory diseases.

  2. Known symptomatic strictures or bowel stenoses or strictures preventing passage ofendoscope throughout the colon.

  3. Any complications of Crohn's disease where surgery is anticipated or planned priorto end of study treatment.

  4. Evidence of extensive prior gastrointestinal surgical interventions.

  5. Within 3 months prior to screening endoscopy visit:

  6. History of toxic megacolon

  7. Diagnosis of peritonitis or need for treatment of peritonitis

  8. Bowel perforation or evidence of obstruction.

  9. Undrained fistula or abscess, including intrabdominal abscesses.

  10. Ongoing or expected nutritional dependency on total enteral or parenteral nutritionduring study.

  11. Evidence of an increased risk of colorectal cancer.

  12. Symptomatic oral Crohn's disease within one year.

  13. Any of the following treatments within the specified time period prior to screeningendoscopy visit

  14. An anti-TNF biologic within 8 weeks prior to screening endoscopy visit

  15. Any biologic targeting immune response other than an anti-TNF within 12 weeksprior to screening endoscopy visit

  16. Other advanced small molecule treatments for Crohn's disease within 4 weeksprior to screening endoscopy visit

  17. Cyclosporine, mycophenolate mofetil, sirolimus (rapamycin), thalidomide, ortacrolimus (FK-506) within 4 weeks prior to screening endoscopy visit

  18. Treatment with apheresis within 4 weeks prior to screening endoscopy visit

  19. Administration of any live vaccine within 4 weeks prior to screening endoscopyvisit to end of study

  20. Faecal microbiota transplantation within 4 weeks prior to screening endoscopyvisit

  21. Lymphocyte-depleting treatment within 12 months prior to screening endoscopyvisit

  22. Any previous exposure to AZD7798.

  23. Any changes in dosing of the following medications prior to screening endoscopyvisit as outlined:

  24. 5-aminosalicylates within 2 weeks

  25. Oral corticosteroids within 2 weeks:

(i) Prednisolone (ii) Budesonide (c) Immunomodulators within 4 weeks (d) Antibiotictherapy for the treatment of Crohn's disease (e) Probiotics within 2 weeks.

  1. Known or suspected history of chronic use of nonsteroidal anti-inflammatory drugs.

  2. Evidence of recent or currently active infection, including use of IV or oralantibiotics for documented infection within 30 days prior to screening endoscopyvisit.

  3. Evidence of chronic HBV or HCV.

  4. History of TB (active or latent) unless an appropriate course of treatment has beencompleted.

  5. Positive diagnostic TB test at screening.

  6. History of serious opportunistic infection within 12 months prior to screeningendoscopy visit.

  7. CMV colitis within previous 12 months prior to screening endoscopy visit.

  8. Positive C. difficile toxin stool test at screening.

  9. Symptomatic herpes zoster infection within 3 months prior to screening endoscopy.

  10. Any identified immunodeficiency.

  11. Abnormal laboratory results at screening suggesting participation may be unsafe,which will prevent the patient from completing the study, or will interfere with theinterpretation of the study results.

  12. Reproduction:

  13. Pregnant and breastfeeding patients, or those planning to breastfeed during thestudy

  14. FOCBP unless completely abstinent or using a highly effective contraception andbarrier method of contraception.

  15. Prolonged QTcF interval.

  16. Clinically significant cardiovascular conditions.

  17. Current malignancy or history of malignancy.

  18. Current significant major or unstable respiratory disease, heart disease,cerebrovascular disease, haematological disease, hepatic disease, renal disease,gastrointestinal disease or other major disease other than active Crohn's disease.

  19. Current enrolment in another interventional study or treatment with anyinvestigational drug within 4 months prior to screening endoscopy visit.

  20. Unstable lifestyle factors.

  21. Patients committed to an institution by virtue of an order issued either by thejudicial or the administrative authorities.

Study Design

Total Participants: 192
Treatment Group(s): 2
Primary Treatment: Placebo
Phase: 2
Study Start date:
August 28, 2024
Estimated Completion Date:
May 21, 2027

Connect with a study center

  • Research Site

    Buenos Aires, 1425
    Argentina

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  • Research Site

    Caba, C1025ABI
    Argentina

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  • Research Site

    Ciudad Autonoma de Bs As, C1013AAB
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    Ciudad Autonoma de Buenos Aires, 1128
    Argentina

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    Quilmes, B1878DVB
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    San Miguel de Tucumán, 4000
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    Adelaide, 5000
    Australia

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    Bedford Park, 5042
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    Box Hill, 3128
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    Fitzroy, 3065
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    Heidelberg, 3084
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    Liverpool, 2170
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    Melbourne, 3004
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    Parkville, 3050
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    South Brisbane, QLD 4101
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    Wollongong, 2500
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    Klagenfurt, 9020
    Austria

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    Klagenfurt am Wörthersee, 9020
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    Belgium

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    Campinas, 13092133
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    Curitiba, 80430-180
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    Jaú, 17201-130
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    Porto Alegre, 90035-903
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    Santo Andre, 09080-110
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    São José do Rio Preto, 15090-000
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    São Paulo, 04532-030
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    Gorna Oryahovitsa, 5100
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    Rijeka, 51000
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    Zagreb, 10000
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    Montpellier Cedex 5, 34090
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    Pierre Benite, 69495
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    Berlin, 14163
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    Chiba-shi, 260-8677
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    Hamamatsu-shi, 431-3192
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    Osaka-shi, 530-0011
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    Tlajomulco de Zuniga, 45645
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    Veracruz, 91900
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    Bucuresti, 011461
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    Cluj Napoca, 400380
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    Timisoara, 300002
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    Kosice, 04013
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    Nitra, 94901
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    Linköping, 58185
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    Taichung, 40447
    Taiwan

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    Taipei, 10002
    Taiwan

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    Taoyuan, 333
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    Ankara, 6500
    Turkey

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    Antalya, 07100
    Turkey

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    Bursa, 16059
    Turkey

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    Istanbul, 34890
    Turkey

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    Izmir, 35100
    Turkey

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    Malatya, 44280
    Turkey

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    İzmit, 41000
    Turkey

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    Chernivtsі, 58022
    Ukraine

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    Kiev, 02000
    Ukraine

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    Kyiv, 03680
    Ukraine

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    Ternopil, 46000
    Ukraine

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  • Research Site

    Vinnytsia, 21009
    Ukraine

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    Phoenix, Arizona 85054
    United States

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    Escondido, California 92025
    United States

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    La Jolla, California 92037
    United States

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    Hamden, Connecticut 06518
    United States

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    Orlando, Florida 32825
    United States

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    Tampa, Florida 33607
    United States

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    Idaho Falls, Idaho 83404
    United States

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    Chicago, Illinois 60611
    United States

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    Kansas City, Kansas 66160
    United States

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    Ann Arbor, Michigan 48109
    United States

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    Chesterfield, Michigan 48047
    United States

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    Clinton Township, Michigan 48038
    United States

    Active - Recruiting

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    Liberty, Missouri 64068
    United States

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    Saint Louis, Missouri 63156
    United States

    Site Not Available

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    Asheville, North Carolina 28801
    United States

    Active - Recruiting

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    Charlotte, North Carolina 28204
    United States

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    Winston-Salem, North Carolina 27103
    United States

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    Cleveland, Ohio 44195
    United States

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    Uniontown, Pennsylvania 15401
    United States

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    Dallas, Texas 75246
    United States

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    Garland, Texas 75044
    United States

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    Mansfield, Texas 76063
    United States

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    San Antonio, Texas 78229
    United States

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    Ha Noi, 100000
    Vietnam

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    Hanoi, 10000
    Vietnam

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    Ho Chi Minh, 700000
    Vietnam

    Site Not Available

  • Research Site

    Ho Chi Minh city, 700000
    Vietnam

    Site Not Available

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