Vedolizumab Induction May Prevent Celiac Enteritis

Celiac Disease Clinical Trial

Official title:

Vedolizumab Induction May Prevent Celiac Enteritis After Gluten Challenge in Established Celiac Patients in Histological Remission

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02929316
• Other study ID #: IISR-2016-101481
• Status: Terminated
• Phase: Phase 2
• Start date: June 25, 2018
• Est. completion date: October 5, 2018

Study information

• Verified date: October 2018
• Source: AGA Clinical Research Associates, LLC
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Celiac disease (CD) is characterized as an autoimmune disorder whereby gluten (a protein found in wheat, barley, rye, malt) induces an immunological response in genetically susceptible individuals. The prevalence of CD has been estimated to affect 0.5-1% of the population worldwide. Long term sequelae are numerous and include risk of lymphoma, malabsorption leading to weight loss, anemia, multiple vitamin deficiencies, osteoporosis/osteopenia, secondary autoimmunity, etc. (1)

Description:

Adult subjects with CD will be recruited through our clinic. All patients enrolled will have established CD diagnosed > 6 months. All patients will have history of abnormal MARSH score on initial duodenal biopsy at diagnosis and MARSH 0 on repeat biopsy following a gluten free diet (GFD). All patients will also have positive celiac serologies (anti-TTG, anti-gliadin, etc.) at diagnosis, as well as, positive HLA DQ2/DQ8 genetic profile. At enrollment, all patients will have negative celiac serologies, indicative of serologic remission on a gluten free diet. Female subjects of childbearing potential (does not include those with history of tubal ligation/surgical sterilization, hysterectomy and/or oophorectomy) who are sexually active with a non-sterilized male partners agree to routinely use adequate contraception from signing informed consent, during study process and for an additional 18 weeks after the last dose of vedolizumab. A male subject who is non-sterilized and sexually active with a female partner of childbearing potential agrees to use adequate contraception from signing informed consent throughout the duration of the study and for 18 weeks after the last dose.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 1
• Est. completion date: October 5, 2018
• Est. primary completion date: October 5, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Patients must meet the following criteria for study entry:

• Adult patients with Celiac Disease (CD)

• Without any additional co-morbidities

• Normal renal and hepatic function

• Diagnosis of CD established at least 6 months prior to trial with diagnostic serology, genetic profile, endoscopic appearance and histopathology report In histologic and serologic remission (defined as MARSH 0 and negative anti-tissue transglutaminase, etc.) following a gluten free diet

• Naïve to treatment with vedolizumab

• Able and willing to provide written informed consent

• Eligibility criteria for laboratory profiles - healthy patient normal laboratory reference values

• WBC 4.5-12.0 k/UL

• Platelet count- 140-415 k/UL

• Hemoglobin- 11.0-17.4 %g/dL

• Renal Function-

• Creatinine- 0.5-1.3 mg/dL

• BUN- 5-20 mg/dL

• Hepatic Function

• Albumin - 3.3-5.0 g/dL

• INR- 0.9-1.1

• AST- 0-37 U/L

• ALT- 0-40 U/L

• Total Bilirubin- 0.1-1.3 mg/dL

• Alk Phos- 35-150 U/L

Exclusion Criteria:

• Patients who meet any of the following criteria will be excluded from study entry:

• Abnormal MARSH score on enrollment histopathology

• Elevated celiac serologies (anti-tissue transglutaminase, etc.)

• Current use of biologics or immunomodulators Adalimumab, infliximab, Ustekinumab, Golimumab, Tocilizumab, Certolizumab, Etanercept, Rituximab, Anakinra, Abatacept, Tofacitinib, Methotrexate, Azathioprine, 6-MP.

• Current use of immunosuppressive therapy including intermittent systemic corticosteroids within two months of vedolizumab induction

• History of intestinal lymphoma (MALToma, etc.)

• History of cancer including hematologic malignancy, solid tumors, carcinoma in situ, etc.

• Pregnant or lactating

• Fertile females will require at least one form of birth control

• Lack of peripheral venous access

• Inability to comply with study protocol, in the opinion of the investigator

• Neurological conditions which may interfere with monitoring for PML

• History of demyelinating disease or history of major neurological disease

• History of alcohol, drug or chemical abuse < 6 months prior to screening

• History of active tuberculosis (TB) or a positive screening test for latent mycobacterium tuberculosis infection

• Positive PPD= > 10 mm or > 5mm in patients on 15 mg or more of prednisone

• History of BCG vaccination should be screened using Quantiferon TB Gold test

• An Indeterminate Quantiferon test will require a chest X-ray to rule out active TB and consultation with an infectious disease specialist to confirm the risk of latent

• TB is low and that patients can be safely enrolled in the trial

• History of recurrent opportunistic infections and/or of severe or disseminated viral infections

• Active autoimmune disease

• Active inflammatory bowel disease

Related Conditions & MeSH terms

• Celiac Disease
• Enteritis

Intervention

Drug:
• Vedolizumab
IV infusion week 0, 2 and 6

Locations

Country	Name	City	State
United States	AGA Clinical Research Associates, LLC	Egg Harbor Township	New Jersey
United States	Theresa Stevens	Egg Harbor Township	New Jersey

Sponsors (2)

Lead Sponsor	Collaborator
AGA Clinical Research Associates, LLC	Takeda

Country where clinical trial is conducted

United States, 

References & Publications (9)

Green PH, Cellier C. Celiac disease. N Engl J Med. 2007 Oct 25;357(17):1731-43. Review. — View Citation

Kelly CP, Green PH, Murray JA, Dimarino A, Colatrella A, Leffler DA, Alexander T, Arsenescu R, Leon F, Jiang JG, Arterburn LA, Paterson BM, Fedorak RN; Larazotide Acetate Celiac Disease Study Group. Larazotide acetate in patients with coeliac disease unde — View Citation

Lee SK, Lo W, Memeo L, Rotterdam H, Green PH. Duodenal histology in patients with celiac disease after treatment with a gluten-free diet. Gastrointest Endosc. 2003 Feb;57(2):187-91. — View Citation

Leffler D, Schuppan D, Pallav K, Najarian R, Goldsmith JD, Hansen J, Kabbani T, Dennis M, Kelly CP. Kinetics of the histological, serological and symptomatic responses to gluten challenge in adults with coeliac disease. Gut. 2013 Jul;62(7):996-1004. doi: — View Citation

Leffler DA, Kelly CP, Abdallah HZ, Colatrella AM, Harris LA, Leon F, Arterburn LA, Paterson BM, Lan ZH, Murray JA. A randomized, double-blind study of larazotide acetate to prevent the activation of celiac disease during gluten challenge. Am J Gastroenter — View Citation

Leffler DA, Schuppan D. Update on serologic testing in celiac disease. Am J Gastroenterol. 2010 Dec;105(12):2520-4. doi: 10.1038/ajg.2010.276. Review. — View Citation

Lionetti E, Castellaneta S, Francavilla R, Pulvirenti A, Tonutti E, Amarri S, Barbato M, Barbera C, Barera G, Bellantoni A, Castellano E, Guariso G, Limongelli MG, Pellegrino S, Polloni C, Ughi C, Zuin G, Fasano A, Catassi C; SIGENP (Italian Society of Pe — View Citation

Vahedi K, Mascart F, Mary JY, Laberenne JE, Bouhnik Y, Morin MC, Ocmant A, Velly C, Colombel JF, Matuchansky C. Reliability of antitransglutaminase antibodies as predictors of gluten-free diet compliance in adult celiac disease. Am J Gastroenterol. 2003 M — View Citation

Wahab PJ, Meijer JW, Mulder CJ. Histologic follow-up of people with celiac disease on a gluten-free diet: slow and incomplete recovery. Am J Clin Pathol. 2002 Sep;118(3):459-63. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Normal histopathology following induction dosing with vedolizumab	Remission is defined in this study of negative celiac antibodies and normal duodenal biopsies	12 weeks
Primary	Normal histopathology following induction dosing with vedolizumab after 2 week gluten challange	Remission is defined in this study as negative celiac antibodies and normal duodenal biopsies	12 weeks