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Completed

NCT Number: NCT02637141

A Study to Evaluate the Efficacy and Safety of AMG 714 in Adult Patients With Celiac Disease

This study is designed to evaluate the efficacy and safety of AMG 714 for the attenuation of the effects of gluten exposure in adult patients with celiac disease during a gluten challenge.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

ODL, Oulu, Finland

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of celiac disease by intestinal biopsy at least 12 months prior to screening
  • On a gluten-free diet for at least 12 months
  • Negative celiac serology
  • Avoidance of pregnancy

Exclusion criteria

  • Severe complications of celiac disease, such as refractory celiac disease
  • Celiac symptoms
  • Other concomitant autoimmune disease
  • Chronic, active gastrointestinal disease
  • Infections, concomitant diseases
  • Prohibited medications

Treatment and study plan

AMG 714

Biological

AMG 714 administered by subcutaneous injection

Other names: PRV-015

Placebo

Biological

Matching placebo to AMG 714 administered by subcutaneous injection

Placebo Gluten Challenge

Other

Gluten-free cookies (Finnish rusks)

Gluten Challenge

Other

Gluten-containing cookies (Finnish rusks), 1-2 g gluten per serving

Primary outcomes

  1. Percent Change From Baseline in Villous Height to Crypt Depth Ratio (VH:CD) at Week 12

    Time frame: Baseline and week 12

    Attenuation of the effects of gluten exposure was assessed by measuring the percent change from baseline in villous height to crypt depth ratio after 10 weeks of gluten challenge.

    Villi are the small fingerlike projections that line the small intestine and promote nutrient absorption and are often shortened in patients with celiac disease. Crypts are grooves between the villi that are often elongated in patients with celiac disease. A decreased VH:CD ratio indicates worsening disease.

    Small bowel biopsies were performed at baseline and week 12; histological assessments were performed by a blinded central pathologist.

Secondary outcomes

  1. Percent Change From Baseline in Intraepithelial Lymphocyte Density at Week 12

    Time frame: Baseline and week 12

    Intraepithelial lymphocytes (IELS) are white blood cells interspersed between epithelial cells of the small and large intestine where they function to preserve the integrity of the mucosal barrier by protecting the epithelium against pathogen or immune-induced pathology. Increased intraepithelial lymphocytes is associated with celiac disease.

    Small bowel biopsies were performed at baseline and week 12; histological assessments were performed by a blinded central pathologist.

  2. Number of Participants With Improvement in Marsh Score at Week 12

    Time frame: Baseline and week 12

    The Marsh classification system describes the stages of damage in the small intestine as seen under a microscope, with possible values of 0, 1, 2, 3a, 3b, or 3c. A score of 0 (best score) indicates that the intestinal lining is normal and celiac disease highly unlikely, a score of 3c (worst score) indicates increased intraepithelial lymphocytes, increased crypt hyperplasia and complete villi atrophy. Improvement is defined as a lower grade on the Marsh score scale compared to baseline.

  3. Percent Change From Baseline in Anti-Tissue Transglutaminase (tTG) Immunoglobulin A (IgA) Antibodies at Week 12

    Time frame: Baseline and week 12

    Levels of anti-tTG IgA antibodies in serum were determined using an enzyme-linked immunosorbent assay (ELISA) immunoassay.

  4. Change From Baseline in Anti-Deamidated Gliadin Peptide (DGP) Antibodies at Week 12

    Time frame: Baseline and week 12

    Levels of serum anti-DGP antibodies (immunoglobulin A [IgA] and immunoglobulin G [IgG]) were determined using ELISA immunoassay.

  5. Number of Weekly Bowel Movements at Baseline and Week 12

    Time frame: Baseline and week 12

    Participants were asked to record every bowel movement during the study using an electronic diary. If no bowel movements were experienced on any given day, the participant was required to document this using the electronic diary.

  6. Number of Participants With Diarrhoea at Baseline and Week 12

    Time frame: Baseline and week 12

    The Bristol Stool Form Scale (BSFS) is a pictorial aid to help study participants identify the shape and consistency of their bowel movements. Participants were asked to complete this form daily using an electronic diary at the time of each bowel movement. The BSFS categorizes bowel movements into 7 types, from Type 1 (separate hard lumps, like nuts; hard to pass) to Type 7 (watery, no solid pieces, entirely liquid).

    Diarrhoea was defined as at least one BSFS score >= 6 for the given week.

  7. Percent Change From Baseline in Total Weekly Gastrointestinal Symptom Rating Scale (GSRS) Score at Week 12

    Time frame: Baseline and 12 weeks

    The GSRS is a 15-question 7-scale questionnaire used to assess 5 dimensions of gastrointestinal syndromes: diarrhea, indigestion, constipation, abdominal pain, and reflux. Questions are scored between 1 (no discomfort at all) and 7 (very severe discomfort). The total GSRS score is calculated as the sum of the scores of all 15 questions, and ranges from 15 (no discomfort at all) to 105 (very severe discomfort in all 5 dimensions of gastrointestinal syndromes).

  8. Change From Baseline in Total Celiac Disease GSRS (CeD-GSRS) Score at Week 12

    Time frame: Baseline and 12 weeks

    The CeD-GSRS score is derived from a subset of questions from the GSRS questionnaire, including the diarrhea, indigestion, and abdominal pain domains (a total of 10 questions), which are each assessed on a scale of 1 (no discomfort at all) to 7 (very severe discomfort).

    The total CeD-GSRS score is calculated as the sum of the scores of all 10 questions, and ranges from 10 (no discomfort at all) to 70 (very severe discomfort in all celiac syndromes).

Sponsors and collaborators

Lead sponsor

Amgen

Industry

Registry information

Official study title

A Phase 2a, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of AMG 714 in Adult Patients With Celiac Disease

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Dec 22, 2015
Registry last updated
Dec 3, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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