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Latiglutenase Protects the Mucosa and Attenuates Symptom Severity in Patients With Celiac Disease Exposed to a Gluten Challenge.
Murray, Joseph A; Syage, Jack A; Wu, Tsung-Teh; Dickason, Matthew A; Ramos, Ana G; Van Dyke, Carol; Horwath, Irina; Lavin, Philip T; Mäki, Markku; Hujoel, Isabel; Papadakis, Konstantinos A; Bledsoe, Adam C; Khosla, Chaitan; Sealey-Voyksner, Jennifer A.
Afiliación
  • Murray JA; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota. Electronic address: murray.joseph@mayo.edu.
  • Syage JA; ImmunogenX, Inc, Newport Beach, California.
  • Wu TT; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
  • Dickason MA; ImmunogenX, Inc, Newport Beach, California.
  • Ramos AG; ImmunogenX, Inc, Newport Beach, California.
  • Van Dyke C; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
  • Horwath I; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
  • Lavin PT; Boston Biostatistics Research Foundation, Framingham, Massachusetts.
  • Mäki M; Faculty of Medicine and Health Technology, Tampere University and Tampere University Hospital, Tampere, Finland.
  • Hujoel I; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
  • Papadakis KA; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
  • Bledsoe AC; Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
  • Khosla C; Stanford University, Stanford, California.
  • Sealey-Voyksner JA; ImmunogenX, Inc, Newport Beach, California.
Gastroenterology ; 163(6): 1510-1521.e6, 2022 12.
Article en En | MEDLINE | ID: mdl-35931103
ABSTRACT
BACKGROUND &

AIMS:

Gluten ingestion in patients with celiac disease can lead to gastrointestinal symptoms and small intestinal mucosal injury.

METHODS:

This gluten challenge phase 2 trial was double blind and placebo controlled, and it assessed the efficacy and safety of a 1200-mg dose of IMGX003 in patients with celiac disease exposed to 2 g of gluten per day for 6 weeks. The change in the ratio of villus height to crypt depth was the primary endpoint. Secondary endpoints included density of intraepithelial lymphocytes and symptom severity. These endpoints were evaluated by analysis of covariance. Additional endpoints included serology and gluten-immunogenic peptides in urine.

RESULTS:

Fifty patients were randomized, and 43 patients completed the study (IMGX003, n = 21; placebo, n = 22). The mean change in the ratio of villus height to crypt depth (primary endpoint) for IMGX003 vs placebo was -0.04 vs -0.35 (P = .057). The mean change in the density of intraepithelial lymphocytes (secondary endpoint) for IMGX003 vs placebo was 9.8 vs 24.8 cells/mm epithelium (P = .018). The mean change (worsening) in symptom severity in relative units (secondary endpoint) for IMGX003 vs placebo was 0.22 vs 1.63 (abdominal pain, P = .231), 0.96 vs 3.29 (bloating, P = .204), and 0.02 vs 3.20 (tiredness, P = .113). The 3 × 2-week trend line significance values for these symptoms, respectively, were P = .014, .030, and .002.

CONCLUSIONS:

IMGX003 reduced gluten-induced intestinal mucosal damage and symptom severity. (ClinicalTrials.gov, Number NCT03585478).
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad Celíaca / Glútenes Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Humans Idioma: En Revista: Gastroenterology Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad Celíaca / Glútenes Tipo de estudio: Clinical_trials / Diagnostic_studies Límite: Humans Idioma: En Revista: Gastroenterology Año: 2022 Tipo del documento: Article