RECRUITING

A Trial to Assess the Efficacy and Safety of TEV-53408 in Adults With Celiac Disease

Description

The primary efficacy objective of the trial is to assess the ability of TEV-53408 to attenuate gluten-induced enteropathy in adults with celiac disease. The primary safety objective of the trial is to assess the safety of TEV-53408 in adults with celiac disease. A secondary objective is to further assess the efficacy of TEV-53408 in adults with celiac disease. The expected trial duration per participant is approximately 86 weeks.

Conditions

Study Overview

Study Details

Study overview

The primary efficacy objective of the trial is to assess the ability of TEV-53408 to attenuate gluten-induced enteropathy in adults with celiac disease. The primary safety objective of the trial is to assess the safety of TEV-53408 in adults with celiac disease. A secondary objective is to further assess the efficacy of TEV-53408 in adults with celiac disease. The expected trial duration per participant is approximately 86 weeks.

A Multicenter, Randomized, Double-blind, Placebo-controlled, Phase 2a Trial to Characterize the Efficacy and Safety of TEV-53408 in Adults With Celiac Disease While Undergoing Oral Gluten Exposure

A Trial to Assess the Efficacy and Safety of TEV-53408 in Adults With Celiac Disease

Condition
Celiac Disease
Intervention / Treatment

-

Contacts and Locations

Colorado Springs

Teva Investigational Site 12131, Colorado Springs, Colorado, United States, 80907

Wyoming

Teva Investigational Site 12121, Wyoming, Michigan, United States, 49519

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Diagnosis of celiac disease at least 12 months prior to screening
  • * On a gluten-free diet for at least 12 months prior to screening
  • * Women must not be pregnant, lactating, breastfeeding, or planning pregnancy during the trial period
  • * Male participants (including vasectomized) with women of child-bearing potential partners (whether pregnant or not) must use condoms and also agree not to donate sperm for the designated period
  • * A diagnosis or suspicion of refractory celiac disease
  • * History of severe celiac-related symptoms following gluten exposure that require acute medical care or intervention of a health care professional
  • * Any other gastrointestinal disease or condition that may interfere with the assessment of celiac disease
  • * Current or history of malignancy or treatment of malignancy in the last 5 years, excluding treated basal cell carcinoma
  • * Pregnant or lactating woman, or plans to become pregnant during the trial; any man who is considering fathering a child or donating sperm during the trial
  • * A history of chronic alcohol or substance abuse disorder within the previous 2 years.
  • * An active infection(s) requiring treatment with intravenous (iv) anti-infectives (antibiotics, antivirals, antifungals) within 30 days prior to screening or oral anti-infectives (antibiotics, antivirals, antifungals) within 14 days prior to screening
  • * Received or intends to receive any live vaccine within 4 weeks or any non-live vaccine 2 weeks prior to investigational medicinal product administration.

Ages Eligible for Study

18 Years to 64 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Teva Branded Pharmaceutical Products R&D, Inc.,

Teva Medical Expert, MD, STUDY_DIRECTOR, Teva Branded Pharmaceutical Products R&D, Inc.

Study Record Dates

2027-09-14