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VTP-1000 in Adults With Celiac Disease

RecruitingEarly phase 1

A Phase 1, First in Human, Randomized, Placebo-controlled Trial With a Controlled Gluten Challenge to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of VTP-1000 in Adults With Celiac Disease

Who can join

Ages 18 to 70 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Diagnosis of celiac disease as confirmed by positive serology and intestinal histology
* Presence of Human Leukocyte Antigen (HLA)-DQ2.5 genotype
* Participants who are on a well controlled gluten restricted diet
* Anti-tissue transglutaminase (tTG) IgA antibodies less than 2 times the upper limit of normal and anti-deamidated gliadin peptide IgG (anti-DGP)-IgA/IgA antibodies less than 3 times the upper limit of normal
* Non-pregnant or breast feeding females
* No other clinical significant findings at screening

Exclusion Criteria:

* Refractory celiac disease
* Selective IgA deficiency
* Positive for HLA-DQ8
* Known wheat allergy or that is Type I hypersensitivity
* Active inflammatory bowel disease or other condition with symptoms that will be similar to celiac disease

About the study

GLU001 is a first-in-human clinical trial to assess the safety and tolerability of VTP-1000 for adults with celiac disease. This trial will assess VTP-1000 at various dose levels compared to placebo in a single ascending dose (SAD) and multiple ascending dose (MAD) format. Participants will be followed for a short period of time to assess the impact of VTP-1000 on their immune system (Adverse events, reactions in the blood, and physical exam differences). Participants enrolled in the MAD portion of the trial will undergo a gluten challenge to assess the impact exposure to gluten has on participants after administration of VTP-1000.

What is being tested

Sponsor: Barinthus Biotherapeutics · Participants: 45 · Started: Aug 1, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06310291

Locations in the U.S.

CaliforniaParexel EPCU LA, Los Angeles
ColoradoPeak Gastroenterology Associates, Colorado Springs
FloridaJacksonville Center for Clinical Research, Jacksonville
GCP Research, St. Petersburg
MarylandParexel EPCU Baltimore, Baltimore
MichiganClinical Research Institute of Michigan, Clinton Township
West Michigan Clinical Research Center, Wyoming
MinnesotaMayo Clinic, Rochester
New YorkNYU Langone - Gastroenterology Associates, New York
North CarolinaNorth Carolina Clinical Research, Raleigh
OhioCentricity Research, Columbus
TennesseeVanderbilt University Medical Center, Nashville
TexasPPD Research Unit, Austin
UtahVelocity Clinical Research, Salt Lake City, West Jordan
VirginiaClinical Research Partners, Richmond
WashingtonVelocity Clinical Research, Seattle, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.