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Completed Phase 2 Interventional Results available

PRV-015 in Gluten-free Diet Non-responsive Celiac Disease

ClinicalTrials.gov ID: NCT04424927

Public ClinicalTrials.gov record NCT04424927. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 4:28 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2b, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of PRV-015 in Adult Patients With Non-Responsive Celiac Disease as an Adjunct to a Gluten-free Diet

Study identification

NCT ID
NCT04424927
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Provention Bio, a Sanofi Company
Industry
Enrollment
388 participants

Conditions and interventions

Conditions

Interventions

  • PRV-015 Biological
  • Placebo Other

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 23, 2020
Primary completion
Jul 29, 2024
Completion
Jul 29, 2024
Last update posted
Oct 19, 2025

2020 – 2024

United States locations

U.S. sites
28
U.S. states
19
U.S. cities
28
Facility City State ZIP Site status
Clinical Site Los Angeles California 90036
Clinical Site Ventura California 93003
Clinical Site Denver Colorado 80209
Clinical Site Leesburg Florida 34748
Clinical Site Tampa Florida 33613
Clinical Site Winter Park Florida 32789
Clinical Site Chicago Illinois 60637
Clinical Trial Site Northbrook Illinois 60062
Clinical Trial Site Chevy Chase Maryland 20815
Clinical Site Boston Massachusetts 02111
Clinical Site Chesterfield Michigan 48047
Clinical Site Rochester Minnesota 55905
Clinical Site Morristown New Jersey 07960
Clinical Trial Site Brooklyn New York 11235
Clinical Site New Windsor New York 12553
Clinical Trial Site New York New York 10032
Clinical Site Raleigh North Carolina 27607
Clinical Trial Site Dublin Ohio 43016
Clinical Site Philadelphia Pennsylvania 19104
Clinical Site Uniontown Pennsylvania 14401
Clinical Site Warwick Rhode Island 02886
Clinical Trial Site North Charleston South Carolina 29405
Clinical Site Nashville Tennessee 37212
Clinical Trial Site Cedar Park Texas 78613
Clinical Site Garland Texas 75044
Clinical Site West Jordan Utah 84088
Clinical Site Bellevue Washington 98004
Clinical Site Tacoma Washington 98405

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04424927, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 19, 2025 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04424927 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →