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Completed Phase 2 Interventional Results available

A Phase 2a Safety and Efficacy Open-Label Study of Tulisokibart (MK-7240/PRA023) in Participants With Moderately to Severely Active Crohn's Disease (MK-7240-006)

ClinicalTrials.gov ID: NCT05013905

Public ClinicalTrials.gov record NCT05013905. 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 Apr 22, 2026, 8:34 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 2a, Multi-Center, Open-Label Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of PRA023 in Subjects With Moderately to Severely Active Crohn's Disease

Study identification

NCT ID
NCT05013905
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Prometheus Biosciences, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
Industry
Enrollment
55 participants

Conditions and interventions

Conditions

Interventions

  • Companion Diagnostic (CDx) Diagnostic Test
  • Tulisokibart Biological

Diagnostic Test · Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Not listed

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

Study timeline

Start date
Jul 27, 2021
Primary completion
Sep 22, 2022
Completion
May 26, 2025
Last update posted
Apr 20, 2026

2021 – 2025

United States locations

U.S. sites
16
U.S. states
8
U.S. cities
14
Facility City State ZIP Site status
Prometheus Biosciences Selected Site Los Angeles California 90045
Prometheus Biosciences Selected Site Los Angeles California 90048
Prometheus Biosciences Selected Site Liberty Kansas 64098
Prometheus Biosciences Selected Site Chesterfield Michigan 48047
Prometheus Biosciences Selected Site Ypsilanti Michigan 48197
Prometheus Biosciences Selected Site St Louis Missouri 63141
Prometheus Biosciences Selected Site Lebanon New Hampshire 03756
Prometheus Biosciences Selected Site New York New York 10065
Prometheus Biosciences Selected Site Garland Texas 75044
Prometheus Biosciences Selected Site Lubbock Texas 79410
Prometheus Biosciences Selected Site Lubbock Texas 79424
Prometheus Biosciences Selected Site San Antonio Texas 78229
Prometheus Biosciences Selected Site Southlake Texas 78229
Prometheus Biosciences Selected Site Tyler Texas 75702
Prometheus Biosciences Selected Site Bellevue Washington 98004
Prometheus Biosciences Selected 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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05013905, 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 Apr 20, 2026 · Synced Apr 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05013905 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →