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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 Oct 18, 2026, 12:34 PM 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the safety and efficacy of tulisokibart (MK-7240) in participants with moderately to severely active Crohn's Disease. After the completion of the 12-week Induction Period, eligible participants have the option to enter an Open-label Extension (OLE) Period for up to 170 weeks.

Study identification

NCT ID
NCT05013905
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
55 participants

Conditions and interventions

Conditions

Interventions

Biological · Diagnostic Test

Eligibility (public fields only)

Age range
18 Years and older
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
Jul 28, 2021 (Actual)
Primary completion
Sep 23, 2022 (Actual)
Completion
May 27, 2025 (Actual)
Last update posted
Jul 22, 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 Jul 22, 2026 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05013905 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →