A Phase 2 Safety and Efficacy Study of Tulisokibart (MK-7240/PRA023) in Subjects With Moderately to Severely Active Ulcerative Colitis (MK-7240-005)

Last updated:
2026-07-11
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View trial details

Overview

Official protocol title:

A PHASE 2, MULTI-CENTER, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE SAFETY, EFFICACY, AND PHARMACOKINETICS OF INDUCTION THERAPY WITH PRA023 IN SUBJECTS WITH MODERATELY TO SEVERELY ACTIVE ULCERATIVE COLITIS

Intervention/treatment:
PRA023
Medical condition:
ULCERATIVE COLITIS
Protocol code:
PR200-102
Control number:
252496
Status:
Closed
Approved:
June 04, 2021
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT04996797
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: ALL
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Senior Vice President, Global Clinical Development
Organization
Merck Sharp and Dohme LLC
Phone:
1-800-672-6372
Sponsor
PROMETHEUS BIOSCIENCES, INC.

Locations

Alberta

Prometheus Biosciences Selected Site
Calgary, Alberta, T2N 4Z6

British Columbia

Prometheus Biosciences Selected Site
Vancouver, British Columbia, V6Z2K5

Nova Scotia

Prometheus Biosciences Selected Site
Halifax, Nova Scotia, B3H 1V7

Ontario

Prometheus Biosciences Selected Site
North York, Ontario, M6A 3B4

Results

See the results from the trial NCT04996797. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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