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Study identifier: NCT05270668 Synced from ClinicalTrials.gov · August 05, 2026
● Active Not Recruiting

Phase 2 Safety and Efficacy Study of Tulisokibart (MK-7240/PRA023) in Subjects With Systemic Sclerosis Associated With Interstitial Lung Disease (SSc-ILD) (MK-7240-007)

Condition: Diffuse Cutaneous Systemic Sclerosis · Interstitial Lung Disease  ·  Sponsor: Prometheus Biosciences, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)

PhasePhase 2
Planned participants154
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to assess the safety and efficacy of tulisokibart in participants with SSc-ILD.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (95)

Mayo Clinic - Scottsdale ( Site 4014)Phoenix, Arizona, United States
Pacific Arthritis Care Center ( Site 4008)Los Angeles, California, United States
Cedars Sinai Medical Center ( Site 4010)Los Angeles, California, United States
UCLA School of Medicine ( Site 4006)Los Angeles, California, United States
Stanford Health Care ( Site 4009)Palo Alto, California, United States
National Jewish Health Medical Center ( Site 4015)Denver, Colorado, United States
Yale University ( Site 4017)New Haven, Connecticut, United States
MedStar Georgetown University Hospital ( Site 4005)Washington D.C., District of Columbia, United States
Johns Hopkins Asthma and Allergy Center [Baltimore, MD] ( Site 4018)Baltimore, Maryland, United States
Massachusetts General Hospital ( Site 4003)Boston, Massachusetts, United States
Boston University School of Medicine ( Site 4021)Boston, Massachusetts, United States
University of Michigan Hospital ( Site 4001)Ann Arbor, Michigan, United States

+ 83 more locations — full list on the registry record.

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