Active, not recruitingPhase 2NCT05270668

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)

Studying Diffuse cutaneous systemic sclerosis

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Prometheus Biosciences, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
Principal Investigator
Prometheus Biosciences
Clinical Trials Call Center
Intervention
Tulisokibart(drug)
Enrollment
154 enrolled
Eligibility
18 years · All sexes
Timeline
20222029

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05270668 on ClinicalTrials.gov

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