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A Phase 2b, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Tulisokibart in Participants With Rheumatoid Arthritis

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-521745-25-00
Acronym
MK-7240-014
Enrollment
58
Registered
2025-10-27
Start date
2025-11-06
Completion date
Unknown
Last updated
2025-10-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rheumatoid Arthritis

Brief summary

Proportion of Participants Achieving American College of Rheumatology 20% Response Criteria (ACR20) at Week 12

Detailed description

Proportion of Participants Achieving American College of Rheumatology 50% Response Criteria (ACR50) at Week 12, Proportion of Participants Achieving American College of Rheumatology 70% Response Criteria (ACR70) at Week 12, Proportion of Participants Achieving Low Disease Activity (LDA) based on Disease Activity Score 28 Using C-Reactive Protein (DAS28-CRP), Change From Baseline in the Health Assessment Questionnaire Disability Index (HAQ-DI) Score at Week 12, Number of Participants Who Experience One or More Adverse Events (AEs), Number of Participants Who Discontinue Study Intervention Due to an AE

Interventions

Sponsors

Merck Sharp & Dohme LLC
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Proportion of Participants Achieving American College of Rheumatology 20% Response Criteria (ACR20) at Week 12

Secondary

MeasureTime frame
Proportion of Participants Achieving American College of Rheumatology 50% Response Criteria (ACR50) at Week 12, Proportion of Participants Achieving American College of Rheumatology 70% Response Criteria (ACR70) at Week 12, Proportion of Participants Achieving Low Disease Activity (LDA) based on Disease Activity Score 28 Using C-Reactive Protein (DAS28-CRP), Change From Baseline in the Health Assessment Questionnaire Disability Index (HAQ-DI) Score at Week 12, Number of Participants Who Experience One or More Adverse Events (AEs), Number of Participants Who Discontinue Study Intervention Due to an AE

Countries

Germany, Poland, Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026