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Clinical Trials in the EU / 2025-520721-21-00
Terminated Phase II

A Phase 2, Multicenter, Platform Study of Targeted Therapies for the Treatment of Adult Subjects with Moderately to Severely Active Rheumatoid Arthritis.

2025-520721-21-00 · tracked via the Priya Life Science EU tracker
Sponsor
AbbVie Deutschland GmbH & Co. KG
Sponsor type
Pharmaceutical company
Therapeutic area
Immune System Diseases
Decision date
12/09/2025
Enrollment target
108
Sites
Germany, Czechia, Hungary, Spain, Poland, Slovakia

Condition studied

Rheumatoid Arthritis

Investigational medicinal product(s)

LutikizumabUSP/Ph. Eur.ABBV-323Universal Placebo (LutikizumabRavagalimab)

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Percentage of Participants With an American College of Rheumatology 50% (ACR50) Response at Week 12

Endpoint detail

Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 12, Percentage of Participants With an American College of Rheumatology 70% (ACR70) Response at Week 12, Percentage Of Participants Achieving Low Disease Activity (LDA) per Disease Activity Score-28 With C-Reactive Protein (DAS28-CRP) at Week 12, Percentage Of Participants Achieving Clinical Remission (CR) per DAS28 (CRP) at Week 12, Change from Baseline in DAS28 (CRP) at Week 12, Percentage Of Participants Achieving LDA per Clinical Disease Activity Index (CDAI) at Week 12, Percentage Of Participants Achieving CR per CDAI at Week 12

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-520721-21-00 on CTIS ↗ ← All trials in the EU