WHO ICTRP trial

A Phase II Study of Abatacept Versus Placebo to Assess the Prevention of…

ACTRN12605000785606 · Australian New Zealand Clinical Trials Registry (ANZCTR) · Not Recruiting

Key facts

Trial ID ACTRN12605000785606
Public title A Phase II Study of Abatacept Versus Placebo to Assess the Prevention of Rheumatoid Arthritis (RA) in Adult Patients With Undifferentiated Arthritis Who Are at High Risk for the Development of RA
Scientific title A Phase II Study of Abatacept Versus Placebo to Assess the Prevention of Rheumatoid Arthritis (RA) in Adult Patients With Undifferentiated Arthritis Who Are at High Risk for the Development of RA
Primary sponsor Bristol-Myers Squibb Australia
Registry Australian New Zealand Clinical Trials Registry (ANZCTR)
Recruitment status Not Recruiting
Study type Interventional
Phase Phase 2
Countries Australia
Conditions Undifferentiated Arthritis (UA); Undifferentiated Arthritis (UA);Inflammatory and Immune System - Rheumatoid arthritis
Interventions Drug: Abatacept for the first 6 months, then 18 months oberservation. Study Design: Educational/Counseling/Training, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study
Registration date Sep 12, 2005
Target size 50
Secondary IDs Bristol Myers Squibb: IM101-046
Registry page anzctr.org.au

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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