This study will investigate how LY2127399 works in participants with rheumatoid arthritis (RA) who are not adequately responding to methotrexate. Participants will receive LY2127399 via an injection(s) under the skin at 4 week intervals for up to 52 weeks. Key study procedures include biopsies of the lining of an inflamed joint and blood tests to measure RA activity.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
2
Administered subcutaneously
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Frederick, Maryland, United States
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Battle Creek, Michigan, United States
Percent Change in Synovitis Scores From Baseline up to Week 16
Primary and secondary analyses were not conducted given insufficient data due to termination of the trial.
Time frame: Baseline up to Week 16
Percent Change in Synovial B Cell Mass From Baseline up to Week 16
Primary and secondary analyses were not conducted given insufficient data due to termination of the trial.
Time frame: Baseline up to Week 16
Percent Change in Synovial Immunoglobulin (Ig) Synthesis From Baseline up to Week 16
Primary and secondary analyses were not conducted given insufficient data due to termination of the trial.
Time frame: Baseline up to Week 16
Percent Change in Various Cell Types in the Blood From Baseline up to Week 24
Primary and secondary analyses were not conducted given insufficient data due to termination of the trial.
Time frame: Baseline up to Week 24
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Mayfield, Ohio, United States
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
Mesquite, Texas, United States