Condition: Systemic Lupus Erythematosus · Sponsor: Bristol-Myers Squibb
The purpose of this study is to evaluate the effectiveness, safety and tolerability of Afimetoran in participants with active Systemic Lupus Erythematosus (SLE). The extension period will provide additional long-term safety and efficacy data and enable those participants initially randomized to placebo to receive treatment with Afimetoran.
This description comes directly from the study's public registry record.
No contact information is available for this study as per the public registry record.
Always discuss trial participation with your own doctor first.
| Local Institution - 0100 | Birmingham, Alabama, United States | — |
| Local Institution - 0123 | Huntington Beach, California, United States | — |
| Local Institution - 0170 | La Jolla, California, United States | — |
| Local Institution - 0159 | La Palma, California, United States | — |
| Local Institution - 0172 | San Diego, California, United States | — |
| Local Institution - 0164 | Woodland Hills, California, United States | — |
| Local Institution - 0121 | Clearwater, Florida, United States | — |
| Local Institution - 0167 | Kissimmee, Florida, United States | — |
| Local Institution - 0122 | Orlando, Florida, United States | — |
| Local Institution - 0173 | Ormond Beach, Florida, United States | — |
| Local Institution - 0154 | Plantation, Florida, United States | — |
| Local Institution - 0137 | South Miami, Florida, United States | — |
+ 135 more locations — full list on the registry record.
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