A Randomized Double-blind Placebo-Controlled Parallel-Group Study to Evaluate the Efficacy and Safety of Intravenously Administered BMS-986168 in Participants with Progressive Supranuclear Palsy
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- STATUS
- Not Recruiting
Updated on 19 February 2024
Summary
The purpose of this study is to evaluate the efficacy and safety of intravenously administered BMS-986168 in participants with progressive supranuclear palsy (PSP).
Description
The purpose of this study is to evaluate the efficacy and safety of intravenously administered BMS-986168 in participants with progressive supranuclear palsy (PSP).
Details
| Condition | progressive supranuclear palsy |
|---|---|
| Age | 100years or below |
| Clinical Study Identifier | TX8011 |
| Last Modified on | 19 February 2024 |
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