drugset / Trial / NCT04855201
A Study to Evaluate ASP0367 in Participants With Reduced Maximum Oxygen Uptake Due to Poor Systemic Oxygen Extraction
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The purpose of this study is to to evaluate the effect of ASP0367 on improvement of aerobic capacity relative to placebo, as well as evaluate the safety and tolerability of ASP0367 relative to placebo. This study will also evaluate the effect of ASP0367 on improvement of other aerobic capacity parameters relative to placebo, as well as evaluate the effect of ASP0367 on improvement of functional capacity relative to placebo.
Timeline
- Start
- 2021-06-14
- Primary completion
- 2022-12-16
- Completion
- 2022-12-16
Outcome
Outcome not reported
Stopped: “Lack of Pharmacological effect”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bocidelpar | Small molecule | — | Oral |
Indications
No indication recorded.