drugset / Trial / NCT06036784
Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of MBX 1416 in Healthy Subjects
RandomizedSequentialDouble-blindBasic science
Summary
The purpose of this trial is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of single and multiple doses and Drug Drug Interaction of MBX 1416 in healthy volunteers This study includes 3 parts. Part A involves a single dose of MBX 1416 or placebo taken as a subcutaneous injection (SC). Part B involves repeat doses of MBX 1416 or placebo taken as a subcutaneous injection (SC). Part C involves the evaluation of rosuvastatin and acetaminophen pharmacokinetics in the presence and absence of MBX 1416.
Timeline
- Start
- 2023-09-18
- Primary completion
- 2024-11-14
- Completion
- 2024-12-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Acetaminophen | Small molecule | — | — |
| Subject | MBX 1416 | Unknown | 10 mg | Subcutaneous |
| Subject | MBX 1416 | Unknown | 30 mg | Subcutaneous |
| Subject | MBX 1416 | Unknown | 100 mg | Subcutaneous |
| Subject | MBX 1416 | Unknown | 200 mg | Subcutaneous |
| Subject | Rosuvastatin | Small molecule | — | — |