drugset / Trial / NCT06036784

Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Study of MBX 1416 in Healthy Subjects

NCT06036784

Phase 1 Completed 69 enrolled MBX Biosciences ProSciento, Inc. · collab
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

EvaluationDrugModalityDoseRoute
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