drugset / Trial / NCT07029412

Study to Evaluate Efficacy and Dose Response of Imapextide (STEADI)

NCT07029412

Phase 2 Completed 20 enrolled MBX Biosciences
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the preliminary efficacy of single SC administration of MBX 1416 at different dose levels in patients with PBH

Timeline

Start
2025-08-26
Primary completion
2026-04-18
Completion
2026-05-01

Drugs

EvaluationDrugModalityDoseRoute
Subject MBX 1416 Unknown Subcutaneous