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Safety, Pharmacokinetics and Efficacy of MBX 2109 in Patients With Hypoparathyroidism

Hypoparathyroidism Clinical Trial

Official title:
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase 2 Trial to Evaluate the Safety, Pharmacokinetics, and Efficacy of MBX 2109 in Patients With Hypoparathyroidism (Avail Study)

Clinical Trial Summary

The purpose of this study is to investigate the safety and tolerability of MBX 2109 administered once weekly to patients with hypoparathyroidism.

Clinical Trial Description

This study is to investigate the safety, pharmacokinetics, and efficacy of MBX 2109 administered once weekly to patients with hypoparathyroidism. Given MBX 2109 is intended as a PTH replacement hormone to demonstrate that MBX 2109 can maintain serum calcium within a normal range without the need for active vitamin D and therapeutic calcium supplements. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06465108
Study type Interventional
Source MBX Biosciences
Contact Kirk Ways, MD, PhD
Phone 844-877-4473
Email kways@mbxbio.com
Status Recruiting
Phase Phase 2
Start date June 7, 2024
Completion date June 2025
View Details
See also
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