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RECRUITING
NCT07699471
PHASE3

A Study to Investigate Canvuparatide Compared With Placebo in Adult Patients With Hypoparathyroidism

Sponsor: MBX Biosciences

View on ClinicalTrials.gov

Summary

The purpose of this study is to investigate the efficacy and safety of canvuparatide administered as a once-weekly (QW) treatment to adult study participants with hypoparathyroidism (HypoPT).

Official title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Followed by an Open-Label Extension to Evaluate the Safety and Efficacy of Canvuparatide (MBX 2109) in Adult Patients With Hypoparathyroidism

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2026-08

Completion Date

2029-08

Last Updated

2026-08-27

Healthy Volunteers

No

Interventions

DRUG

Canvuparatide

• Drug per vial: Each DDC contains 1 vial of lyophilized drug product. The reconstituted strengths are 400 μg/mL, 600 μg/mL, 800 μg/mL, 1000 μg/mL, 1200 μg/mL, 1400 μg/mL, and 1600 μg/mL.

OTHER

Placebo

• Drug per vial: Each DDC contains 1 vial of lyophilized drug product. The reconstituted strengths are 400 μg/mL, 600 μg/mL, 800 μg/mL, 1000 μg/mL, 1200 μg/mL, 1400 μg/mL, and 1600 μg/mL.

Locations (10)

MBX Biosciences Investigational Site

Los Angeles, California, United States

MBX Biosciences Investigational Site

Homestead, Florida, United States

MBX Biosciences Investigational Site

Las Vegas, Nevada, United States

MBX Biosciences Investigational Site

Reno, Nevada, United States

MBX Biosciences Investigational Site

Greenville, North Carolina, United States

MBX Biosciences Investigational Site

Dallas, Texas, United States

MBX Biosciences Investigational Site

Round Rock, Texas, United States

MBX Biosciences Investigational Site

Shavano Park, Texas, United States

MBX Biosciences Investigational Site

Weslaco, Texas, United States

MBX Biosciences Investigational Site

Spokane, Washington, United States