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A Study to Investigate Canvuparatide Compared With Placebo in Adult Patients With Hypoparathyroidism
Sponsor: MBX Biosciences
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
Conditions
Interventions
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.
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