A Study to Investigate Canvuparatide Compared With Placebo in Adult Patients With Hypoparathyroidism
Start Date
8/26/2026
Completion Date
8/1/2029
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).
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
Canvuparatide
Placebo
Conditions
Locations
MBX Biosciences Investigational Site
Englewood, Colorado 80113
United States
MBX Biosciences Investigational Site
Homestead, Florida 33030
United States
MBX Biosciences Investigational Site
Lawrenceville, Georgia 30046
United States
MBX Biosciences Investigational Site
Metairie, Louisiana 70002
United States
MBX Biosciences Investigational Site
Jackson, Mississippi 39202
United States
MBX Biosciences Investigational Site
Las Vegas, Nevada 89148
United States
MBX Biosciences Investigational Site
Reno, Nevada 89511
United States
MBX Biosciences Investigational Site
Albany, New York 12208
United States
MBX Biosciences Investigational Site
Syracuse, New York 13210
United States
MBX Biosciences Investigational Site
The Bronx, New York 10467
United States
MBX Biosciences Investigational Site
Greenville, North Carolina 27834
United States
MBX Biosciences Investigational Site
Columbus, Ohio 43210
United States
MBX Biosciences Investigational Site
Summerville, South Carolina 29485
United States
MBX Biosciences Investigational Site
Dallas, Texas 75208
United States
MBX Biosciences Investigational Site
Edinburg, Texas 78539
United States
MBX Biosciences Investigational Site
Round Rock, Texas 78681
United States
MBX Biosciences Investigational Site
Shavano Park, Texas 78231
United States
MBX Biosciences Investigational Site
Weslaco, Texas 78596
United States
MBX Biosciences Investigational Site
Spokane, Washington 99216
United States