This study is investigating the safety and efficacy of eneboparatide (AZP-3601) in patients with chronic hypoparathyroidism (cHP). During the first 24 weeks of the trial, participants will be randomized to receive eneboparatide or placebo. Study treatment is blinded: patients and doctors will not know which group each patient has been randomized to. All patients will start with a fixed dose of study treatment (eneboparatide or placebo), administered subcutaneously with a pre-filled pen. Study treatment will be individually titrated. After completion of the first 24 weeks, patients will be treated in the open label extension part of the study for 132 weeks. During this phase, all patients (including patients that were in the placebo group) will receive eneboparatide.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
165
Supplied as a solution (concentration of 250 mcg/mL or 500 mcg/mL) in single-patient-use prefilled pens
Placebo is supplied as a solution (containing the excipient solution for eneboparatide) in single-patient-use prefilled pens
Harbor UCLA Medical Center Endocrinology
Torrance, California, United States
Denver Endocrinology Diabetes and Thyroid Center
Denver, Colorado, United States
University of Chicago - Medical Center
Chicago, Illinois, United States
North Shore University Health System
Evanston, Illinois, United States
Indiana University (IU) Health University Hospital
Indianapolis, Indiana, United States
Efficacy - Primary Endpoint
After 24 weeks of treatment, the proportion of patients in the eneboparatide treatment group vs. placebo: * Achieving complete independence from active vitamin D; * Achieving independence from therapeutic doses of oral calcium (i.e. taking oral elemental calcium supplements ≤600 mg/day); and * With albumin-adjusted serum calcium within the normal range (8.3 to 10.6 mg/dL).
Time frame: 24 weeks
Hypercalciuria
Proportion of patients who had hypercalciuria at baseline and normalize 24-hour urinary calcium excretion level (i.e., achieve \<250 mg/24 hours for females or \<300 mg/24 hours for males)
Time frame: 24 weeks
Change from baseline in the HPT-DD-SE - Physical Domain score
Change from baseline in patient's symptoms, as assessed by the average weekly HPT-DD-SE physical domain score in the eneboparatide treatment group vs. placebo
Time frame: 24 weeks
Change from baseline in the HPT-DD-SE - Cognitive Domain score
Change from baseline in patient's symptoms, as assessed by the average weekly HPT-DD-SE cognitive domain score in the eneboparatide treatment group vs. placebo
Time frame: 24 weeks
Change from baseline in the HPT-LIQ - Physical Functioning Domain score
Change from baseline in the HPT-LIQ Physical Functioning domain score, in the eneboparatide treatment group vs. placebo
Time frame: 24 weeks
Change from baseline in the SF-36 Physical Functioning subscore
Change from baseline in the SF-36 Physical Functioning subscore in the eneboparatide treatment group vs. placebo
Time frame: 24 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Massachusetts General Hospital
Boston, Massachusetts, United States
Mayo Clinic
Rochester, Minnesota, United States
Northern Nevada Endocrinology
Reno, Nevada, United States
Colombia University Irving Medical Center
New York, New York, United States
Physician's East Endocrinology
Greenville, North Carolina, United States
...and 44 more locations