Hypoparathyroidism
Conditions
Keywords
Hypoparathyroidism, Hypopara, HPTH, Hypocalcemia, Hypercalciuria, PTH, PTH(1-84)
Brief summary
This is an open-label study of PTH(1-84) treatment that seeks: 1. To determine the actions of PTH(1-84) to provide long term control of serum calcium and urinary calcium excretion with use of standard amounts of calcium and vitamin D supplementation. 2. To determine the extent to which PTH(1-84) improves quality-of-life on long-term basis. 3. To establish the safety of PTH(1-84) when administered for up to 12 years. 4. To attempt to quantify improvements in the typical signs/symptoms of hypoparathyroidism post PTH administration. There will be one visit conducted every six months in the study offices of the principal investigator, Dr. John Bilezikian. In addition to these visits, there will be, for new patients who have not used PTH (1-84) before, a Screening Visit four weeks prior to the baseline visit for the purpose of performing screening labs as well as a Pre-Baseline Local Quest Lab performed to ensure stability prior to Baseline.
Detailed description
Hypoparathyroidism is a rare disorder in which parathyroid hormone (PTH) is markedly decreased or absent from the circulation. It is the only remaining hormone deficiency state for which replacement with the missing hormone has been heretofore unavailable. The hypoparathyroid state is due either to autoimmune destruction of the parathyroid glands or to loss of parathyroid function after neck surgery. Without PTH, calcium homeostasis is markedly abnormal, the most salient clinical feature of which is a reduced serum calcium concentration. The hypocalcemia is associated with other important abnormalities such as markedly reduced parameters of bone turnover. PTH(1-84) is the ideal therapeutic approach to hypoparathyroidism. The current mainstay of therapy, calcium and vitamin D, has important clinical limitations. Large doses of calcium and vitamin D are required and often associated with hypercalciuria and vitamin D toxicity. Moreover, this approach does not correct the skeletal deficiencies resident in the bones themselves due to lack of PTH. In contrast, PTH(1-84) replaces precisely what is missing in this disorder. The research question is: What are the long-term safety and efficacy parameters of PTH(1-84) therapy in hypoparathyroidism? Preliminary data suggest that treatment with PTH(1-84) for up to 4 years improves control of the serum and urine calcium concentration safely. Since hypoparathyroidism is a chronic disorder, it is important to know whether these salutary effects continue to be seen beyond 4 years. There is a need to determine the safety and efficacy treatment of PTH(1-84) in hypoparathyroidism beyond 4 years.
Interventions
open label PTH(1-84) at either 25mcg every other day, 25mcg every day, 50mcg daily, 75mcg daily, or 100mcg daily
Sponsors
Study design
Eligibility
Inclusion criteria
For Returning Participants or participants graduating from one of the parent studies: Inclusion Criteria: * Must have participated in and concluded the CL1-11-040, PAR-C10-007 or PAR-C10-008 Study at any site in the continental United States * Must have participated in and concluded the Hypopara Study at Columbia University
Exclusion criteria
* failure to have completed either of the inclusionary studies For New Participants (20 anticipated): INCLUSION CRITERIA: 1. Signed and dated informed consent form (ICF) before any study-related procedures are performed. 2. Adult males or females 18 to 85 years of age. 3. History of hypoparathyroidism for ≥ 18 months, including evidence of hypocalcemia and concomitant serum intact PTH concentrations below the lower limit of normal within 12 months prior to Baseline. 4. Requirement for calcitriol ≥0.25 mcg per day per day prior to Baseline. 5. Requirement for supplemental oral calcium ≥ 1500 mg per day between supplemental and dietary sources. 6. Serum thyroid function tests within normal laboratory limits at screening for all subjects not receiving thyroid hormone replacement therapy. For patients on thyroid hormone replacement therapy, the dose must have been stable for at least 3 months prior to screening 7. serum creatinine \< 1.5 mg/dL on a single measurement prior to use of study drug 8. Physically capable of performing daily subcutaneous (SQ) self-injections, in the thigh, of study medication (or have designee perform injection). 9. Willingness and ability to comply with the protocol (prior to screening). 10. With regard to female patients: Women of childbearing potential must have a negative pregnancy test at Screening and agree to use two medically acceptable methods of contraception for the duration of the study with pregnancy testing at every scheduled visit.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in Dose of Calcium Supplementation | Baseline, up to 4 years | Serum and urinary calcium levels maintained by change in requirements for calcium supplementation. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Percent Change in BMD by DXA | Baseline, up to 4 years | Bone Mineral Density (BMD) as measured by Dual Energy X-Ray Absorptiometry (DXA) |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Open-label PTH(1-84) open-label PTH(1-84) / variable dosing: 25mcg every other day, 25mcg every day, 50mcg every day, 75mcg every day, 100mcg every day | 62 |
| Total | 62 |
Baseline characteristics
| Characteristic | Open-label PTH(1-84) |
|---|---|
| Age, Customized 18-21 years | 0 Participants |
| Age, Customized 22-29 years | 5 Participants |
| Age, Customized 30-39 years | 7 Participants |
| Age, Customized 40-49 years | 22 Participants |
| Age, Customized 50-59 years | 13 Participants |
| Age, Customized 60-69 years | 13 Participants |
| Age, Customized 70-79 years | 2 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants |
| Race (NIH/OMB) Asian | 2 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) White | 60 Participants |
| Region of Enrollment United States | 62 participants |
| Sex: Female, Male Female | 50 Participants |
| Sex: Female, Male Male | 12 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 0 / 62 |
| other Total, other adverse events | 27 / 62 |
| serious Total, serious adverse events | 25 / 62 |
Outcome results
Change in Dose of Calcium Supplementation
Serum and urinary calcium levels maintained by change in requirements for calcium supplementation.
Time frame: Baseline, up to 4 years
Population: Analyzed data from this cohort included 27 evaluable subjects treated with open-label PTH(1-84) for 4 years.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Open-label PTH(1-84) | Change in Dose of Calcium Supplementation | 37 percent change in dose | Standard Deviation 43 |
Percent Change in BMD by DXA
Bone Mineral Density (BMD) as measured by Dual Energy X-Ray Absorptiometry (DXA)
Time frame: Baseline, up to 4 years
Population: Analyzed data from this cohort included 27 evaluable subjects treated with open-label PTH(1-84) for 4 years.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Open-label PTH(1-84) | Percent Change in BMD by DXA | 5.5 percent change in BMD | Standard Deviation 9 |