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HEXT (Hypo EXTended): Effect of PTH on Skeleton in Hypoparathyroidism

HEXT: The Hypoparathyroidism Studies, EXTended: The Effect of PTH on the Skeleton in Hypoparathyroidism

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01199614
Enrollment
62
Registered
2010-09-13
Start date
2009-12-31
Completion date
2017-06-26
Last updated
2024-07-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypoparathyroidism

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

DRUGopen-label PTH(1-84)

open label PTH(1-84) at either 25mcg every other day, 25mcg every day, 50mcg daily, 75mcg daily, or 100mcg daily

Sponsors

NPS Pharma
CollaboratorINDUSTRY
Shire
CollaboratorINDUSTRY
Columbia University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

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

MeasureTime frameDescription
Change in Dose of Calcium SupplementationBaseline, up to 4 yearsSerum and urinary calcium levels maintained by change in requirements for calcium supplementation.

Secondary

MeasureTime frameDescription
Percent Change in BMD by DXABaseline, up to 4 yearsBone Mineral Density (BMD) as measured by Dual Energy X-Ray Absorptiometry (DXA)

Countries

United States

Participant flow

Participants by arm

ArmCount
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
Total62

Baseline characteristics

CharacteristicOpen-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 typeEG000
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

Primary

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.

ArmMeasureValue (MEAN)Dispersion
Open-label PTH(1-84)Change in Dose of Calcium Supplementation37 percent change in doseStandard Deviation 43
Secondary

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.

ArmMeasureValue (MEAN)Dispersion
Open-label PTH(1-84)Percent Change in BMD by DXA5.5 percent change in BMDStandard Deviation 9

Source: ClinicalTrials.gov · Data processed: Feb 15, 2026