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A Registry for Participants With Chronic Hypoparathyroidism

Completed · NCT01922440

Conditions: Hypoparathyroidism

At a glance

Research payments reported, 2025
$143,851
U.S. investigators named
28
Sites paid
27
Planned or actual enrollment
1,339

About the trial

Sponsor
Takeda (with Takeda Development Center Americas, Inc.)
Tested
No intervention (other)
Dates
Started 2013-07-30; completion 2026-06-30
Results posted
Not yet

The main aim of this study is to find out the long-term safety and effectiveness profile of recombinant human parathyroid hormone (1-84) (rhPTH\[1-84\]) treatment in participants with chronic hypoparathyroidism under conditions of routine clinical practice. Participants will be treated according to their clinic's standard practice determined by the treating doctors. Each participant will fill out a study questionnaire during a routine doctor visit.

From ClinicalTrials.gov, last updated 2026-07-14. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Takeda Pharmaceuticals U.S.A., Inc. reported $143,851 in research payments for this study in 2025 (169 payments).

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.