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A Study to Evaluate Safety, Efficacy and Pharmacokinetics of Paricalcitol For Treatment of Secondary Hyperparathyroidism (SHPT) in Pediatric Participants With Stage 5 Chronic Kidney Disease (CKD)

Terminated · Phase 3 · NCT04064827

Conditions: Chronic Kidney Disease (CKD), Secondary Hyperparathyroidism (SHPT)

At a glance

Research payments reported, 2025
$107,810
U.S. investigators named
7
Sites paid
7
Planned or actual enrollment
2

About the trial

Sponsor
AbbVie
Tested
Paricalcitol (drug)
Dates
Started 2020-09-16; completion 2025-06-09
Results posted
Yes

The main objective of this study is to evaluate the safety, efficacy and pharmacokinetics of paricalcitol oral solution in pediatric participants of ages 0 to 9 years with SHPT associated with stage 5 CKD receiving Peritoneal Dialysis (PD) or Hemodialysis (HD). The 24-week study is divided into two 12-week dosing periods (Dosing Period 1 followed by Dosing Period 2).

From ClinicalTrials.gov, last updated 2026-06-15. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $107,810 in research payments for this study in 2025 (26 payments).

Products named: Zemplar

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.