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Calcimimetics in Hypophosphatemic Rickets (CHR)

Primary Purpose

Familial Hypophosphatemic Rickets

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cinacalcet
Sponsored by
Children's Mercy Hospital Kansas City
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Familial Hypophosphatemic Rickets focused on measuring Familial hypophosphatemic rickets, Cinacalcet, hyperparathyroidism

Eligibility Criteria

5 Years - 21 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Patients with XLH
  2. Age 5-21 years old
  3. From the Renal and Endocrinology Clinics who have been in a stable clinical, biochemical and radiological condition for the preceding 9 months
  4. Who have not received Cinacalcet before

Exclusion Criteria:

  1. Treatment with growth hormone
  2. Inability to swallow pills.
  3. An orthopedic surgery or braces in the past 9 months, or scheduled within 9 months of start.
  4. Pregnancy
  5. History of seizure disorder
  6. Abnormal liver functions (which may change the drug's AUC)

Sites / Locations

  • Children's Mercy Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Cinacalcet

Arm Description

Stable patients with XLH already treated with Phosphate and calcitriol will add Cinacalcet to their treatment regimen. Sequential monitoring of blood and urine biochemical variables will follow, based on which adjustments to the doses of the 3 medications will be done.

Outcomes

Primary Outcome Measures

doses of phosphate and calcitriol required to sustain goals of blood and urine chemistries

Secondary Outcome Measures

Full Information

First Posted
February 12, 2009
Last Updated
December 15, 2020
Sponsor
Children's Mercy Hospital Kansas City
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1. Study Identification

Unique Protocol Identification Number
NCT00844740
Brief Title
Calcimimetics in Hypophosphatemic Rickets
Acronym
CHR
Official Title
Effect of Cinacalcet on the Long-term Treatment of Familial Hypophosphatemic Rickets
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Withdrawn
Study Start Date
March 1, 2009 (Anticipated)
Primary Completion Date
March 1, 2012 (Anticipated)
Study Completion Date
March 1, 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Mercy Hospital Kansas City

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Currently, large oral doses of phosphate and 1,25(OH)2D (calcitriol) are the standard treatment of patients with familial hypophosphatemic rickets (XLH). While this therapy is effective in healing the rickets, it is often limited by development of complications due to the high dose of medications required to achieve cure. Among them are the development of calcifications in the kidneys and secondary hyperparathyroidism (HPT) which in some patients may cause complications like high blood calcium level, high blood pressure and damage to the kidney. A drug to treat secondary hyperparathyroidism was just developed. In a short term study we found that it might help the treatment of XLH, by allowing the use of lower doses of the both phosphate and calcitriol. In the present study we will learn if indeed the addition of this new medicine (Cinacalcet) to the long-term treatment will allow the use of lower doses of both phosphate and calcitriol and consequently lower the risk of complications.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Familial Hypophosphatemic Rickets
Keywords
Familial hypophosphatemic rickets, Cinacalcet, hyperparathyroidism

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cinacalcet
Arm Type
Experimental
Arm Description
Stable patients with XLH already treated with Phosphate and calcitriol will add Cinacalcet to their treatment regimen. Sequential monitoring of blood and urine biochemical variables will follow, based on which adjustments to the doses of the 3 medications will be done.
Intervention Type
Drug
Intervention Name(s)
Cinacalcet
Other Intervention Name(s)
Sensipar
Intervention Description
Stable patients with XLH already treated with Phosphate and calcitriol will add Cinacalcet to their treatment regimen. Sequential monitoring of blood nand urine biochemical variables will follow, based on which adjustments to the doses of the 3 medications will be done.
Primary Outcome Measure Information:
Title
doses of phosphate and calcitriol required to sustain goals of blood and urine chemistries
Time Frame
9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients with XLH Age 5-21 years old From the Renal and Endocrinology Clinics who have been in a stable clinical, biochemical and radiological condition for the preceding 9 months Who have not received Cinacalcet before Exclusion Criteria: Treatment with growth hormone Inability to swallow pills. An orthopedic surgery or braces in the past 9 months, or scheduled within 9 months of start. Pregnancy History of seizure disorder Abnormal liver functions (which may change the drug's AUC)
Facility Information:
Facility Name
Children's Mercy Hospital
City
Kansas City
State/Province
Missouri
ZIP/Postal Code
64108
Country
United States

12. IPD Sharing Statement

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Calcimimetics in Hypophosphatemic Rickets

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