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CompletedNCT04184661HYPO-CLASTEUpdated Oct 6, 2022

Burosumab and 1-25 (OH) Vitamin D on Human Osteoclasts

An observational study in Hypophosphatemic Rickets, sponsored by Hospices Civils de Lyon. Completed at 3 sites in France. Open to participants aged 2 Years and older. Per ClinicalTrials.gov, last updated 2022-10-06.

Sponsored by Hospices Civils de Lyon · Observational

Study type
Observational
Model
Case-control
Time perspective
Prospective
Enrollment
52
Ages
2 Years and older
Sex
All
01

Study summary

Fibroblast growth factor 23 (FGF23) is the cornerstone of phosphate / calcium / vitamin D metabolism: it is synthesized mainly by osteocytes and acts as a Phosphating agent, inhibitor of dihydroxyvitamin D, and inhibitor of synthesis and secretion of Parathyroid hormone (PTH) in most tissues.

The specific role of FGF23 on bone has yet to be demonstrated. In some diseases such as hypophosphatemic rickets (HR), the direct role of FGF23 on bone has not yet been studied to our knowledge, whereas these genetic hypophosphatemias are secondary to overexpression of FGF23, whether an activating mutation of FGF23 or inhibitory mutations of its inhibitors (Dentin matrix acidic phosphoprotein 1 (DMP1) and Phosphate-regulating neutral endopeptidase, X-linked (PHEX)). However, patients with X-linked hypophosphatemic rickets (XLH) have higher circulating FGF23 levels than healthy controls and these levels are higher in treated patients.

Management of XLH consists primarily of correcting the native vitamin D defect by prescribing active vitamin D analogs as well as phosphate supplementation to improve bone mineralization and decrease dental complications, growth, and bone deformities. Recently, a new therapeutic option has been developed for XLH, burosumab, a human monoclonal antibody that binds and inhibits FGF23 activity. The use of burosumab is currently authorized in France in some pediatric patients with severe forms of XLH.

Independently of the indirect bone effects of phosphate correction and vitamin D levels, the direct role of burosumab on bone cells has never been studied. The objective of this project is to study the osteoclastic biology of patients with HR compared to control patients, and to evaluate the direct impact of the treatments used in this pathology on human osteoclasts.

02

Conditions studied

  • Hypophosphatemic Rickets
03

In context

Rickets, Hypophosphatemic

10 studies on the registry are indexed under Rickets, Hypophosphatemic; none are open to participants now.

Browse Rickets, Hypophosphatemic studies →

Lead sponsor

Hospices Civils de Lyon is the lead sponsor of 1,866 studies on the registry; 448 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
2 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patients with hypophosphatemic rickets and controls patients without hypophosphatemic rickets

Eligibility criteria

hypophosphatemic rickets patients:

Inclusion Criteria:

  • children from 2 yars-old to 18 years old and adults
  • patients with HR followed in the center of calcium and phosphorus metabolism rare diseases in Lyon-
  • Patients and parent / holder of parental authority who have been informed of the study and do not object to participate

Exclusion Criteria:

  • Patient being treated with oral or having received more than 3 months of corticosteroid treatment before surgery.
  • Patients under tutorship or curatorship
  • Pregnant and / or breastfeeding woman
  • Patient deprived of liberty

Controls patients:

Inclusion Criteria:

  • children from 2 years-old to 18 years old and adults
  • patients with normal renal function (Schwartz (GFR) >90 ml/min/1.73m²)
  • Patients and parent / holder of parental authority who have been informed of the study and do not object to participate

Exclusion Criteria:

  • Patient being treated with oral corticosteroid or having received more than 3 months of corticosteroid treatment before surgery.
  • Patients under tutorship or curatorship
  • Pregnant and / or breastfeeding woman
  • Patient deprived of liberty
  • Patient treated with drugs
  • Patient with inflammatory disease
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

05

Study design

Observational model
Case-control
Time perspective
Prospective
Enrollment
52 participants (actual)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • hypophosphatemic rickets patients

    30 hypophosphatemic rickets patients older than 2 years will be included in this study

    Other: blood sample

  • controls patients

    10 controls patients from pediatric nephrology unit without hypophosphatemic rickets, older than 2 years will be included in this study

    Other: blood sample

Interventions

  • Otherblood sample

    25 mL blood sample will be collected on citrate tubes for osteoclastic analysis.

06

What researchers measure

Primary outcomes

  1. number of osteoclastic cells obtained after at the end of differentiation

    The analysis of osteoclastic differentiation will be obtained from the bone cells from patients with burosumab and/or 1-25 (OH) vitamin D

    Time frame: 1 day

07

Study locations

3 sites
  • Hôpital Femme mère enfant
    Bron, 69677, France
  • Hôpital Edouard Herriot
    Lyon, France
  • Hôpital Bicêtre Paris Saclay
    Paris, France
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Jan 2021 to primary completion in Oct 2021, 9 months.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 28, 2019
First posted
Dec 3, 2019
StartActual
Jan 20, 2021
Primary completionActual
Oct 27, 2021
CompletionActual
Oct 27, 2021
Last update
Oct 6, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Oct 6, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04184661
Responsible party
Sponsor
First posted
Dec 3, 2019
Start date
Jan 20, 2021
Primary completion
Oct 27, 2021
Completion
Oct 27, 2021
Last update
Oct 6, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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