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CompletedNCT00830674Updated Jun 17, 2024

A Study of KRN23 in X-linked Hypophosphatemia

A Phase 1 interventional study of Placebo and KRN23 in X-linked Hypophosphatemia, sponsored by Kyowa Kirin Co., Ltd.. Completed at 4 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-06-17.

Sponsored by Kyowa Kirin Co., Ltd. · Phase 1, Interventional, and Treatment

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Phase
Phase 1
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 18 studies testing burosumab in Familial Hypophosphatemic Rickets — none open to participants now, none under way, none of them phase 3. burosumab · Familial Hypophosphatemic Rickets.

Enrollment
5th of 18
42 · median 26
Started
2008
the only one that year
Phase 1
2 of 18
none open now
Registered
1st of 18
by date
Lead sponsor
7 of 18
Kyowa Kirin Co., Ltd.

Among the 18 studies testing burosumab in Familial Hypophosphatemic Rickets, this one is the 5th largest by enrollment, is the only one that started in 2008, is one of 2 in phase 1, and was the 1st registered.

Familial Hypophosphatemic Rickets

49 studies on the registry are indexed under Familial Hypophosphatemic Rickets; 8 are open to participants now.

Browse Familial Hypophosphatemic Rickets studies →

Open to participants now

None of the 18 studies testing burosumab in Familial Hypophosphatemic Rickets is open now. The open studies under Familial Hypophosphatemic Rickets, anywhere →

About burosumab

burosumab: first FDA approval 2018 (CRYSVITA), first EMA approval 2018. What it is approved for, and how studies give it, is on its page →

Who these studies take

Of the 4 Familial Hypophosphatemic Rickets studies recruiting now, 2 set no upper age limit and 2 stop at 75 or younger; 3 take children under 18; 1 takes healthy volunteers.

This study: 18 Years and older · all sexes · no healthy volunteers.

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Download CSVNarrow it in search →With an account: the 18 studies testing burosumab in Familial Hypophosphatemic Rickets as a file.
02

Study summary

The primary objective of this study is to assess the safety and tolerability of KRN23 after a single intravenous (IV) and subcutaneous (SC) administration in XLH patients.

03

Conditions studied

  • X-linked Hypophosphatemia

Keywords

  • XLH
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. 18 years or older
  2. Clinical diagnosis of XLH
  3. TmP/ is less than 2.0 mg/dL
  4. GFR is 60 mL/min or above

Exclusion criteria

Exclusion Criteria:

  1. Have any sign of active infectious disease or have had an infection requiring treatment with antibiotics within three weeks prior to screening
  2. History of known immunodeficiency
  3. Lactating females, female patients who are pregnant or planning to become pregnant during the study
  4. Use of a pharmacologic vitamin D metabolite or its analog, phosphate, calcimimetics, and ingestion of aluminum hydroxide antacids within 10 days prior to screening and dosing
  5. Use of any supplement contained phosphate, calcium and/or vitamin D within 10 days prior to screening and dosing
  6. Receipt of live (attenuated) vaccine within 3-months prior to screening
  7. Have any condition which, in the opinion of the Investigator, could present a concern for either patient safety or difficulty with data interpretation
Terms in these criteria, in plain language(1)

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.

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.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
42 participants (actual)

Study arms

  • Experimental
    KRN23

    Single IV or SC administration on day 1

    Drug: KRN23

  • Placebo comparator
    Placebo

    Single IV or SC administration on day 1

    Drug: Placebo

Interventions

  • DrugPlacebo

    single dose IV or SC administration

  • DrugKRN23

    Single IV administration on day 1: 0.003, 0.01, 0.03, 0.1 and 0.3 mg/kg and Single SC administration on day 1: 0.1, 0.3, 0.6 and 1.0 mg/kg

06

What researchers measure

Primary outcomes

  1. Safety and tolerability

    AEs, etc

    Time frame: Up to 7 weeks after dosing (maximally 11 weeks)

Secondary outcomes

  1. Effect to pharmacodynamic parameter

    Change in Serum Phosphate

    Time frame: Up to 7 weeks after dosing (maximally 11 weeks)

07

Study locations

4 sites
  • Yale University School of Medicine
    New Haven, Connecticut 06510, United States
  • General Clinical Research Center, Indiana University School of Medicine
    Indianapolis, Indiana 46202-5250, United States
  • Duke Clinical Research Unit
    Durham, North Carolina 27710, United States
  • University of Texas Health Science Center at Houston
    Houston, Texas 77030, United States
08

References and documents

Publications

  • Carpenter TO, Imel EA, Ruppe MD, Weber TJ, Klausner MA, Wooddell MM, Kawakami T, Ito T, Zhang X, Humphrey J, Insogna KL, Peacock M. Randomized trial of the anti-FGF23 antibody KRN23 in X-linked hypophosphatemia. J Clin Invest. 2014 Apr;124(4):1587-97. doi: 10.1172/JCI72829. Epub 2014 Feb 24. PubMed 24569459 ↗
09

Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Dec 2008, a primary completion of Dec 2011 and a completion of May 2013. It does not say whether these dates are actual or estimated.

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

Registered
Jan 27, 2009
First posted
Jan 28, 2009
Start
Dec 2008
Primary completionActual
Dec 2011
CompletionActual
May 2013
Last update
Jun 17, 2024
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 Jun 17, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00830674
Collaborators
Kyowa Hakko Kirin Pharma, Inc.
Responsible party
Sponsor
First posted
Jan 28, 2009
Start date
Dec 2008
Primary completion
Dec 2011
Completion
May 2013
Last update
Jun 17, 2024

Study contacts

Thomas O. Carpenter, M.D.
principal investigator · Yale University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: Burosumab

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