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Phase 4 N=1 Treatment

A Trial to Assess the Safety and Efficacy of KRN23 in Epidermal Nevus Syndrome (ENS)

Epidermal Nevus Syndrome

Enrolled (actual)
1
Serious AEs
0.0%
Results posted
Oct 2022
Primary outcome: Primary: The Participant Will Achieve Normal Age-adjusted Phosphorous Levels as Tested by Fasting Serum Lab Values — 0.8; 1.2; 1.3; 1.1 mg/dl

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Crysvita (burosumab-twza) Treatment (Drug)
Age
Pediatric, Adult, Older Adult · 0+ yrs
Sex
Male
Sponsor
University of Alabama at Birmingham
Primary completion
Jul 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
The Participant Will Achieve Normal Age-adjusted Phosphorous Levels as Tested by Fasting Serum Lab Values
0.8; 1.2; 1.3; 1.1; 1.4; 1.7
SECONDARY
Participant Will Achieve Improving Vitamin D Levels as Measured by Serum Blood Tests.
15; 68; 105; 95; 115
SECONDARY
Participant Will Achieve Improving iPTH Levels as Measured by Serum Blood Tests.
334.5; 334.1; 317; 245.9; 330.4
SECONDARY
Participant Will Achieve Improving Calcium Levels as Measured by Serum Blood Tests.
10.5; 10.5; 11.2; 12; 13.4
SECONDARY
Participant Will Achieve Improvement of Underlying Skeletal Disease/Rickets as Assessed by Standard Radiographs.
-3.9
SECONDARY
Participant Will Achieve Improving Levels of Alkaline Phosphatase (ALP)
672.4; 468.3; 313; 287; 185.2

Summary

KRN23 is a fully human immunoglobulin monoclonal antibody (mAb) that binds to and inhibits the activity of fibroblast growth factor 23 (FGF23), leading to an increase in serum phosphorus levels. There are multiple disorders that result in unusually high circulating levels of FGF23, which in turn result in renal phosphate wasting and reduced levels of 1,25-dihydroxy vitamin D (1,25[OH]2D). Across these disorders the clinical symptoms are similar and often include osteomalacia (and, in children, rickets), muscle weakness, fatigue, bone pain, and fractures. KRN23 has been studied in one of these disorders, X-linked hypophosphatemia (XLH). In single- and repeat-dose clinical studies in subjects with XLH, subcutaneous (SC) administration of KRN23 consistently increased and sustained serum phosphorus levels and tubular reabsorption of phosphate (TRP) without a major impact on urine calcium levels or vitamin D metabolism. Positive results were also observed in a nonclinical pharmacology model of XLH. It is hypothesized that KRN23 may provide clinical benefit in this patient due to the common underlying feature in this patient and in patients with XLH - abnormally elevated FGF23 in the context of low age -adjusted serum phosphorous levels. The primary objective is to study the effect of KRN23 treatment on normalizing age-adjusted fasting serum phosphorous levels in a single pediatric patient with Epidermal Nevus Syndrome associated hypophosphatemic rickets.

Eligibility Criteria

Inclusion Criteria

  • Patient has confirmed ENS by physician diagnosis
  • Patient has confirmed FGF23 elevations in the context of low serum phosphorous 60 ml/min
  • Must be willing in the opinion of the investigator, to comply with study procedures and schedule
  • Provide written informed consent by a parent after

Exclusion Criteria

  • Patient should not use CRYSVITA with Oral phosphate or active Vitamin D analogs.
  • Patient and investigator should not initiate CRYSVITA if Phosphorus level is within or above normal.
  • CRYSVITA is contraindicated in patients with severe renal impairment or end stage renal disease because these conditions are associated with abnormal mineral metabolism.
  • The use or enrollment in studies using other investigational therapies including other monoclonal antibodies
  • Subject and their Parent not willing or not able to give written informed consent
  • In the Investigators opinion, the subject may not be able to meet all the requirements for study participation
  • Subject has a history of hypersensitivity to KRN23 excipients that in the opinion of the investigator, places the subject at an increased risk of adverse effects
  • Subject has a condition that in the opinion of the investigator could present a concern for subject safety or data interpretation.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04320316). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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