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Accession Number
Approved, Investigational
Biologic Classification
Protein Based Therapies
Monoclonal antibody (mAb)

Burosumab (KRN23) is an entirely human monoclonal IgG1 antibody that binds excess fibroblast growth factor 23 (FGF23) and has been successfully tested in clinical trials in children with X-linked hypophosphatemic rickets 1.

The U.S. Food and Drug Administration approved Crysvita (burosumab) in April 2018. This is the first drug approved to treat adults and children ages 1 year and older with X-linked hypophosphatemia (XLH), which is a rare, inherited form of rickets. X-linked hypophosphatemia causes low circulating levels of phosphorus in the blood. It causes impaired bone growth and development in children and adolescents and issues with bone mineralization throughout a patient’s life 3.

XLH is a serious disease which affects about 3,000 children and 12,000 adults in the United States. Most children with XLH suffer from bowed or bent legs, short stature, bone pain and severe dental pain. Some adults with this condition suffer from persistent, unrelenting discomfort and complications, such as joint pain, impaired mobility, tooth abscesses and hearing loss 3.

Protein chemical formula
Protein average weight
144100.0 Da
> Burosumab Heavy Chain Sequence
> Burosumab Light Chain Sequence
Download FASTA Format
  • Burosumab (genetical recombination)
  • burosumab-twza
External IDs
KRN-23 / KRN23
Prescription Products
NameDosageStrengthRouteLabellerMarketing StartMarketing End
CrysvitaSolution10 mgSubcutaneousKyowa Kirin Limited2019-01-28Not applicableCanada
CrysvitaInjection20 mg/1mLSubcutaneousUltragenyx Pharmaceutical Inc.2018-04-18Not applicableUs
CrysvitaInjection30 mg/1mLSubcutaneousUltragenyx Pharmaceutical Inc.2018-04-18Not applicableUs
CrysvitaSolution30 mgSubcutaneousKyowa Kirin Limited2019-01-28Not applicableCanada
CrysvitaInjection10 mg/1mLSubcutaneousUltragenyx Pharmaceutical Inc.2018-04-18Not applicableUs
CrysvitaSolution20 mgSubcutaneousKyowa Kirin Limited2019-01-28Not applicableCanada
Additional Data Available
  • Application Number
    Application Number

    A unique ID assigned by the FDA when a product is submitted for approval by the labeller.

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  • Product Code
    Product Code

    A governmentally-recognized ID which uniquely identifies the product within its regulatory market.

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CAS number



This drug is indicated for the treatment of X-linked hypophosphatemia with radiological evidence of bone disease in children of 1 year of age and older and adolescents with growing skeletons 4.

Associated Conditions

This drug has the ability to reduce the loss of phosphate, to improve pathologically low serum phosphate concentrations and other metabolic changes, as well as to reduce the severity of rickets as seen radiographically 5. In summary, this drug works to support of bone mineralization 4.

Mechanism of action

Burosumab is a recombinant human monoclonal antibody (IgG1) that both binds to and inhibits the actions of fibroblast growth factor 23 (FGF23). By inhibiting this growth factor, burosumab increases the tubular reabsorption of phosphate from the kidney and thus increases serum concentration of 1, 25 dihydroxy-Vitamin D 4. This form of vitamin D enhances intestinal absorption of phosphate and calcium, supporting bone mineralization 8.

AFibroblast growth factor 23
Additional Data Available
Adverse Effects

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Additional Data Available

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Blackbox Warnings

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Burosumab absorption after subcutaneous injection sites into to the blood circulation is nearly complete. Following the subcutaneous route of administration, the time to reach maximum serum concentrations (Tmax) of burosumab is estimated at 5-10 days. The peak serum concentration (Cmax) and area under the concentration-time curve (AUC) of serum burosumab is proportional to the dose, over the dose range of 0.1-2.0 mg/kg 4.

Volume of distribution

Burosumab is comprised solely of amino acids and carbohydrates as a native immunoglobulin and is not likeluy to be eliminated by hepatic metabolic mechanisms. The metabolism of burosumab and elimination are expected to follow the immunoglobulin clearance pathways, which results in its degradation to smaller peptides and amino acids 4.

Protein binding
Not Available

Burosumab is composed solely of amino acids and carbohydrates as a native immunoglobulin and is unlikely to be eliminated via hepatic metabolic mechanisms. Its metabolism and elimination are expected to follow the immunoglobulin clearance pathways, resulting in degradation to small peptides and individual amino acids 4.

Route of elimination

Because of its molecular size, burosumab is not likely to be directly excreted 4.

Half life

About 19 days 4.


The clearance of burosumab depends on weight and is estimated to be 0.290 L/day and 0.136 L/day in a typical adult (70 kg) and pediatric (30 kg) XLH patient, respectively 4.


The toxicity of Crysvita can be classified into several categories 4:

Ectopic mineralisation: Clinically manifested by nephrocalcinosis, has been seen in patients with XLH treated with oral phosphorous and vitamin D analogues. These drugs should be stopped at least 1 week before starting burosumab treatment 4.

Monitoring for signs and symptoms of nephrocalcinosis, e.g. by renal ultrasonography, is recommended at the beginning of treatment and at intervals of every 6 months for the first 12 months of treatment, and yearly thereafter. Regular monitoring of plasma alkaline phosphatases, Calcium, PTH, and creatinine is advised at 6 months intervals(every 3 months for children 1- 2 years) or as indicated 4.

Monitoring of urine calcium and phosphate is suggested every 3 months.


Fasting serum phosphate level must be followed due to the risk of hyperphosphatemia while taking this drug. To decrease the risk for ectopic mineralization, it is advised that fasting serum phosphate is aimed to be in the lower end of the normal reference range for any given age. Dose interruption and/or dose reduction may be required. Regular measurement of postprandial serum phosphate is advised 4.

Serum parathyroid hormone increases

Increases in serum parathyroid hormone have been measured in some XLH patients while undergoing treatment with burosumab. Regular measurement of serum parathyroid hormone is recommended 4.

Injection site reactions

Administration of burosumab, like other injections, can lead to local injection site reactions. Administration of this drug should cease in any patient experiencing severe injection site reactions and appropriate medical therapy administered 4.


Burosumab should be discontinued if serious hypersensitivity reactions occur and appropriate medical treatment should be provided 4.

Reproductive toxicity/pregnancy

There are no or limited amount of data available from the use of burosumab in pregnant women. Studies in animals have demonstrated reproductive toxicity. Burosumab use is not advised during pregnancy and in women of childbearing potential/age currently not using contraception 4.

Affected organisms
  • Humans and other mammals
Not Available
Pharmacogenomic Effects/ADRs
Not Available


Drug Interactions
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a healthcare provider immediately. The absence of an interaction does not necessarily mean no interactions exist.
AbciximabThe risk or severity of adverse effects can be increased when Abciximab is combined with Burosumab.
AbituzumabThe risk or severity of adverse effects can be increased when Abituzumab is combined with Burosumab.
AbrilumabThe risk or severity of adverse effects can be increased when Burosumab is combined with Abrilumab.
AdalimumabThe risk or severity of adverse effects can be increased when Adalimumab is combined with Burosumab.
AdecatumumabThe risk or severity of adverse effects can be increased when Adecatumumab is combined with Burosumab.
AducanumabThe risk or severity of adverse effects can be increased when Aducanumab is combined with Burosumab.
AfelimomabThe risk or severity of adverse effects can be increased when Afelimomab is combined with Burosumab.
AlemtuzumabThe risk or severity of adverse effects can be increased when Alemtuzumab is combined with Burosumab.
AlirocumabThe risk or severity of adverse effects can be increased when Alirocumab is combined with Burosumab.
AmatuximabThe risk or severity of adverse effects can be increased when Amatuximab is combined with Burosumab.
Additional Data Available
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Food Interactions
Not Available


General References
  1. Kutilek S: Burosumab: A new drug to treat hypophosphatemic rickets. Sudan J Paediatr. 2017;17(2):71-73. doi: 10.24911/SJP.2017.2.11. [PubMed:29545670]
  2. Kinoshita Y, Fukumoto S: X-linked hypophosphatemia and FGF23-related hypophosphatemic diseases -Prospect for new treatment. Endocr Rev. 2018 Jan 26. pii: 4825438. doi: 10.1210/er.2017-00220. [PubMed:29381780]
  3. FDA approves first therapy for rare inherited form of rickets, x-linked hypophosphatemia [Link]
  4. Crysvita Drug Label [Link]
  5. Burosumab for a rare bone disease [Link]
  6. DRUG: Burosumab [Link]
  7. NHS document [Link]
  8. Burosumab for XLH [Link]
External Links
ATC Codes
M05BX05 — Burosumab
AHFS Codes
  • 40:92.00 — Electrolytic, Caloric and Water Balance Agents, Miscellanous

Clinical Trials

Clinical Trials
0Not Yet RecruitingSupportive CareCutaneous Skeletal Hypophosphatemia Syndrome (CSHS) / Epidermal Nevus Syndrome1
1CompletedTreatmentX-Linked Hypophosphatemia1
1CompletedTreatmentX-linked Hypophosphatemic Rickets/Osteomalacia1
1, 2CompletedTreatmentX-Linked Hypophosphatemia2
1, 2Not Yet RecruitingTreatmentX-linked Hypophosphatemia (XLH)1
2Active Not RecruitingTreatmentEpidermal Nevus Syndrome (ENS) / Tumor Induced Osteomalacia (TIO)1
2Active Not RecruitingTreatmentTumor-Induced Osteomalacia or Epidermal Nevus Syndrome1
2CompletedTreatmentX-Linked Hypophosphatemia3
3Active Not RecruitingTreatmentX-linked Hypophosphatemic Rickets/Osteomalacia1
3CompletedTreatmentHypophosphatemia / Hypophosphatemic Rickets / Pain, Chronic1
3CompletedTreatmentX-Linked Hypophosphatemia3
3RecruitingTreatmentX-Linked Hypophosphatemia1
4RecruitingOtherX-Linked Hypophosphatemia1
Not AvailableAvailableNot AvailableTumor-Induced Osteomalacia / X-Linked Hypophosphatemia1


Not Available
Not Available
Dosage forms
InjectionSubcutaneous10 mg/1mL
InjectionSubcutaneous20 mg/1mL
InjectionSubcutaneous30 mg/1mL
SolutionSubcutaneous10 mg
SolutionSubcutaneous20 mg
SolutionSubcutaneous30 mg
Not Available
Not Available


Experimental Properties
Not Available


Not Available
Organic Compounds
Super Class
Organic Acids
Carboxylic Acids and Derivatives
Sub Class
Amino Acids, Peptides, and Analogues
Direct Parent
Alternative Parents
Not Available
Not Available
Molecular Framework
Not Available
External Descriptors
Not Available


Pharmacological action
General Function
Not Available
Specific Function
Fibroblast growth factor receptor binding
Gene Name
Uniprot ID
Uniprot Name
Fibroblast growth factor 23
Molecular Weight
16440.335 Da
  1. Tardy B, Lecompte T, Boelhen F, Tardy-Poncet B, Elalamy I, Morange P, Gruel Y, Wolf M, Francois D, Racadot E, Camarasa P, Blouch MT, Nguyen F, Doubine S, Dutrillaux F, Alhenc-Gelas M, Martin-Toutain I, Bauters A, Ffrench P, de Maistre E, Grunebaum L, Mouton C, Huisse MG, Gouault-Heilmann M, Lucke V: Predictive factors for thrombosis and major bleeding in an observational study in 181 patients with heparin-induced thrombocytopenia treated with lepirudin. Blood. 2006 Sep 1;108(5):1492-6. Epub 2006 May 11. [PubMed:16690967]
  2. Kutilek S: Burosumab: A new drug to treat hypophosphatemic rickets. Sudan J Paediatr. 2017;17(2):71-73. doi: 10.24911/SJP.2017.2.11. [PubMed:29545670]
  3. Crysvita Drug Label [Link]
  4. Burosumab for XLH [Link]
  5. Burosumab for a rare bone disease [Link]
  6. DRUG: Burosumab [Link]

Drug created on April 18, 2018 09:27 / Updated on January 22, 2020 17:03