Ixinity (factor IX human recombinant, threonine 148)

Factor IX Intravenous Vial (Ea)

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Coagulation factor IX (recombinant) is a biosynthetic (recombinant DNA origin) preparation of blood coagulation factor IX.

Coagulation factor IX (recombinant) is a biosynthetic (recombinant DNA origin) preparation of blood coagulation factor IX. Coagulation factor IX is essential for blood clotting and maintenance of hemostasis. Patients with hemophilia B (Christmas disease) have deficient levels of endogenous factor IX, resulting in a hemorrhagic tendency and clinical manifestations such as bleeding into soft tissues, muscles, joints, and internal organs.

The clinical severity and frequency of bleeding in patients with hemophilia B correlate with the degree of deficiency of factor IX activity. Patients with mild hemophilia B generally have >5% of normal activity, those with moderate disease generally have 1-5% of normal activity, and those with severe disease have <1% of normal activity. Administration of coagulation factor IX (recombinant) to patients with hemophilia B results in increased plasma levels of factor IX and temporarily corrects the coagulation defect.

Treatment also may normalize the activated partial thromboplastin time (aPTT), which is typically prolonged in patients with hemophilia B.

Coagulation factor IX (recombinant) is produced by recombinant DNA technology in a mammalian cell expression system and undergoes several purification and virus-inactivating/removal processes (e.g., chromatography, nanofiltration, solvent/detergent). Coagulation factor IX (recombinant) is manufactured without animal or human components. Coagulation factor IX (recombinant) is similar in structure and function to plasma-derived factor IX, but is associated with a substantially reduced risk of transmission of bloodborne human viruses (e.g., human immunodeficiency virus (HIV), hepatitis A virus (HAV), hepatitis B virus (HBV), hepatitis C virus (HCV)).

In a pharmacokinetic study in previously treated patients (PTPs) receiving BeneFIX(R), in vivo recovery of factor IX following IV administration of 50 units/kg of the drug was approximately 28% lower than that achieved following administration of an equivalent dose of plasma-derived factor IX; the difference is presumably due to structural modifications of coagulation factor IX (recombinant). The half-life of BeneFIX(R) is 22.4 hours at baseline in PTPs and 23.8 hours at 6 months of receiving BeneFIX(R) 75 IU/kg. The half-life of BeneFIX(R) in infants (<=2 years of age), children aged 2 to <6 years, children aged 6 to <12 years, and adolescents and adults is 15.6, 16.7, 16.3, and 23.1 hours, respectively.

Following administration of a single dose of Rixubis(R) (71.3-79.4 units/kg) in PTPs >=12 years of age, half-life of the drug was approximately 26.7 hours. In pediatric patients, the half-life of Rixubis(R) (median dose of 75.3 units/kg) was approximately 23 hours for patients 6-11 years of age and approximately 28 hours for those <6 years of age. Results of single- and repeat-dose pharmacokinetic studies indicate that incremental recovery of Rixubis(R) remains consistent over time in both adult and pediatric populations.

Following administration of a single dose of 75 IU/kg Ixinity(R)in PTPs >=12 years of age, the terminal half-life was 24 hours; repeated dosing did not impact the pharmacokinetics of Ixinity(R). Following administration of 75 IU/kg of Ixinity(R) in PTPs <6 years of age, the terminal half-life was 15.9 hours; 16.8 hours in PTPs age 6 to <12 years. Decreased in vivo recovery has been observed in pediatric patients <=12 years of age compared with older individuals receiving coagulation factor IX (recombinant).

Coagulation factor IX (recombinant) readily diffuses through interstitial fluid and distributes in both intravascular and extravascular compartments. The drug circulates in plasma as a free molecule. Coagulation factor IX (recombinant) binds rapidly and reversibly to vascular endothelium.

Clearance of factor IX correlates with body weight and generally increases through adolescence, then stabilizes during adulthood.

USES: This medication is used to prevent or control bleeding in people with little or no factor IX (due to hemophilia B, Christmas disease). Factor IX is a protein (clotting factor) in the blood that works with other clotting factors to help the blood clot and stop bleeding. People with little or no factor IX are at risk for bleeding longer after an injury/surgery or bleeding suddenly (often in the joints/muscle) without an obvious cause.

This medication should not be used to treat other types of factor deficiencies (such as factors II, VII, VIII, X) or factor problems (such as inhibitor to factor XIII), to reverse the effects of "blood thinners" (such as warfarin), or to treat bleeding from low levels of liver-dependent clotting factors (due to liver problems).

Generic name: factor IX human recombinant, threonine 148
Pronunciation: (FACK-ter nine)
Drug class: Factor IX
Therapeutic class: Hematological Agents

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Ixinity:

  • Bleeding Episode In Hemophilia B
  • Bleeding Prevention In Hereditary Factor Ix Deficiency
  • Hemophilia B

Also known as: Christmas Disease, Factor Ix Deficiency, Factor Ix Dysfunction, Hemorrhaging In Hemophilia B, Plasma Thromboplastin Component Deficiency, Ptc Deficiency.

Dosing

No dosing information is available for this tab.

Drug interactions

No formal drug interaction studies have been performed to date with coagulation factor IX (recombinant).

Contraindications

*Life-threatening, immediate hypersensitivity (e.g., anaphylaxis) or known hypersensitivity reactions to coagulation factor IX (recombinant) or any ingredient in the formulation, including hamster protein.

*Rixubis(R) is also contraindicated in patients with disseminated intravascular coagulation (DIC) and in those with signs of fibrinolysis.

Adverse reactions

The most common adverse effects (>5%) reported in previously treated and previously untreated patients receiving BeneFIX(R) in clinical trials were fever, cough, headache, dizziness, nausea, injection site reaction, injection site pain, and skin-related hypersensitivity reactions such as rash and hives.

The most common adverse effects (>1%) reported in previously treated patients receiving Rixubis(R) in clinical trials were dysgeusia, pain in extremity, and positive test for furin antibody.

The most common adverse effect (>2%) reported in patients receiving Ixinity(R)in clinical trials was headache.

Precautions

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ICD codes

CodeTypeDescription
Bleeding episode in hemophilia B
D67ICD10CMHereditary factor IX deficiency
Bleeding prevention in hereditary factor IX deficiency
D67ICD10CMHereditary factor IX deficiency
Hemophilia B
D67ICD10CMHereditary factor IX deficiency

ICD code information from First Databank (FDB).

Formulary status

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Last reviewed · Source: First Databank (FDB) drug data