Xenpozyme (olipudase alfa-rpcp)

Metabolic Disease Enzyme Replacement - ASMD Intravenous Vial (EA)

Advertisement

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

Overview

Olipudase alfa-rpcp is a biosynthetic (recombinant DNA origin) form of human acid sphingomyelinase (ASM), a lysosomal enzyme that catalyzes hydrolysis of sphingomyelin.

Olipudase alfa-rpcp is a biosynthetic (recombinant DNA origin) form of human acid sphingomyelinase (ASM), a lysosomal enzyme that catalyzes hydrolysis of sphingomyelin. The drug is produced using a Chinese hamster ovary cell line.

Acid sphingomyelinase deficiency (ASMD) is a lysosomal storage disease that results from reduced activity of the enzyme ASM. In patients with this condition, olipudase alfa-rpcp provides an exogenous source of ASM for catabolism of sphingomyelin, which accumulates and causes manifestations of this disorder. Plasma ceramide levels, which are elevated in adult and pediatric patients with ASMD, showed a transient increase after each administration (post-infusion) of olipudase alfa-rpcp.

In the dose escalation phase, plasma ceramide levels were substantially increased compared to the baseline level. Plasma ceramide levels gradually decreased following repeated administration of olipudase alfa-rpcp and the preinfusion levels were generally lower than the baseline level during the maintenance phase of treatment. Plasma lysosphingomyelin levels, which are substantially elevated in the plasma of adult and pediatric patients with ASMD, decreased after repeated administration of olipudase alfa-rpcp.

In addition, liver sphingomyelin content, as assessed by histopathology, decreased from baseline to week 52 in adults with ASMD receiving olipudase alfa-rpcp compared to an increase in adult patients receiving placebo.

Peak plasma concentration and AUC of olipudase alfa-rpcp increase in a dose-proportional manner at doses ranging from 0.1 to 3 mg/kg. Olipudase alfa-rpcp is not expected to cross the blood-brain barrier or modulate the CNS manifestations of ASMD. The metabolic pathway of olipudase alfa-rpcp has not been characterized; however, the drug is expected to be metabolized into small peptides and amino acids via catabolic pathways.

The mean elimination half-life of olipudase alfa-rpcp in adults with ASMD ranges from 32 to 38 hours. Intact olipudase alfa-rpcp is unlikely to be filtered by the kidney or excreted in the urine; in addition, secretion into bile generally is not an important contributor to the elimination of therapeutic proteins such as olipudase alfa-rpcp.

USES: This medication is used to treat symptoms due to a certain inherited disorder (acid sphingomyelinase deficiency-ASMD). This condition causes buildup of a fatty substance called sphingomyelin in various parts of the body. Olipudase alfa is an enzyme that helps break down sphingomyelin.

It is not a cure for ASMD, but it can help decrease some symptoms caused by this disorder such as enlarged spleen and liver.

Generic name: olipudase alfa-rpcp
Pronunciation: (oh-LIP-ue-dase)
Drug class: Metabolic Disease Enzyme Replacement - ASMD
Therapeutic class: Metabolic Disease Enzyme Replacement Agents

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

Today’s intelligence on Xenpozyme

Intelligence content is not available yet.

Indications

The following indications are listed for Xenpozyme:

  • Non-Cns Manifestations Of Acid Sphingomyelinase Deficiency

Also known as: Non-Central Nervous System Manifestations Of Asmd.

Dosing

Dosage of olipudase alfa-rpcp in adults and pediatric patients is based on weight. Use actual body weight in patients with BMI <=30 kg/m2. In patients with BMI >30 kg/m2, use an adjusted body weight calculated by the following formula: adjusted body weight (kg) = (actual height in m)2 x 30.

Treatment with olipudase alfa-rpcp should always be initiated via a dose escalation regimen followed by a maintenance dose. The recommended initial dosage of olipudase alfa-rpcp in pediatric patients is 0.03 mg/kg, and the recommended maintenance dosage in pediatric patients is 3 mg/kg every 2 weeks. To reduce the risk of hypersensitivity and IARs or elevated transaminase levels, follow the recommended dosage titration schedule shown in Table 5.

Table 5. Olipudase Alfa-rpcp Dose Escalation Regimen for Pediatric Patients 0-17 Years of Age

Dose Number Dosage based on Actual or Adjusted Weight First dose (day 1/week 0) 0.03 mg/kg Second dose (week 2) 0.1 mg/kg Third dose (week 4) 0.3 mg/kg Fourth dose (week 6) 0.3 mg/kg Fifth dose (week 8) 0.6 mg/kg Sixth dose (week 10) 0.6 mg/kg Seventh dose (week 12) 1 mg/kg Eighth dose (week 14) 2 mg/kg Ninth dose (week 16) 3 mg/kg (recommended maintenance dose)

The recommended initial dosage of olipudase alfa-rpcp in adults is 0.1 mg/kg, and the recommended maintenance dosage in adults is 3 mg/kg every 2 weeks. To reduce the risk of hypersensitivity and IARs or elevated transaminase levels, follow the recommended dosage titration schedule shown in Table 6.

Table 6. Olipudase Alfa-rpcp Dose Escalation Regimen for Adults >=18 Years of Age

Dose Number Dosage based on Actual or Adjusted Weight First dose (day 1/week 0) 0.1 mg/kg Second dose (week 2) 0.3 mg/kg Third dose (week 4) 0.3 mg/kg Fourth dose (week 6) 0.6 mg/kg Fifth dose (week 8) 0.6 mg/kg Sixth dose (week 10) 1 mg/kg Seventh dose (week 12) 2 mg/kg Eighth dose (week 14) 3 mg/kg (recommended maintenance dose)

Drug interactions

Formal drug interaction studies with olipudase alfa-rpcp have not been performed to date. As a therapeutic protein, olipudase alfa is unlikely to be involved in cytochrome P-450 (CYP)- or transporter-mediated drug interactions.

Contraindications

*None.

Adverse reactions

Adverse effects reported in >=10% of adults receiving olipudase alfa-rpcp include headache, cough, diarrhea, hypotension, and ocular hyperemia.

Adverse effects reported in >=20% of pediatric patients receiving olipudase alfa-rpcp include pyrexia, cough, diarrhea, rhinitis, abdominal pain, vomiting, headache, urticaria, nausea, rash, arthralgia, pruritus, fatigue, and pharyngitis.

Precautions

No enhanced messaging available.

ICD codes

CodeTypeDescription
Non-CNS manifestations of acid sphingomyelinase deficiency
E75.240ICD10CMNiemann-pick disease type A
E75.241ICD10CMNiemann-pick disease type B
E75.244ICD10CMNiemann-pick disease type a/B

ICD code information from First Databank (FDB).

Formulary status

Search health-plan coverage for this drug by ZIP code.

Enter a ZIP code to view available health plans.

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