Palynziq (pegvaliase-pqpz)

Phenylketonuria (PKU) Treatment Agents Subcutaneous Syringe (Ml)

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

Overview

Pegvaliase-pqpz is a phenylalanine-metabolizing enzyme composed of biosynthetic (recombinant DNA origin) phenylalanine ammonia lyase (PAL) conjugated with polyethylene glycol (PEG).

Pegvaliase-pqpz is a phenylalanine-metabolizing enzyme composed of recombinant phenylalanine ammonia lyase (PAL) covalently bound to N-hydroxysuccinimide (NHS)-methoxypolyethylene glycol (PEG). Pegvaliase is used as an enzyme substitution therapy for the deficient phenylalanine hydroxylase enzyme in patients with phenylketonuria (PKU); the drug provides an alternate pathway for the breakdown of phenylalanine in such patients by converting phenylalanine to ammonia and trans-cinnamic acid, thereby reducing blood phenylalanine concentrations. Pegvaliase is prepared using recombinant DNA technology and a strain of Escherichia coli genetically modified to incorporate the PAL gene derived from the cyanobacterium Anabaena variabilis.

Pegylation of the PAL enzyme is intended to reduce immunogenicity and improve drug stability.

Pegvaliase reduces blood phenylalanine concentrations in patients with PKU. The pharmacodynamic effects of the drug are proportional to its plasma concentrations; as plasma concentrations decrease, the effects of pegvaliase on reduction of blood phenylalanine concentrations decrease. Peak plasma concentrations of pegvaliase are achieved in approximately 8 hours; however, the pharmacokinetics of the drug are highly variable due to individual immune response.

It is expected that the drug is metabolized via catabolic pathways and degraded into small peptides and amino acids; however, the route of elimination has not been studied. The mean elimination half-lives of pegvaliase in adult patients with PKU receiving 20 or 40 mg of the drug once daily are 47 or 60 hours, respectively.

USES: This medication is used by people with a certain inherited condition (phenylketonuria) to reduce high levels of a certain substance (phenylalanine) that builds up in the blood. Having high levels of phenylalanine in the blood may cause brain damage, heart problems, an abnormally small head size, and behavioral problems. Pegvaliase works by breaking down phenylalanine in the blood.

Along with using this medication, you should follow a special diet to control your blood phenylalanine levels. Ask your doctor for details.

Generic name: pegvaliase-pqpz
Pronunciation: (peg-VAL-i-ase)
Drug class: Phenylketonuria (PKU) Treatment Agents
Therapeutic class: Metabolic Modifiers

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Palynziq:

  • Phenylketonuria

Also known as: Classical Phenylketonuria.

Dosing

Dosage of pegvaliase should be individualized based on patient tolerability, blood phenylalanine concentrations, and dietary protein and phenylalanine intake. (See Dosage and Administration: General.)

The dosing regimen of pegvaliase for the treatment of phenylketonuria (PKU) consists of an induction, titration, and maintenance phase. The recommended initial adult dosage of pegvaliase-pqpz is 2.5 mg once weekly by subcutaneous injection for 4 weeks. The dosage should be increased slowly, as tolerated, over at least 5 weeks up to a target maintenance dosage of 20 mg once daily. The manufacturer provides a suggested schedule for dosage titration (see Table 1); however, dosage should be titrated based on individual response and tolerability. Patients who experience adverse effects may require slower titration to achieve their target maintenance dosage.

Table 1: Recommended Pegvaliase-pqpz Dosage Titration Regimen

Treatment Phase Dosage Duration Induction 2.5 mg once weekly 4 weeks Titration 2.5 mg twice weekly 1 week 10 mg once weekly 1 week 10 mg twice weekly 1 week 10 mg four times per 1 week week 10 mg once daily 1 week Maintenance 20 mg once daily 24 weeks

A therapeutic response may not be achieved until an effective maintenance dosage is attained; the lowest effective and tolerated maintenance dosage should be used. If a response is not obtained (i.e., blood phenylalanine concentrations do not decrease by at least 20% from baseline or remain elevated at a concentration greater than 600 mcmol/L) after 24 weeks of treatment with pegvaliase-pqpz 20 mg once daily, dosage may be increased to 40 mg once daily. If blood phenylalanine concentrations still do not decrease by at least 20% from baseline or remain elevated at a concentration greater than 600 mcmol/L after 16 weeks of treatment at the maximum dosage of 40 mg once daily, therapy should be discontinued.

If blood phenylalanine concentrations decrease to less than 30 mcmol/L during titration or maintenance therapy with pegvaliase, dosage may be reduced and/or dietary intake of protein and/or phenylalanine modified to maintain blood phenylalanine concentrations within a clinically acceptable range above 30 mcmol/L.

If anaphylaxis occurs and a decision is made to continue pegvaliase therapy, subsequent dosage should be titrated based on patient tolerability and therapeutic response. (See Anaphylaxis under Warnings/Precautions: Sensitivity Reactions, in Cautions.)

Drug interactions

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Contraindications

The manufacturer states there are no known contraindications to the use of pegvaliase-pqpz.

Adverse reactions

Adverse effects reported in at least 15% of patients receiving pegvaliase in clinical studies include injection site reactions, arthralgia (e.g., back pain, musculoskeletal pain, pain in extremities, neck pain), hypersensitivity reactions, pruritus, headache, generalized skin reactions lasting at least 14 days, nausea, vomiting, abdominal pain, diarrhea, oropharyngeal pain, cough, nasal congestion, fatigue, anxiety, dizziness, and alopecia.

Precautions

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ICD codes

CodeTypeDescription
Phenylketonuria
E70.0ICD10CMClassical phenylketonuria
E70.1ICD10CMOther hyperphenylalaninemias

ICD code information from First Databank (FDB).

Formulary status

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