Category Filter
- Advanced Imaging
- Autism Spectrum Mandate
- Behavioral Health
- Blue Advantage Policies
- Chronic Condition Management
- Genetic Testing
- HelpScript Program
- Hemophilia Drugs
- Medical Policies
- Pre-Service Review (Predetermination/Precertification)
- Provider-Administered Drug Policies
- Radiation Therapy
- Self-Administered Drug Policies
- Transgender Services
Asset Publisher
Phenylketonuria Prior Authorization Program Summary
Policy Number: PH-1067
This prior authorization program applies to Blue Partner, Commercial, GenPlus, NetResults A series, SourceRx and Health Insurance Marketplace formularies.
POLICY REVIEW CYCLE
Effective Date |
Date of Origin |
1/1/2024 |
|
FDA APPROVED INDICATIONS AND DOSAGE
Agent(s) |
FDA Indication(s) |
Notes |
Ref# |
Kuvan® (sapropterin)* Tablet Oral solution |
Reduce blood phenylalanine (Phe) levels in adult and pediatric patients one month of age and older with hyperphenylalaninemia (HPA) due to tetrahydrobiopterin-(BH4-) responsive phenylketonuria (PKU). To be used in conjunction with a Phe-restricted diet. |
* generic available |
1 |
Palynziq® (pegvaliase-pqpz) Subcutaneous injection |
To reduce blood phenylalanine concentrations in adult patients with phenylketonuria (PKU) who have uncontrolled blood phenylalanine concentrations greater than 600 micromol/L on existing management. Existing management options include prior or current restriction of dietary phenylalanine and protein intake, and/or prior treatment with sapropterin dihydrochloride. |
|
2 |
See package insert for FDA prescribing information: https://dailymed.nlm.nih.gov/dailymed/index.cfm
CLINICAL RATIONALE
Phenylketonuria |
Phenylketonuria (PKU), also known as phenylalanine hydroxylase (PAH) deficiency, is a rare autosomal recessive error of phenylalanine (Phe) metabolism caused by variants in the gene encoding PAH. PAH deficiency leads to accumulation of Phe in the blood and brain. Untreated, PKU is characterized by irreversible intellectual disability, microcephaly, motor deficits, eczematous rash, autism, seizures, developmental problems, aberrant behavior, and psychiatric symptoms. Since the initiation of newborn screening, almost all cases of PAH deficiency are diagnosed following a positive newborn screening test.(3,4,5) Treatment is recommended to be taken as early as possible, preferably within the first week of life with a goal of having blood Phe in the treatment range within the first 2 weeks of life.(4,5) Dietary therapy, involving dietary Phe restriction and supplementation with reduced or Phe-free amino acid mixtures (medical foods, formulas), is the mainstay of therapy and effective in preventing severe mental retardation association with untreated classical PAH deficiency.(3,4,5) There is not clear consensus regarding clinical outcomes in treating patients with Phe blood concentrations between 360 and 600 micromol/L, however given the risk for neurocognitive consequences many treatment centers initiate treatment at a Phe level of 360 micromol/L or higher in patients during the first 12 years of life.(3,4) Guidelines recommend patients less than 12 years of age should have target blood Phe between 120 and 360 micromol/L. Patients age 12 or greater with untreated Phe blood concentration greater than 600 micromol/L should be treated. For patients 12 years of age and older, target Phe levels should be 120 to 600 micromol/L.(3) Pregnancy presents a problem in women with PAH deficiency, as high levels of Phe are toxic to the brain of the developing fetus and along with other teratogenic effects, results in a defined maternal PKU syndrome. Treatment should be considered for women prior to conception with blood Phe greater than 360 micromol/L due to risks of maternal PKU.(3,4,5) Treatment for life is recommended, even though it is acknowledged that dietary management is associated with significant patient burden.(3,4,5) Over time, subtle intellectual and neuropsychiatric issues may manifest even with treatment.(4) In addition, patients treated from the early weeks of life with initial good metabolic control, but who lose control later in childhood or adult life, may experience both reversible and irreversible neuropsychiatric consequences. Even severely intellectually disabled adults with late-diagnosed PAH deficiency show improvements in challenging behavior with lowering of blood Phe levels.(3,4) Sapropterin is a synthetic form of naturally occurring cofactor, tetrahydrobiopterin. Some patients with PAH deficiency who have some residual enzyme activity respond to administration of sapropterin with an increase in the metabolism of Phe to tyrosine.(3) Approximately 25-50% of patients with PAH deficiency are sapropterin responsive. A significant decline in blood Phe is expected in responders with the assumption that diet remains stable with sapropterin therapy. Most sapropterin-responsive patients have a rapid decline in blood Phe level, but occasionally a delay of 2-4 weeks is seen.(4) Clinical judgment is required to determine what constitutes as a significant or beneficial blood Phe decline in an individual patient, but 30% is often cited as evidence of effective Phe reduction since clinical trials for sapropterin identified responders as greater than or equal to 30% decrease in blood Phe from baseline.(1,4) Pegvaliase-pqpz is a phenylalanine-metabolizing enzyme. Patients should discontinue pegvaliase-pqpz if they have not achieved an adequate response (i.e., blood phenylalanine concentration less than or equal to 600 micromol/L) after 16 weeks of continuous treatment with the maximum dosage of 60 mg once daily.(2) |
Safety |
Kuvan (sapropterin) does not have any contraindications.(1) Palynziq (pegvaliase-pqpz) does not have any contraindications but does carry a boxed warning. Anaphylaxis has been reported after administration of pegvaliase-pqpz and may occur at any time during treatment. Auto-injectable epinephrine is prescribed to all patients treated with pegvaliase-pqpz, and the patient (and observer, if applicable) are instructed in recognizing signs and symptoms of anaphylaxis. Due to this, pegvaliase-pqpz is available only through a restricted program called Palynziq REMS.(2) |
REFERENCES
Number |
Reference |
1 |
Kuvan prescribing information. BioMarin Pharmaceutical Inc. February 2021. |
2 |
Palynziq prescribing information. BioMarin Pharmaceutical Inc. November 2020. |
3 |
van Wegberg AMJ, MacDonald A, Ahring K, et al. The Complete European Guidelines on Phenylketonuria: Diagnosis and Treatment. Orphanet J Rare Dis. 2017;12(1):162. |
4 |
Vockley J, Andersson HC, Antshel KM, et al. American College of Medical Genetics and Genomics (ACMG) for Phenylalanine Hydroxylase Deficiency: Diagnosis and Management Guideline. Genet Medicine. 2014;16(2):188–200. |
5 |
Genetic Metabolic Dietitians International (GMDI) and Southeast Regional Genetics Network (SERN): PKU Nutrition Management Guidelines. March 2022 v.2.5 [Updated June 2022]. Available at: https://managementguidelines.net/guidelines.php/136/overview/0/0/PKU%20Nutrition%20Guidelines/Version%202.5/Overview. |
POLICY AGENT SUMMARY PRIOR AUTHORIZATION
Target Brand Agent(s) |
Target Generic Agent(s) |
Strength |
Targeted MSC |
Available MSC |
Final Age Limit |
Preferred Status |
|
||||||
Palynziq |
pegvaliase-pqpz subcutaneous soln pref syringe |
10 MG/0.5ML ; 2.5 MG/0.5ML ; 20 MG/ML |
M ; N ; O ; Y |
N |
|
|
Javygtor ; Kuvan |
sapropterin dihydrochloride powder packet ; sapropterin dihydrochloride tab |
100 ; 100 MG ; 500 ; 500 MG |
M ; N ; O ; Y |
O ; Y |
|
|
CLIENT SUMMARY – PRIOR AUTHORIZATION
Target Brand Agent Name(s) |
Target Generic Agent Name(s) |
Strength |
Client Formulary |
Javygtor ; Kuvan |
sapropterin dihydrochloride powder packet ; sapropterin dihydrochloride tab |
100 ; 100 MG ; 500 ; 500 MG |
Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx |
Palynziq |
pegvaliase-pqpz subcutaneous soln pref syringe |
10 MG/0.5ML ; 2.5 MG/0.5ML ; 20 MG/ML |
Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx |
PRIOR AUTHORIZATION CLINICAL CRITERIA FOR APPROVAL
Module |
Clinical Criteria for Approval |
|
INITIAL EVALUATION Target Agent(s) will be approved when ALL of the following are met:
Length of Approval: Kuvan (sapropterin): Approve for 2 months if initial dose is 5 mg/kg/day to less than 20 mg/kg/day, and for 1 month if initial dose is 20 mg/kg/day Palynziq (pegvaliase-pqpz): 9 months *Step therapy requirement may not apply if a prior health plan paid for the medication - documentation of a paid claim may be required.
RENEWAL EVALUATION Target Agent(s) will be approved when ALL of the following are met:
Length of Approval: 12 months |
This pharmacy policy is not an authorization, certification, explanation of benefits or a contract. Eligibility and benefits are determined on a case-by-case basis according to the terms of the member’s plan in effect as of the date services are rendered. All pharmacy policies are based on (i) information in FDA approved package inserts (and black box warning, alerts, or other information disseminated by the FDA as applicable); (ii) research of current medical and pharmacy literature; and/or (iii) review of common medical practices in the treatment and diagnosis of disease as of the date hereof. Physicians and other providers are solely responsible for all aspects of medical care and treatment, including the type, quality, and levels of care and treatment.
The purpose of Blue Cross and Blue Shield of Alabama’s pharmacy policies are to provide a guide to coverage. Pharmacy policies are not intended to dictate to physicians how to practice medicine. Physicians should exercise their medical judgment in providing the care they feel is most appropriate for their patients.
Neither this policy, nor the successful adjudication of a pharmacy claim, is guarantee of payment.
BCBSAL _ Commercial _ CSReg _ Phenylketonuria _PA _ProgSum_ 1/1/2024