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Sucraid (sacrosidase) Prior Authorization with Quantity Limit Program Summary
Policy Number: PH-91144
This program applies to Blue Partner, Commercial, GenPlus, NetResults A series, SourceRx and Health Insurance Marketplace formularies.
POLICY REVIEW CYCLE
Effective Date |
Date of Origin |
01-01-2025 |
|
FDA LABELED INDICATIONS AND DOSAGE
Agent(s) |
FDA Indication(s) |
Notes |
Ref# |
Sucraid® |
Oral replacement therapy for treatment of genetically determined sucrase deficiency, which is part of congenital sucrase-isomaltase deficiency (CSID)
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|
1 |
See package insert for FDA prescribing information: https://dailymed.nlm.nih.gov/dailymed/index.cfm
CLINICAL RATIONALE
CSID |
Congenital sucrase-isomaltase deficiency (CSID) is a rare, chronic, autosomal recessive disorder characterized by the absence or deficiency of the enzymes sucrase and isomaltase.(3) Patients with CSID have two defective copies of the sucrase-isomaltase (SI) gene. The SI enzyme complex is naturally produced in the brush border lining of the small intestine and assists in the breakdown of certain sucrose and products of starch digestion (dextrins). When sucrase-isomaltase is absent or deficient, non-absorbed carbohydrates enter the distal small intestine and colon where they are fermented, leading to the excessive production of short-chain fatty acids and gases such as hydrogen, methane, and hydrogen sulfide. This in turn can lead to abdominal distension, cramping, pain, excessive flatulence, nausea/vomiting, and osmotic diarrhea. If left untreated, significant sucrase-isomaltase deficiency (SID) can result in inadequate growth and failure to thrive in children as well as weight loss in adults.(4) The gold standard for the diagnosis of CSID remains small intestinal biopsy specimens assayed for lactase, sucrase, isomaltase, and maltase activity. Criteria to make the diagnosis of CSID include normal small bowel morphology in the presence of markedly reduced or absent sucrase activity, isomaltase activity varying from zero to full activity, and reduced maltase activity. Lactase activity can be normal or reduced in children with a sucrase:lactase ratio of less than 1.0. Genetic sequencing of the SI gene can identify homozygous and compound heterozygous mutations responsible for CSID. A number of noninvasive diagnostic tests can also help establish the diagnosis, including the sucrose challenge test, lactose breath test, and hydrogen-methane breath test. However, many of these tests have limitations including false-positive results, false-negative results, and lack of validation data.(2) Previously, treatment of CSID has required lifelong adherence to a sucrose-free diet.(2-4) Data suggest that even after diagnosis and dietary treatment, major gastrointestinal symptoms persists, and there is a high frequency of decreased weight for height and age in these patients.(5) Treatment has improved considerably with the availability of enzyme replacement therapy (sacrosidase) which has allowed consumption of a more normal diet and decreased the high incidence of chronic gastrointestinal problems.(2-5) Access to a physician or dietician who is knowledgeable about CSID is essential for guiding patients and their families.(4) |
Safety |
Sucraid is contraindicated in patients known to be hypersensitive to yeast, yeast products, glycerin (glycerol), or papain.(1) |
REFERENCES
Number |
Reference |
1 |
Sucraid prescribing information. QOL Medical, LLC. December 2023. |
2 |
Treem WR. Clinical Aspects and Treatment of Congenital Sucrase‐Isomaltase Deficiency. Journal of Pediatric Gastroenterology and Nutrition. 2012;55(S2). doi:10.1097/01.mpg.0000421401.57633.90 |
3 |
Congenital Sucrase-Isomaltase Deficiency - Symptoms, Causes, treatment | NORD. National Organization for Rare Disorders. https://rarediseases.org/rare-diseases/disaccharide-intolerance-i/ |
4 |
Congenital Sucrase-Isomaltase Deficiency: What, when, and how? – Gastroenterology & Hepatology. https://www.gastroenterologyandhepatology.net/supplements/congenital-sucrase-isomaltase-deficiency-what-when-and-how/ |
5 |
Treem, W. R., McAdams, L., Stanford, L., Kastoff, G., Justinich, C., & Hyams, J. (1999). Sacrosidase therapy for Congenital Sucrase-Isomaltase Deficiency. Journal of Pediatric Gastroenterology and Nutrition, 28(2), 137–142. https://doi.org/10.1097/00005176-199902000-00008 |
POLICY AGENT SUMMARY PRIOR AUTHORIZATION
Target Brand Agent(s) |
Target Generic Agent(s) |
Strength |
Targeted MSC |
Available MSC |
Final Age Limit |
Preferred Status |
|
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Sucraid |
sacrosidase soln |
8500 UNIT/ML |
M ; N ; O ; Y |
N |
|
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POLICY AGENT SUMMARY QUANTITY LIMIT
Target Brand Agent Name(s) |
Target Generic Agent Name(s) |
Strength |
QL Amount |
Dose Form |
Day Supply |
Duration |
Addtl QL Info |
Allowed Exceptions |
Targeted NDCs When Exclusions Exist |
|
|||||||||
Sucraid |
sacrosidase soln |
8500 UNIT/ML |
300 |
mLs |
30 |
DAYS |
|
|
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CLIENT SUMMARY – PRIOR AUTHORIZATION
Target Brand Agent Name(s) |
Target Generic Agent Name(s) |
Strength |
Client Formulary |
Sucraid |
sacrosidase soln |
8500 UNIT/ML |
Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx |
CLIENT SUMMARY – QUANTITY LIMITS
Target Brand Agent Name(s) |
Target Generic Agent Name(s) |
Strength |
Client Formulary |
Sucraid |
sacrosidase soln |
8500 UNIT/ML |
Blue Partner ; Commercial ; GenPlus ; Health Insurance Marketplace ; NetResults A Series ; SourceRx |
PRIOR AUTHORIZATION CLINICAL CRITERIA FOR APPROVAL
Module |
Clinical Criteria for Approval |
PA |
Initial Evaluation Target Agent(s) will be approved when ALL of the following are met:
Length of Approval: 3 months NOTE: If Quantity Limit applies, please refer to Quantity Limit Criteria.
Renewal Evaluation Target Agent(s) will be approved when ALL of the following are met:
Length of Approval: 12 months NOTE: If Quantity Limit applies, please refer to Quantity Limit Criteria. |
QUANTITY LIMIT CLINICAL CRITERIA FOR APPROVAL
Module |
Clinical Criteria for Approval |
QL with PA |
Quantity Limit for the Target Agent(s) will be approved when ONE of the following is met:
Length of Approval: up to 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.
Commercial _ PS _ Sucraid_sacrosidase__PAQL _ProgSum_ 01-01-2025