Topic

Zokinvy (lonafarnib)

A collection of 30 issues

How to Get Zokinvy (lonafarnib) Covered by Cigna in Virginia: Complete PA Guide with Appeal Templates

Answer Box: Getting Zokinvy (lonafarnib) Approved by Cigna in Virginia Cigna covers Zokinvy (lonafarnib) for HGPS and processing-deficient progeroid laminopathies through Express Scripts with prior authorization. Coverage requires patient age ≥12 months, BSA ≥0.39 m², genetic confirmation of pathogenic LMNA variant, and prescription by a geneticist or pediatric cardiologist.
6 min read

Coding That Helps Get Zokinvy (Lonafarnib) Approved in Illinois with Aetna (CVS Health): ICD-10, HCPCS/J-Code, NDC

Answer Box Zokinvy (lonafarnib) requires prior authorization from Aetna (CVS Health) using ICD-10 code E34.8 (progeria), HCPCS J8499, and specific NDCs (60923-0544-53, 73079-0050-30). Submit genetic confirmation, BSA calculations, and specialist oversight through CVS Specialty Pharmacy. Illinois residents have 4 months to file external appeals through the Illinois Department of
5 min read

How to Get Zokinvy (lonafarnib) Covered by UnitedHealthcare in Virginia: Complete PA Guide with Appeal Scripts

Answer Box: Getting Zokinvy Covered by UnitedHealthcare in Virginia Zokinvy (lonafarnib) requires prior authorization from UnitedHealthcare and is typically non-formulary, requiring a coverage exception. The fastest path: 1) Submit PA through the UHC Provider Portal with genetic confirmation of HGPS/progeroid laminopathy, 2) Include medical necessity letter citing FDA approval
7 min read

How to Get Zokinvy (lonafarnib) Covered by UnitedHealthcare in New York: Complete Appeal Guide

Quick Answer: Getting Zokinvy Covered by UnitedHealthcare in New York UnitedHealthcare requires prior authorization for Zokinvy (lonafarnib) with specific genetic testing requirements. For HGPS patients, you need confirmed diagnosis only. For progeroid laminopathies, you must document heterozygous LMNA mutation with progerin-like protein accumulation OR homozygous/compound heterozygous ZMPSTE24 mutations. Submit
6 min read