Subject: Specialty Quantity Limit Ninlaro 2995-H P2022
Policy:
I. PROGRAM DESCRIPTION
The standard limit is designed to allow a quantity sufficient for
the most common uses of the medication. The recommended
dosing parameters for all FDA-approved indications fall within
the standard limits. Coverage of an additional quantity may be
reviewed on a case-by-case basis upon request.
II. COVERED QUANTITIES
|
Medication
|
Standard Limit
|
FDA-recommended dosing
|
|
Ninlaro (ixazomib)
4 mg capsules
|
3 per 28 days
|
Recommended starting dose
of 4 mg taken orally on days 1,
8, and 15 of a 28-day cycle
Dose reductions due to adverse
reactions:
• First reduction to 3 mg
• Second reduction to 2.3 mg
|
|
Ninlaro (ixazomib)
3 mg capsules
|
3 per 28 days
|
|
Ninlaro (ixazomib)
2.3 mg capsules
|
3 per 28 days
|
Place of Service:
Outpatient
The above policy is based on the following references:
1. Ninlaro [package insert]. Lexington, MA: Takeda Pharmaceuticals
America, Inc.; May
Copyright Aetna Inc. All rights reserved. Pharmacy Clinical Policy Bulletins are developed by Aetna to assist in administering plan benefits and constitute neither offers of coverage nor medical advice. This Clinical Policy Bulletin contains only a partial, general description of plan or program benefits and does not constitute a contract. Aetna does not provide health care services and, therefore, cannot guarantee any results or outcomes. Participating providers are independent contractors in private practice and are neither employees nor agents of Aetna or its affiliates. Treating providers are solely responsible for medical advice and treatment of members. This Clinical Policy Bulletin may be updated and therefore is subject to change.
April 15, 2023
