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Specialty Pharmacy Clinical Policy Bulletins
Aetna Non-Medicare Prescription Drug Plan
Subject: Nubeqa 3147-A SGM P2023

Drug
NUBEQA  (darolutamide)


Policy:

      I.  INDICATIONS

          The indications below including FDA-approved indications and
          compendial uses are considered a covered benefit provided that
          all the approval criteria are met and the member has no
          exclusions to the prescribed therapy.

          A.  FDA-Approved Indications
               1.  Nubeqa is indicated for the treatment of adult patients
                    with non-metastatic castration-resistant prostate cancer
                    (nmCRPC).
               2.  Nubeqa is indicated for the treatment of adult patients
                    with metastatic hormone-sensitive prostate cancer
                    (mHSPC) in combination with docetaxel.

          B.  Compendial Use
               Prostate Cancer

          All other indications are considered experimental/investigational
          and not medically necessary.


    II.  EXCLUSIONS

          Coverage will not be provided if the requested medication is
          used in combination with a second-generation oral anti-
          androgen (e.g., apalutamide [Erleada]) or an oral androgen
          metabolism inhibitor (e.g., abiraterone acetate [Zytiga]).


  III.  CRITERIA FOR INITIAL APPROVAL

          Prostate Cancer
          Authorization of 12 months may be granted when either of the
          following criteria are met:
          1.  The member has non-metastatic castration-resistant prostate
               cancer and the member has had a bilateral orchiectomy or
               will be using the requested medication in combination with a
               GnRH agonist or degarelix.
          2.  The member has metastatic hormone-sensitive prostate
               cancer and meets both of the following criteria:
               i.     The requested drug will be used in combination with
                      docetaxel
               ii.    The member has had a bilateral orchiectomy or will be
                      using the requested medication in combination with a
                      GnRH agonist or degarelix.


   IV.  CONTINUATION OF THERAPY

          Authorization of 12 months may be granted for continued
          treatment in members requesting reauthorization for an
          indication listed in Section III when there is no evidence of
          unacceptable toxicity or disease progression while on the current
          regimen.


Place of Service:

Outpatient

The above policy is based on the following references:
  1. Nubeqa [package insert]. Whippany, NJ: Bayer Healthcare Pharmaceuticals Inc.; August 2022.
  2. The NCCN Drugs & Biologics Compendium™ © 2023 National Comprehensive Cancer Network, Inc. https://www.nccn.org Accessed August 6, 2023.
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.

December 09, 2023
Aetna
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