Effective Date:
a) This policy will apply to all services performed on or after the above revision date which will become the new effective date.
b) For all services referred to in this policy that were performed before the revision date, contact customer service for the rules that would apply.
1) Talvey (talquetamab-tgvs) requires prior authorization.
2) Talvey is used to patients with relapsed or refractory multiple myeloma.
3) Talvey is covered under the medical benefit.
Initial Approval Criteria
I. Multiple Myeloma (must meet all):
a. Diagnosis of MM;
b. Prescribed by or in consultation with an oncologist or hematologist;
c. Age > 18 years;
d. Disease is relapsed or refractory;
e. Member has received or has documented intolerance to > 4 lines of therapies that include all of the following:
i. One proteasome inhibitor (e.g. bortezomib, Kyprolis, Ninlaro);
ii. One immunomodulatory drug (e.g. Thalomid, lenalidomide, pomalidomide);
iii. One anti-CD38 monoclonal antibodies (e.g. Darzalex, Sarclisa)
f. Dosing is consistent with FDA-labeling
Approval Duration: 6 months
1. Talvey Prescribing Information. Horsham, PA: Janssen Biotech, Inc.; Aug 2023. Available at: www.talvey.com. Accessed August 23, 2023.
2. National Comprehensive Cancer Network. Multiple Myeloma Version 3.2023. Available at: https://www.nccn.org/professionals/physician_gls/pdf/myeloma.pdf. Accessed August 23, 2023.
3. Chari A, Minnema MC, Berdeja JG, et al. Talquetamab, a t-cell–redirecting gprc5d bispecific antibody for multiple myeloma. New England Journal of Medicine. 2022;387(24):2232-2244.