I.
Initial Approval Criteria A. Thyroid Eye Disease
(must meet all):
A. Diagnosis of Graves’
disease with associated TED (i.e., Graves’ ophthalmopathy, Graves’ orbitopathy);
B. Member has active TED
with a clinical activity score (CAS) of ≥ 4 (see Appendix D);
C. Prescribed by or in
consultation with an ophthalmologist;
D. Age ≥ 18 years;
E. One of the following
(a or b):
a. Member is euthyroid
with documentation of a recent (within the last 30 days) free thyroxine (FT4)
and total triiodothyronine (T3) or free T3 (FT3) levels within the laboratory
defined reference range;
b. Member has a recent
(within the last 30 days) free thyroxine (FT4) and total triiodothyronine (T3)
or free T3 (FT3) levels less than 50% above or below the laboratory defined
reference range and is undergoing treatment to correct the mild hypo- or
hyperthyroidism to maintain a euthyroid state;
F. Member has not had
previous surgical intervention for TED;
G. Member does not
require surgical ophthalmological intervention;
H. Failure of a 4-week
trial of a systemic corticosteroid (at up to maximally indicated doses), unless
clinically significant adverse effects are experienced or all are
contraindicated;
I. Member has not
received ≥ 8 Tepezza infusions (including the initial 10 mg/kg first infusion);
J. Dose does not exceed
both of the following (a and b):
a. A single 10 mg/kg dose
followed by seven 20 mg/kg infusions given every 3 weeks;
b. Vial quantity as
identified by the online dose calculator using the member’s weight or as
recommended in for vial rounding.
Approval duration: 6 months (up to 8 total lifetime infusions)
II.
Continued Therapy
A. Thyroid Eye Disease
(must meet
all):
1. Member is currently
receiving medication via QualChoice benefit or member has previously met initial
approval criteria;
2. Member is responding
positively to therapy as evidenced by both of the following (a and b):
a. Reduction in proptosis
≥ 2 mm;
b. Reduction in CAS from
baseline of ≥ 2 points;
3. Member has not had
previous surgical intervention for TED;
4. Member does not
require surgical ophthalmological intervention;
5. Member has not
received ≥ 8 Tepezza infusions (including the initial 10 mg/kg first infusion);
6. If request is for a
dose increase, new dose does not exceed both of the following (a and b):
a. A total of seven 20
mg/kg infusions given every 3 weeks;
b. Vial quantity as
identified by the online dose calculator using the member’s weight or as
recommended for vial rounding.
Approval duration: 6 months (up to 8 total lifetime infusions)
Codes
Used In This BI:
1)
J3241 – Injection,
teprotumumab-trbw, 10mg