Proven efficacy with a demonstrated safety and tolerability profile, regardless of disease activity or duration
9 out of 10
completed full course of
treatment with TEPEZZA1
Most adverse events were:1
-
Mild or moderate
-
Manageable
-
Resolved during or after treatment
Adverse reactions occurring in ≥5% of patients treated with TEPEZZA with greater incidence than placebo2
|
Adverse reactions |
TEPEZZA n=84, n (%) |
Placebo n=86, n (%) |
|---|---|---|
|
Muscle spasms |
21 (25%) |
6 (7%) |
|
Nausea |
14 (17%) |
8 (9%) |
|
Alopecia |
11 (13%) |
7 (8%) |
|
Diarrhea |
10 (12%) |
7 (8%) |
|
Fatiguea |
10 (12%) |
6 (7%) |
|
8 (10%) |
1 (1%) |
|
|
8 (10%) |
0 |
|
|
Dysgeusia (taste disturbance) |
7 (8%) |
0 |
|
Headache |
7 (8%) |
6 (7%) |
|
Dry skin |
7 (8%) |
0 |
|
Weight decreased |
5 (6%) |
0 |
|
Nail disorderd |
4 (5%) |
0 |
|
Menstrual disorderse |
5 (23%) |
1 (4%) |
Hyperglycemia: previous glycemic abnormalities in patients receiving TEPEZZA1
In the Phase 2 and 3 studies (N=84)1
10% (n=8/84)
of patients experienced a hyperglycemic event1
63% (n=5/8)
of patients who experienced a hyperglycemic event had preexisting diabetes1
The majority of hyperglycemia events resolved during or shortly after treatment1
-
Of 8 total events, 6 resolved during treatment, 2 resolved after the last dose
Most hearing impairment events were transient, mild or moderate, and resolved during or after treatment1
In the Phase 2 and 3 studies (N=84)1
10% (n=8/84)
of patients experienced a hearing
impairment event1
75% (n=6/8)
of the cases of hearing impairment resolved,
and 1 case improved, during the 24-week
double-masked period1
In an observational study, patients at greatest risk of hearing impairment events caused by TEPEZZA:3,*
-
Are older age (>65) with a higher CAS
-
Have preexisting hearing issues
>9 out of 10
completed treatment with TEPEZZA 4
Adverse events of special interest and other AEs of importance4
|
Adverse reactions |
TEPEZZA n=41,n (%) |
Placebo n=20,* n (%) |
|---|---|---|
|
Muscle spasms |
17 (42%) |
2 (10%) |
|
Fatigue |
9 (22%) |
2 (10%) |
|
9 (22%) |
2 (10%) |
|
|
Diarrhea |
8 (20%) |
4 (20%) |
|
Headache |
7 (17%) |
2 (10%) |
|
6 (15%) |
2 (10%) |
|
|
Dry skin |
5 (12%) |
0 |
|
Dysgeusia |
4 (10%) |
1 (5%) |
|
Infusion reaction |
7 (8%) |
3 (15%) |
|
Nausea |
2 (5%) |
1 (5%) |
|
Alopecia |
2 (5%) |
0 (0%) |
|
Nail bed disorder |
2 (5%) |
0 (0%) |
Most adverse events were:4
-
Mild or moderate
-
Manageable
-
Resolved during or after treatment (as assessed in 30-day follow-up period)
Hyperglycemia: previous glycemic abnormalities in patients receiving TEPEZZA4
In the Phase 4 study (N=41):4
15% (n=6/41)
of patients experienced a
hyperglycemic event4
83% (n=5/6)
of patients who experienced a
hyperglycemic event had preexisting
diabetes or possibility of preexisting
diabetes/impaired glucose tolerance4,*
The majority of hyperglycemic events were managed with adjustment of medication with none leading to discontinuation of treatment4
Hearing impairments were mostly mild or moderate4
In the Phase 4 study (N=41):4
22% (n=9/41)
of patients who received TEPEZZA
experienced a hearing impairment event4
33% (n=3/9)
of cases of hearing impairment
resolved/resolving at 30-day follow-up4
Patients at greatest risk of hearing impairment events caused by TEPEZZA:3,*
-
Are older age (>65) with a higher CAS
-
Have preexisting hearing issues
CAS, Clinical Activity Score.
For any additional questions regarding the safety profile or adverse events, please speak with your Amgen Representative.
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