Please ensure JavaScript is enabled for purposes of website accessibility TEPEZZA® (teprotumumab-trbw) Patient Results | For HCPs

Patient Results With TEPEZZA

TEPEZZA can help patients regardless of disease activity or duration1-4

  • Before
  • After

79-year-old male patient, living with TED for 2 years

PRE-TREATMENT

PRE-TREATMENT

Visible signs:

Proptosis (28 mm OD; 25 mm OS), eyelid swelling, conjunctival redness

Nonvisible symptoms:

Intermittent diplopia

Impact on daily living:

Difficulty reading, lowered self-esteem

See the Burden-Impact Model for this patient

79-year-old male patient, living with TED for 2 years

After-treatment

Improvements after 8 infusions

Visible signs:

Proptosis (24 mm OD; 22 mm OS)

Nonvisible symptoms:

Diplopia resolved

Daily living:

“I’ve been treating patients with TEPEZZA since 2020 and it has had a huge impact.” – Amina Malik, MD

See the Burden-Impact Model for this patient

  • Before
  • After

55-year-old male patient, living with TED for 20 years

Before-treatment-55-year-old 

PRE-TREATMENT

Visible signs:

Proptosis (22 mm OD; 23 mm OS), eyelid swelling, conjunctival redness

Nonvisible symptoms:

Constant diplopia, eye pain, and burning sensation

Impact on daily living:

Lowered work productivity due to diplopia; reduced self-esteem

Orbital MRI

See the Burden-Impact Model for this patient

55-year-old male patient, living with TED for 20 years

After-treatment-55-year-old 

Improvements after 8 infusions

Visible signs:

Proptosis (20 mm OD; 21 mm OS)

Nonvisible symptoms:

Intermittent diplopia, eye pain and burning sensation resolved

Daily living:

Patient reported improvement in daily activities; happy with results

Orbital MRI

See the Burden-Impact Model for this patient

IMPORTANT SAFETY INFORMATION

WARNINGS AND PRECAUTIONS

Infusion Reactions: TEPEZZA may cause infusion reactions. Infusion reactions have been reported in approximately 4% of patients treated with TEPEZZA. Reported infusion reactions have usually been mild or moderate in severity. Signs and symptoms may include transient increases in blood pressure, feeling hot, tachycardia, dyspnea, headache, and muscular pain. Infusion reactions may occur during an infusion or within 1.5 hours after an infusion. In patients who experience an infusion reaction, consideration should be given to premedicating with an antihistamine, antipyretic, or corticosteroid and/or administering all subsequent infusions at a slower infusion rate.

Inflammatory Bowel Disease: TEPEZZA may cause an exacerbation of inflammatory bowel disease (IBD). IBD has been reported in some patients without a prior diagnosis of IBD. Monitor patients for signs and symptoms of IBD. If IBD exacerbation is suspected, discontinue use of TEPEZZA.

Hyperglycemia: Increased blood glucose or hyperglycemia may occur in patients treated with TEPEZZA. In clinical trials, 10% of patients (two-thirds of whom had preexisting diabetes or impaired glucose tolerance) experienced hyperglycemia. Hyperglycemic events should be controlled with medications for glycemic control, if necessary. Assess patients for elevated blood glucose and symptoms of hyperglycemia prior to infusion and continue to monitor while on treatment with TEPEZZA. Ensure patients with hyperglycemia or preexisting diabetes are under appropriate glycemic control before and while receiving TEPEZZA.

Hearing Impairment Including Hearing Loss: TEPEZZA may cause severe hearing impairment including hearing loss, which in some cases may be permanent. Assess patients’ hearing before, during, and after treatment with TEPEZZA and consider the benefit-risk of treatment with patients.

ADVERSE REACTIONS

The most common adverse reactions (incidence ≥5% and greater than placebo) are muscle spasm, nausea, alopecia, diarrhea, fatigue, hyperglycemia, hearing impairment, dysgeusia, headache, dry skin, ear discomfort, weight decreased, nail disorders, and menstrual disorders.

INDICATION

TEPEZZA is indicated for the treatment of Thyroid Eye Disease regardless of Thyroid Eye Disease activity or duration.

Please see Full Prescribing Information for more information.

  • REFERENCES:
    1. TEPEZZA (teprotumumab-trbw) [prescribing information] Amgen. 2. Smith TJ, Kahaly GJ, Ezra DG, et al. Teprotumumab for thyroid-associated ophthalmopathy. N Engl J Med. 2017;376(18):1748-1761. 3. Douglas RS, Couch S, Wester ST, et al. Efficacy and safety of teprotumumab in patients with thyroid eye disease of long duration and low disease activity. J Clin Endocrinol Metab. 2024;109(1):25-35. 4. Douglas RS, Kahaly GJ, Patel A, et al. Teprotumumab for the treatment of active thyroid eye disease. N Engl J Med. 2020;382(4):341-352. 5. Barrio-Barrio J, Sabater AL, Bonet-Farriol E, et al. Graves' ophthalmopathy: VISA versus EUGOGO classification, assessment, and management. J Ophthalmol. 2015:2015:249125. 6. Bothun ED, Scheurer RA, Harrison AR, et al. Update on thyroid eye disease and management. Clin Ophthalmol. 2009;3:543-551. 7. Cockerham KP, Padnick-Silver L, Stuertz N, et al. Quality of life in patients with chronic Thyroid Eye Disease in the United States. Ophthalmol Ther. 2021;10:975-987. 8. Park JJ, Sullivan TJ, Mortimer RH, et al. Assessing quality of life in Australian patients with Graves’ ophthalmopathy. Br J Ophthalmol. 2004 Jan;88(1):75-78. 9. Kahaly GJ, Petrak F, Hardt J, et al. Psychosocial morbidity of Graves' orbitopathy. Clin Endocrinol (Oxf). 2005:63(4):395-402. 10. Estcourt S, Vaidya B, Quinn A, et al. The impact of thyroid eye disease upon patients' wellbeing: a qualitative analysis. Clin Endocrinol (Oxf). 2008:68(4):635-639.

IMPORTANT SAFETY INFORMATION

WARNINGS AND PRECAUTIONS Infusion Reactions: TEPEZZA may cause infusion reactions. Infusion reactions have been reported in approximately 4% of patients treated with TEPEZZA. Reported infusion reactions have usually been mild or moderate in severity. Signs and symptoms may include transient increases in blood pressure, feeling hot, tachycardia, dyspnea, headache, and muscular pain. Infusion reactions