This is a promotional material developed and funded by Amgen for UK Healthcare Professionals and Other Relevant Decision Makers only.
Prescribing information and adverse event reporting information can be found at the end of this experience or by pressing here.
GBR-632-26-80009 | Feb 26
This webAR experience is provided for educational and awareness purposes only.
It uses on-device face tracking and visual effects to simulate the appearance of certain signs that may be associated with Thyroid Eye Disease (TED).
This experience is not a medical device, not a diagnostic tool, and not intended to predict, prevent, monitor, treat, or cure any disease.
The visual effects are illustrative only and may not reflect how TED appears for any individual, including severity, progression, or combinations of symptoms.
This experience does not provide medical advice. If you have symptoms or concerns, please consult a qualified healthcare professional.
This tool is not intended to represent how TED manifests in all patients and users should be aware that the signs, symptoms and how each patient experiences TED may vary. All image representations have been created and tested with healthcare professionals experienced in the diagnosis and management of TED and deemed to be suitable to depict some of the changes that can be seen with the disease.
Do not use if you are sensitive to visual effects, experience dizziness, nausea, or discomfort. Stop immediately if you feel unwell.
Use in a safe environment and remain aware of your surroundings.
Face tracking is processed on your device to apply effects. This experience does not store or retain face images.
No responses to questions within this experience will be captured, stored, or retained. No images will be stored or collected during this experience.
By selecting “I Agree”, you confirm that you have read and understood the information above and wish to proceed.
This is a promotional material developed and funded by Amgen for UK Healthcare Professionals and Other Relevant Decision Makers only.
Prescribing information and adverse event reporting information can be found at the end of this experience or by pressing here.
Please click to watch this 1 minute video of a patient discussing her experience with TED before continuing. Allow access to device camera when asked.
This is a promotional material developed and funded by Amgen for UK Healthcare Professionals and Other Relevant Decision Makers only.
Prescribing information and adverse event reporting information can be found at the end of this experience or by pressing here.
TEPEZZA®▼ (teprotumumab) is the first UK targeted treatment indicated in adults for the treatment of Moderate-To-Severe Thyroid Eye Disease (TED)1
Efficacy of teprotumumab in adults with active
moderate-to-severe TED at week 24:


vs 10% (n=4/42) with placebo2.3 Intention To Treat analysis. Treatment difference 73.45% [58.89 to 88.01]; P<0.001


vs 29% (n=8/28) with placebo3 Intention To Treat analysis. Treatment difference 39% [95% CI: 16 to 63]; P=0.001


vs 4.43±2.10 with placebo (n=42)3 Treatment difference 9.36 [95% CI: 4.08 to 14.64]; P<0.001
* A proptosis responder was defined as having a ≥2-mm reduction in proptosis from baseline in the study eye without deterioration (≥2-mm increase in proptosis) in the non-study eye at week 24.
** A diplopia response was defined as a reduction in Gorman diplopia score of ≥1 grade from baseline.
*** A mixed-model repeated-measures analysis of covariance was used to assess the secondary outcome change from baseline in overall score on the Graves’ ophthalmopathy-specific quality-of-life (GO-QOL) questionnaire.
1) https://www.amgen.co.uk/media/news-release/2025/05/amgens-tepezza-teprotumumab-granted-marketing-authorisation-as-the-first-targeted-treatment-specifically-for-adults-with-moderate-to-severe-thyroid-eye-disease-ted-in-the-United-Kingdom. Accessed Jan 2026
2) TEPEZZA®▼ (teprotumumab) SmPC. 3) Douglas RS, Kahaly GJ, Patel A et al N Eng J Med 2020; 382(4):341-352.
Scan this QR code to view
Prescribing Information
This is a promotional material developed and funded by Amgen for UK Healthcare Professionals and Other Relevant Decision Makers only.
Prescribing information and adverse event reporting information can be found on this page.
Thank you for completing the TED simulation journey. Please speak to your Amgen Account Manager for further information.
This is a promotional material developed and funded by Amgen for UK Healthcare Professionals and Other Relevant Decision Makers only.
Prescribing information and adverse event reporting information can be found on the previous page of this experience or by pressing here.
GBR-632-26-80009 | Feb 2026 © 2026 Amgen Limited. All rights reserved
This tool is not intended to represent how TED manifests in all patients and users should be aware that the signs, symptoms and how each patient experiences TED may vary.
This is a promotional material developed and funded by Amgen for UK Healthcare Professionals and Other Relevant Decision Makers only.
Prescribing information and adverse event reporting information can be found at the end of this experience or by pressing here.
This tool is not intended to represent how TED manifests in all patients and users should be aware that the signs, symptoms and how each patient experiences TED may vary.


This is a promotional material developed and funded by Amgen for UK Healthcare Professionals and Other Relevant Decision Makers only.
Prescribing information and adverse event reporting information can be found at the end of this experience or by pressing here.
This tool is not intended to represent how TED manifests in all patients and users should be aware that the signs, symptoms and how each patient experiences TED may vary.


This is a promotional material developed and funded by Amgen for UK Healthcare Professionals and Other Relevant Decision Makers only.
Prescribing information and adverse event reporting information can be found at the end of this experience or by pressing here.
(1 - no impact → 5 - severe impact)