Horizon Therapeutics announced new Tepezza (teprotumumab-trbw) data will be presented at the American Academy of Ophthalmology Annual Meeting, Nov. 13-15, 2020. Tepezza is the first and only medicine approved by the FDA for the treatment of Thyroid Eye Disease (TED) – a serious, progressive and vision-threatening rare autoimmune disease.1
Tepezza data being presented at AAO 2020 Virtual include:
- Long-Term Assessment of Proptosis and Diplopia from the OPTIC Trial of Teprotumumab in Thyroid Eye Disease
- Session: PA038, R. Douglas
- Date: On Demand (oral presentation)
- Improvement in the Fellow Eye of Patients With TED: Pooled Analyses from the Teprotumumab Studies
- Session: PO305, R. Douglas
- Date: On Demand (scientific poster)
- Dysthyroid Optic Neuropathy Response to Teprotumumab: Early Response to Therapy
- Session: PO307, C. Sears
- Date: On Demand (scientific poster)
Independent study
- What Every Ophthalmologist Should Know About Teprotumumab
- Session: OCU03V, R. Douglas
- Date: Friday, Nov. 13, 2020; 1:07 p.m. PT (live broadcast)
- Plastics: Biologics for Orbital Disease (teprotumumab)
- Session: SYM17V, R. Douglas
- Date: Sunday, Nov. 15, 2020; 2:05 p.m. PT (live broadcast)
In addition, Horizon will host a virtual product theater on Friday, Nov. 13 at 4:30 p.m. PT about Tepezza, featuring Raymond Douglas, MD, PhD, director of the Orbital and Thyroid Eye Disease Program, Cedars-Sinai Medical Center.
- Barrio-Barrio J, et al. Graves’ Ophthalmopathy: VISA versus EUGOGO Classification, Assessment, and Management. Journal of Ophthalmopathy. 2015;2015:1-16.