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Clinical Trial Summary

The primary objective of this clinical trial is to assess the safety and tolerability of sub-tenon aflibercept in combination with either saline or hyaluronidase (HA) in patients with acute Thyroid Eye Disease (TED) as assessed by the incidence and severity of adverse events from baseline to day 45. Participants will undergo clinical examinations and receive three injections of aflibercept with saline, aflibercept with hyaluronidase, or hyaluronidase.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04311606
Study type Interventional
Source Massachusetts Eye and Ear Infirmary
Contact Nahoung Grace Lee, MD
Phone 617-572-5550
Email Grace_Lee@MEEI.HARVARD.EDU
Status Recruiting
Phase Phase 2
Start date November 2, 2020
Completion date January 1, 2027

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