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Evaluation of ETHY-001 for Safety, Tolerability, and Clinical Activity in Thyroid Eye Disease

NCT07885605

This study is recruiting at 2 US sites in 2 states, according to its ClinicalTrials.gov record last updated .

Summary

The primary objective of study is to investigate the safety, tolerability, pharmacokinetics, and pharmacodynamics of ETHY-001 in healthy volunteers and participants with Thyroid Eye Disease after single subcutaneous doses.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Thyroid Eye Disease (TED)
  • Graves' Disease
  • Eye Diseases, Hereditary
  • Eye Diseases
  • Exophthalmos
  • Orbital Diseases
  • Goiter
  • Thyroid Diseases
  • Endocrine System Diseases
  • Hyperthyroidism
  • Autoimmune Diseases
  • Immune System Diseases
  • Graves Ophthalmopathy
  • Proptosis

Eligibility basics and study details

Study type
Interventional
Phase
Phase 1
Ages
18 years and older
Sex
All
Healthy volunteers
Accepted
Sponsor
Ethyreal Bio, Inc.
Last updated on ClinicalTrials.gov
October 26, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

Illinois · 1

  • Site 105 · Orland Park, IL

North Carolina · 1

  • Site 113 · Wilmington, NC

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.