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Thyroid eye disease

Part of Graves' disease

2 published articles · Updated continuously

Clinical Trial Landscape

Clinical Trials for thyroid eye disease

5 trials tracked for thyroid eye disease: 3 in phase 3 or 4 and 2 with published results. The most-cited published study has 702 citations.

5Trials tracked
3Phase 3 & 4
0Recruiting
2With published results
Phase distribution
Phase 4 1 Phase 3 2 Phase 2 1 Other / NA 1
  1. Phase 3 Treatment of Graves' Orbitopathy (Thyroid Eye Disease) to Reduce Proptosis With Teprotumumab Infusions in a Randomized, Placebo-Controlled, Clinical Study Completed · 702 cited
  2. Phase 3 Treatment of Graves' Orbitopathy to Reduce Proptosis With Teprotumumab Infusions in an Open-Label Clinical Extension Study Completed · 28 cited
  3. Phase 4 A Study Evaluating TEPEZZA® Treatment in Patients With Chronic (Inactive) Thyroid Eye Disease Completed
  4. Phase 2 A Study to Evaluate the Efficacy and Safety of LASN01 in Patients With Thyroid Eye Disease Completed
  5. N/A Twenty-four Hour Intraocular Pressure Patterns in Patients With Uncontrolled Thyroid Eye Disease Completed

Showing the 5 most-cited and recently-updated of 5 trials. Browse the full registry →

Trial data sourced from ClinicalTrials.gov. Counts describe the research landscape and are not a treatment recommendation. Informational only — not medical advice.

What the trials found Updated — new results For clinicians

Thyroid eye disease: what the trials found

Teprotumumab (also referred to as TEPEZZA) has demonstrated significant efficacy in treating thyroid eye disease. Clinical trials showed a statistically significant reduction in proptosis at week 24, with mean changes of -2.41 mm and -0.92 mm respectively (p=0.0004) 2.

In Phase 3 studies using Teprotumumab, high responder rates were observed for both proptosis reduction (82.9% vs 9.5%, p<0.001) and overall clinical response (78.0% vs 7.1%, p<0.001) 3. Furthermore, approximately 89.2% of patients achieved a ≥ 2 mm reduction in proptosis in the study eye without deterioration in the fellow eye at week 24 4.

Teprotumumab also showed significant improvements in clinical activity scores (CAS). Specifically, 58.5% of patients were categorized as CAS responders compared to 21.4% in the control group (p<0.001) 3, and 65.6% achieved an EUGOGO amended CAS score of 0 or 1 at week 24 4. Additionally, 75.0% of patients were identified as diplopia responders 4.

Recent results — preliminary, needs further review

  • LASN01 was evaluated in a Phase 2 trial; however, results showed only 6 participants achieved a response in proptosis (≥ 2 mm decrease) and 15 participants showed a response in Clinical Activity Score (CAS) 1.

For the clinician treating this condition

  • Teprotumumab is associated with significant reductions in proptosis and improved clinical activity scores (CAS) in patients with thyroid eye disease.
  • High percentages of patients treated with Teprotumumab achieved a ≥ 2 mm reduction in proptosis without worsening in the fellow eye, while also showing high rates of diplopia response.

AI synthesis of 4 cited trials, updated Jun 29, 2026. Informational only — not medical advice; trial data sourced from ClinicalTrials.gov. How we use AI.

HCP Mode — summaries include clinical detail, trial data, and statistical outcomes.
Patient Mode — summaries use plain language, avoiding clinical jargon.

Research across Graves' disease

Related studies from across the Graves' disease family.