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Study to Assess Linsitinib in Participants With Moderate to Severe Active Thyroid Eye Disease (TED)

RecruitingPhase 3

A Phase 3, Randomized, Double-mask, Placebo-controlled Study With Open-label Extension to Evaluate the Efficacy and Safety of Linsitinib in Participants With Moderate to Severe Active Thyroid Eye Disease (TED)

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. Participants must be ≥ 18 years of age at Screening
2. Clinical diagnosis of Graves' Disease and/or autoimmune Hashimoto's thyroiditis associated with active moderate to severe TED with a CAS ≥ 3 (on the 7-item scale) for the most severely affected eye (primary study eye) at Screening and Baseline.
3. Moderate to severe active TED (not sight-threatening but has an appreciable impact on daily life), with diagnosis of TED within 15 months prior to the Screening visit and usually associated with 1 or more of the following: lid retraction ≥ 2 mm, moderate or severe soft tissue involvement, proptosis ≥ 3 mm above normal for race and gender, and/or inconstant or constant diplopia.
4. Participants must be euthyroid with the participant's baseline disease under control or have mild hypo- or hyperthyroidism (defined as free thyroxine \[FT4\] and free triiodothyronine levels \[FT3\] \< 50% above or below the normal limits of the central laboratory) at Screening.
5. Does not require immediate ophthalmic surgery, radiotherapy to orbits or other ophthalmological intervention at the time of Screening and is not planning for any such treatment during the course of the study.

Exclusion Criteria:

1. Any progressing optic neuropathy due to TED that has worsened in the last 6 months in the opinion of the investigator.
2. Corneal decompensation unresponsive to medical management.
3. Previous orbital irradiation or orbital surgery in either eye.
4. Any glucocorticoid use (IV or oral) with a cumulative dose equivalent to ≥ 1 g of methylprednisolone or equivalent for the treatment of TED within 8 weeks of Screening.
5. Prior IGF-1R inhibitor therapy for any condition.

About the study

The goal of this clinical trial is to evaluate the efficacy, safety, and tolerability of linsitinib in participants with moderate to severe Thyroid Eye Disease (TED).

What is being tested

Sponsor: Sling Therapeutics, Inc. · Participants: 130 · Started: Aug 4, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07753603

Locations in the U.S.

ArizonaSun City Clinical Research, Glendale
CaliforniaThrive Health Research LLC, Beverly Hills
Alliance Research Institute, Canoga Park
Pasadena Clinical Trials, Pasadena
Silkiss Eye Surgery, San Francisco
Advancing Research International, LLC, Santa Monica
FloridaFlorida International Medical Research, Coral Gables
Rovia Clinical Research at Florida Eye Specialists, Jacksonville
MassachusettsOphthalmic Consultants of Boston, Inc, East Weymouth
MichiganKahana Oculoplastic & Orbital Surgery, Livonia
NevadaAdvancing Research International, Las Vegas
Vector Clinical Trials, Reno
New JerseyThe Center for Eye and Facial Plastic Surgery, Somerset
New YorkColumbia University Ophthalmology, New York (Not yet recruiting)
North CarolinaAsheville Clinical Trials, Asheville
TexasGulf Coast Clinical Trials, Houston
VirginiaVirginia Eye Consultants, Norfolk
West VirginiaWVU Eye Institute, Morgantown

Conditions

From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.