Recruiting
Phase 3

Linsitinib

Sponsor:

Sling Therapeutics, Inc.

Code:

NCT07753603

Conditions

Thyroid Eye Disease, TED

Graves Orbitopathy

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

linsitinib

Placebo

Study Details

Brief summary:

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).

Conditions

Thyroid Eye Disease, TED

Graves Orbitopathy

Study ID

NCT07753603

Start date

Aug 4, 2026

Status verified date

Aug, 2026

Completion date

Jun 28, 2030

Anticipated

Primary completion date

Jun 30, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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.

Study Design

Enrollment

130 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Double-mask Treatment Arm

Participants receive linsitinib 150 mg twice daily for 24 weeks.

placebo comparator: Double-mask Placebo Arm

Participants receive placebo 0 mg twice daily for 24 weeks.

experimental: Open-label Extension Treatment Arm

Proptosis non-responders/relapsed proptosis responders receive linsitinib 150 mg twice daily for 24 weeks.

Interventions

linsitinib

150 mg linsitinib is taken twice daily by mouth for 24 weeks

Placebo

0 mg placebo taken twice daily by mouth for 24 weeks

Primary outcome measure

  • Measure percentage of participants who are Proptosis Responders at Week 24 [ Time Frame: 24 weeks ]

Central Contacts and Locations

Central contacts

Locations

Advancing Research International

Recruiting

Las Vegas, Nevada, United States, 89144

More Information

Sponsor

Sling Therapeutics, Inc.

Last update posted

Aug 11, 2026

Last verified

Aug, 2026

Keywords

  • Thyroid Eye Disease
  • TED
  • Graves Orbitopathy
  • Graves' Disease
  • Hashimoto's thyroiditis

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Sling Therapeutics, Inc. on 2026-08-11.