Lonigutamab for Thyroid Eye Disease
(TED Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new treatment called lonigutamab for individuals with Thyroid Eye Disease (TED). Researchers aim to determine if different doses of lonigutamab can reduce symptoms such as bulging eyes. Participants will receive injections of either lonigutamab or a placebo (a substance with no active treatment). Ideal candidates are those who have recently developed TED symptoms and have noticeable eye bulging (3 mm above normal). This study excludes individuals with certain eye conditions or those who have previously used specific treatments. As a Phase 1 trial, this research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new treatment.
Do I need to stop my current medications for the trial?
The trial requires that you have not used certain medications recently, like steroids for TED, IGF-1R inhibitors, or other immunosuppressive agents. If you're on these, you might need to stop them before joining, but the protocol doesn't specify about other medications.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Research shows that lonigutamab is being tested for safety in treating thyroid eye disease. Previous studies found that patients generally tolerate this treatment well. Reported side effects are mostly mild to moderate, such as injection site reactions or mild flu-like symptoms. Serious side effects have not commonly appeared in the research.
Since lonigutamab remains in early clinical trials, some uncertainty about its long-term safety exists. However, the data collected so far appears promising, showing potential without major safety concerns. Always consult a healthcare provider to understand what joining a trial might mean personally.12345Why are researchers excited about this trial's treatments?
Lonigutamab is unique because it targets the underlying cause of thyroid eye disease, potentially offering more precise treatment than traditional options like corticosteroids or radiation therapy. Unlike these standard treatments, which often address symptoms, lonigutamab is designed to be administered via subcutaneous injections, offering a potentially more convenient and patient-friendly delivery method. Researchers are excited about its ability to work on a molecular level, which could lead to better outcomes with fewer side effects.
What evidence suggests that this trial's treatments could be effective for Thyroid Eye Disease?
Research has shown that lonigutamab, a specially designed antibody, may help treat thyroid eye disease (TED). Early findings suggest it can greatly reduce eye inflammation and other symptoms of TED. In past studies, patients who received lonigutamab experienced significant improvements in their eye condition compared to before treatment. The evidence indicates that this treatment effectively targets and blocks IGF-1R, which plays a key role in TED. In this trial, participants will receive different doses of lonigutamab to evaluate its effectiveness. Overall, early results are promising for lonigutamab's ability to improve symptoms for those with TED.36789
Who Is on the Research Team?
Keenan, MD
Principal Investigator
ValenzaBio, Inc.
Are You a Good Fit for This Trial?
This trial is for men and women aged 18-70 with Thyroid Eye Disease (TED), showing eye protrusion and active symptoms within the last 15 months. Participants must have a Clinical Activity Score of at least 4, indicating active disease. They should not have had certain treatments for TED or conditions like inflammatory bowel disease, hearing loss, optic neuropathy, diabetes with high hemoglobin A1c levels, or recent steroid use.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive multiple doses of lonigutamab via SC injection, with varying schedules depending on cohort
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Placebo
- VB421
Find a Clinic Near You
Who Is Running the Clinical Trial?
ValenzaBio, Inc.
Lead Sponsor
ACELYRIN Inc.
Lead Sponsor