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About
The overall objective is to study the safety, pharmacokinetics and efficacy of linsitinib (a small molecule IGF-1R inhibitor) administered orally twice daily (BID) vs. placebo, at 24 weeks in the treatment of subjects with active, moderate to severe thyroid eye disease (TED).
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Inclusion criteria
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Primary purpose
Allocation
Interventional model
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90 participants in 3 patient groups, including a placebo group
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Central trial contact
Robin Schmidt; Cathy Radovich
Data sourced from clinicaltrials.gov
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