This page shows the latest Teprotumumab news and features for those working in and with pharma, biotech and healthcare.
The US Food and Drug Administration (FDA) was due to deliver a verdict on Tepezza (teprotumumab-trbw) on 8 March. ... We believe teprotumumab may impact underlying mechanisms of fibrosis and could demonstrate utility beyond thyroid eye disease,
took intravenous teprotumumab meeting the primary endpoint of a 2mm reduction in eyeball protrusion, compared to 9.5% of the control arm. ... Teprotumumab has breakthrough therapy, orphan drug and fast track designations from the FDA.
Eye specialist Raymond Douglas of Cedars-Sinai Medical Centre in the US, one of the principal investigators in the trial, said that the reduction in proptosis with teprotumumab was “unprecedented”. ... If approved, teprotumumab would give physicians
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Another of its partners, Horizon Therapeutics recently submitted to the FDA the Genmab-developed teprotumumab for the treatment of active thyroid eye disease.
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