Roche (RHHBY) presented at ASPORS meeting primary results of the Phase 3 SatraGO-1 and SatraGO-2 trials — Efficacy and Safety of Satralizumab in Thyroid Eye Disease. The SatraGO-1 study in active TED failed to meet its primary endpoint — proptosis response at week 24 — with placebo-adjusted rates of 18%-30%. The SatraGO-2 study met its primary endpoint of proptosis response — 53% vs. 23%. The company said that “Satralizumab showed clinically meaningful improvements across key efficacy endpoints, including proptosis, diplopia, and CAS inactive TED. The safety profile of satralizumab in TED was highly favorable, with no reports of AEs commonly associated with other treatments for TED.”
Elevate Your Investing Strategy:
- Take advantage of TipRanks Premium at 50% off! Unlock powerful investing tools, advanced data, and expert analyst insights to help you invest with confidence.
Published first on TheFly – the ultimate source for real-time, market-moving breaking financial news. Try Now>>
Read More on RHHBY:
- Underwhelming Roche data helps Veridian’s position in TED, says Jefferies
- Merck KGaA Joins Price Cut Agreement with Trump to Dodge Tariffs
- CHMP recommends EU approval of Roche’s Gazyva/Gazyvaro for lupus nephritis
- Roche announces Direct-to-Patient program for Xofluza
- Roche says FDA clears Elecsys pTau181 test