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Telix Doses First Patient in European TLX250-CDx Trial

Telix Doses First Patient in European TLX250-CDx Trial
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First Patient Dosed in European Named Patient (Early Access) Program for TLX250-CDx, Telix s Kidney Cancer Imaging Agent

Telix Reports Q1 2023 Financial Results: Delivers First $100M Revenue Quarter

Telix s ZIRCON Phase III Kidney Cancer Imaging Study Presented in Game Changing Session at EAU

MELBOURNE, Australia, March 14, 2023 /PRNewswire/ Telix Pharmaceuticals Limited (ASX: TLX, Telix, the Company) today announces additional positive results from its completed pivotal Phase III ZIRCON study of TLX250-CDx (89Zr-DFO-girentuximab) in clear cell renal cell carcinoma (ccRCC) (ClinicalTrials.gov Identifier: NCT03849118).1 The results were featured in a "Game Changing" oral session delivered by Professor Dr. Peter Mulders from Radboud University Medical Centre (Netherlands), a ZIRCON Principal Investigator, at the 38th Annual European Association of Urology (EAU) Congress, on Saturday, 11 March 2023. Game Changing sessions are reserved for Phase III trials or other developments that the EAU's Scientific Congress Office believes will have a large impact on daily practice. New data presented: TLX250-CDx demonstrated a high degree of consistency between readers with a very high sensitivity (85.5%) and specificity (87.0%) overall, and 85.5% / 89.5% for small masses

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