Telix’s lead product for prostate cancer has been approved by the US FDA as a diagnostic agent for staging in newly diagnosed patients, or in patients with suspected recurrence.
More on our website: bit.ly/3s4baZa
Full prescribing information: bit.ly/3e7bPRG
Telix Pharmaceuticals
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Global biopharma company developing radiopharmaceuticals to address unmet medical need in oncology and rare diseases. ASX: TLX | NASDAQ: TLX
- Telix is pleased to today announce that the pivotal Phase III ZIRCON study of its investigational kidney cancer imaging agent TLX250-CDx has met its co-primary and key secondary endpoints, exceeding targets for sensitivity and specificity. More here: telixpharma.com/news-views/zir…
- We are pleased to announce the FDA has approved Telix's lead product as a diagnostic agent for prostate cancer, heralding a new era of patient and physician access to gallium-based PSMA-PET imaging. More on our website: bit.ly/3s4baZa #TelixPharma #PSMAPET #GalliumWave
- Telix has been jointly awarded a $5 million Australian Research Council (ARC) grant to establish a research hub for novel radiopharmaceuticals. Thanks to Prof Kristofer Thurecht at @UQ_News for leading a successful application and ARC for funding. More: bit.ly/3QtHhdE
- What a journey! The #EAU22 Telix PSMA symposium with Dr @CaPsurvivorship, Prof @stefanofanti4 & Prof Jochen Walz was an insightful discussion. Thank you to all the travellers who took part – with you onboard, the train is moving fast! Next stop: applying learnings to practice.
00:00 - The U.S. FDA has accepted Telix’sBiologics License Application (BLA) for its investigational kidney cancer imaging agent TLX250-CDx (Zircaix®, 89Zr-DFO-girentuximab), granting a Priority Review with a PDUFA date of August 27, 2025. This acceptance brings this breakthrough
- Today Telix officially joins the S&P/ASX 200 Index, effective prior to the open of trading. We would like to acknowledge the commitment of our staff, Board and partners, as well as the patients and investors who have supported Telix’s journey to date. #TelixPharma #ASX200
- Telix is delighted to announce the TGA has approved Illuccix® for prostate cancer imaging. We are especially pleased to receive our first regulatory approval in our home market, and look forward to bringing PSMA-PET imaging to patients across Australia. bit.ly/3wa3B3o
- Telix is excited to announce it has been named Australian Company of the Year in the 2022 @AusBiotech and @JNJInnovation Industry Excellence Awards. We are honoured to be recognised, and proud to be a part of Australia’s world-class life sciences sector. bit.ly/3TG4BHr
- Today, we formally welcome RLS Radiopharmacies into the Telix Group of companies, with the completion of the acquisition. This immediately enhances Telix’s presence in the United States (U.S.), with a network of over 30 radiopharmacies By uniting Telix’s industry-leading
00:00 - The FDA has approved Gozellix® (TLX007-CDx), Telix’s next-generation PSMA-PET imaging agent for prostate cancer. Gozellix® is a novel product with a longer shelf life and an extended distribution radius compared to existing gallium-based imaging products. The ability to
00:00 - Today marked an important milestone for Telix as we commenced trading on the @Nasdaq under the ticker “TLX”. We reaffirm our founding commitment to building a world-class global business, that delivers on the promise of precision medicine through targeted radiation, helping
GIF - In what is a major milestone for the company, Telix is delighted to announce that its first commercial New Drug Application for TLX591-CDx, for #ProstateCancer imaging, has been accepted for filing by the U.S. FDA. ASX release: bit.ly/3m047Ld #TelixPharma #SeeItTreatIt
- Telix is in Barcelona for this year’s EANM! Our symposium ‘Shifting perspectives in Genitourinary Oncology through nuclear medicine’ will take place on Sunday 16.10 from 13:15-14:45. See you there for what promises to be a fascinating discussion. bit.ly/3SRtorB #EANM22
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