Telix Highlights Pivotal Trials in Prostate, Brain and Renal Cancers and Next Generation Theranostics at EANM

MELBOURNE, Australia and INDIANAPOLIS, Oct. 14, 2026 /PRNewswire/ -- Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, "Telix") today announces that 20 company-related abstracts will be presented at the 39^th Annual Congress of the European Association of Nuclear Medicine (EANM) to be held in Vienna, Austria from October 17-21, 2026.

Dr. David N. Cade, Telix Group Chief Medical Officer, said, "Our expansive presence at EANM reflects the breadth and maturity of Telix's pipeline, spanning pivotal therapeutic studies, precision diagnostics and next-generation technologies. The selection of 12 abstracts for top-rated oral presentations is a strong recognition of the quality and clinical relevance of this work. We look forward to continuing this discussion at our sponsored symposium on the future of theranostics in urologic oncology."

Key presentations include the Phase 3 IPAX BrIGHT trial of TLX101-Tx in recurrent glioblastoma, the Phase 3 LUTEON trial of TLX250-Tx in ccRCC, and interim results from the PTherpan-Lu trial of TLX597-Tx in mAPMR prostate cancer^[1]. Topline Phase 3 data for TLX591-Px (Illuccix) PET^[2] imaging of prostate cancer in Chinese men will also be presented, together with real-world experience with TLX250-Px (Zircaix^[3]) in ccRCC, and research from our targeted alpha therapy and MedTech programs. As in previous years, Telix will support the EANM Sanjiv Sam Gambhir Young Investigator Award, in memory of an extraordinary man and inspiring educator.

Visit booth #527 to explore opportunities for collaboration with Illuccix® (kit for the preparation of gallium-68 gozetotide injection), Telix's commercial PSMA-PET imaging^[4] agent in Europe; our theranostic pipeline; and our medical technologies, including the SENSEI® miniature drop-in gamma probe, QDOSE® dosimetry software and artificial intelligence (AI).

EANM presentation details are as follows (all times CEST): 

Sponsored Symposium

Title: The future doesn't wait: The next era of theranostics in urologic oncology.
Date & Time: 18-Oct-26, 13:15 – 14:45
Location: Hall F2, Austria Center Vienna
Chair: J. Calais, Gustave Roussy, IGR and Université Paris-Saclay, Paris, France
Agenda:
The theranostic revolution

• J. Calais

The evolving role of PSMA-PET in prostate cancer

• K. Herrmann, University Hospital Essen, Germany
• M. Ghesani, United Theranostics, USA

Next-generation PSMA therapeutics: Overcoming today's challenges

• D. Oprea-Lager, Radboud University Medical Center, Nijmegen, the Netherlands
• L. Emmett, St Vincent's Hospital, Sydney, Australia

Panel discussion - all

Extending prostate cancer theranostic success to broader GU diseases

• J. Calais

Oral presentations

Title: ELEGANCE, Prospective pilot study, assessing imaging performance of TLX250-Px ([⁸⁹Zr]Zr-girentuximab) PET/CT in Patients with Hepatocellular Carcinoma, Biliary Tract Cancer or Gastro-Entero-Pancreatic Neuroendocrine Neoplasms (NCT06735560)
Date and Time: 18-Oct-26, 08:00 – 09:30
Presenter: Clement Bailly, CHU Nantes
Abstract #: OP-036

Title: HIMIKO, TLX591-Px ([⁶⁸Ga]Ga-PSMA) PET/CT in Hepatocellular Carcinoma: impact of Multiparametric dynamic whole-body imaging and kinetic modelling (NCT06999837)
Date and Time: 18-Oct-26, 08:00 – 09:30
Presenter: Rachel Bardy, CHU Nantes
Abstract #: OP-041

Title: Exploring carbonic anhydrase IX as a diagnostic imaging target using TLX250-Px ([⁸⁹Zr]Zr-girentuximab) in Von Hippel-Lindau Disease: preliminary results from the CAT-VHL Phase 2 trial (NCT07171905)
Date and Time: 18-Oct-26, 15:00 – 16:30
Presenter: Fabrizia Gelardi, San Raffaele Hospital
Abstract #: OP-168

Title: LUTEON, Phase 3 study to assess safety and efficacy of TLX250-Tx (¹⁷⁷Lu-girentuximab) in advanced, relapsed or recurrent ccRCC (NCT07197580)
Date and Time: 18-Oct-26, 15:00 – 16:30
Presenter: Ghoufrane Tlili, CHU Bordeaux
Abstract #: OP-170

Title: Building the traceability backbone for radiopharmaceutical therapy, first results from the PDIB Secondary Standards Laboratory Network
Date and Time: 19-Oct-26, 08:00 – 09:30
Presenter: Steven Graves, University of Iowa
Abstract #: OP-291

Title: Optimizing SPECT/CT for alpha emitters: Phantom validation and calibration of [²¹¹At] imaging
Date and Time: 19-Oct-26, 08:00 – 09:30
Presenter: Rob van Rooij, UMC Utrecht
Abstract #: OP-294

Title: IODO-RISE, TLX101-Tx (iodofalan-¹³¹I) in recurrent high-grade glioma, investigation of safety and efficacy
Date and Time: 19-Oct-26, 08:00 – 09:30
Presenter: Tim Sturre, UMC Utrecht
Abstract #: OP-311

Title: IPAX BrIGHT, Pivotal study of TLX101-Tx (iodofalan-¹³¹I) with or without lomustine vs lomustine alone for the treatment of patients with radiographically confirmed recurrent glioblastoma at first recurrence (NCT07100730)
Date and Time: 19-Oct-26, 08:00 – 09:30
Presenter: Nelleke Tolboom, UMC Utrecht
Abstract #: OP-312

Title: Comparative evaluation of TLX252-Tx ([²²⁵Ac]Ac-) and TLX250-Tx ([¹⁷⁷Lu]Lu-DOTA-hG250) targeted radionuclide therapy and combination with PD1 blockade in a preclinical renal cell carcinoma model
Date and Time: 19-Oct-26, 16:45 – 18:15
Presenter: Twan van der Werff, UMC Radboud
Abstract #: OP-478

Title: Interim results from PTherpan-Lu trial: TLX597-Tx ([¹⁷⁷Lu]Lu-panPSMA) radionuclide therapy for patients with mCRPC^[5]
Date and Time: 19-Oct-26, 16:45 – 18:15
Presenter: Yehia Omar, Misr Radiology
Abstract #: OP-523

Title: Integration of spatial analysis and deep learning for enhanced tumor classification in total-body PET/CT imaging: using residual deep learning with spatial feature augmentation and cross-validated ensemble learning
Date and Time: 20-Oct-26, 09:45 – 11:15
Presenter: Simon Wail, Telix Pharmaceuticals
Abstract #: OP-613

Title: TLX250-Px ([⁸⁹Zr]Zr-girentuximab) PET/CT for characterization of indeterminate renal masses, diagnostic performance and clinical impact in a real-world cohort
Date and Time: 20-Oct-26, 09:45 – 11:15
Presenter: Sazan Rasul, Medical University of Vienna
Abstract #: OP-627

ePosters

Title: QDOSE® allometry-guided human dosimetry of TLX102-Tx ([²¹¹At]APA): Impact of administration route on maximum tolerated activity
Abstract #: EP-0067

Title: Illuccix China, preliminary results from Phase 3 trial of TLX591-Px (⁶⁸Ga-PSMA-11) PET for detection of biochemical recurrence of prostate cancer in Chinese men (NCT05847348)
Abstract #: EP-0460

Title: TLX250-Px (⁸⁹Zr-girentuximab) PET/CT in Von Hippel Lindau disease; initial real-world experience in VHL expert center
Abstract #: EP-0595

Title: TLX250-Px (⁸⁹Zr-girentuximab) PET/CT in clear cell renal cell carcinoma, impact on staging and clinical management
Abstract #: EP-0599

Title: Impact of TLX250-Px (⁸⁹Zr-girentuximab) based radionuclide imaging in patients with renal cell carcinoma on virtual tumor board decision making
Abstract #: EP-0606

Title: A semi-mechanistic population biodistribution model of TLX250-Px (⁸⁹zr-girentuximab) for the diagnosis of clear cell renal cell carcinoma
Abstract #: EP-0999

Title: Potential for radioguided surgery based on internal conversion electron detection using a compact CMOS detector
Abstract #: EP-1070

Title: A dosimetric study of bladder endocavitary therapy using astatine-211
Abstract #: EP-1239

About Telix Pharmaceuticals Limited

Telix Pharmaceuticals (ASX: TLX, NASDAQ: TLX) is a commercial-stage global radiopharmaceutical company, advancing targeted theranostics to improve outcomes for people with cancer across the patient journey. Theranostics pairs a precision diagnostic with a targeted therapy to both diagnose and treat disease. 

Telix's commercial franchise is anchored by its precision diagnostics portfolio: Illuccix® (kit for the preparation of gallium-68 gozetotide injection), commercially available in 22 countries including the U.S., and Gozellix® (kit for the preparation of gallium-68 gozetotide injection), approved by the U.S. Food and Drug Administration (FDA) for prostate imaging, and Pixclara® (floretyrosine F 18) approved by the FDA for glioma imaging. The Company's late-stage therapeutic pipeline includes three investigational assets in pivotal-stage trials: TLX591-Tx (lutetium-177 (¹⁷⁷Lu) rosopatamab tetraxetan) in prostate cancer, TLX101-Tx (iodofalan ¹³¹I) in recurrent glioblastoma, and TLX250-Tx (lutetium (¹⁷⁷Lu) girentuximab tetraxetan) in kidney cancer, additionally complemented by a deep pipeline of next generation candidates.

Telix is headquartered in Melbourne, Australia, with operations across North America, Europe, Latin America and Asia-Pacific. For more information, visit www.telixpharma.com or follow Telix on LinkedIn,X and Facebook.

Investor Relations

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Media

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