Telix Announces Record-Breaking Presence at EANM 2025

MELBOURNE, Australia, Sept. 30, 2025 /PRNewswire/ -- Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, "Telix") today announces its record-breaking conference presence with 28 company-related abstract presentations at the 38^th Annual Congress of the European Association of Nuclear Medicine (EANM) to be held in Barcelona from 4 – 8 October 2025.

Dr. David N. Cade, Telix Group Chief Medical Officer, said, "We are pleased to showcase our late-stage and next generation development programs and innovations in MedTech at EANM – the largest gathering of nuclear medicine professionals worldwide. Telix presentation highlights include the Phase 3 ProstACT Global trial of TLX591 in mCRPC^[1], the IPAX-Linz and IPAX-2 therapeutic trials of TLX101 in glioma, and real-world experience with TLX250-CDx in ccRCC^[2]. Telix will host a sponsored symposium on CAIX^[3] and FAP^[4] targeting theranostics, and abstracts will also be presented from Telix's pan-tumor programs and its Rhine Pharma subsidiary, whose mission is to expand global access to innovative cancer imaging and therapy."

As in previous years, Telix will again support the EANM Sanjiv Sam Gambhir Young Investigator Award, in memory of an extraordinary man and an inspiring educator.

Visit booth #78 to explore opportunities for collaboration with Illuccix® (kit for the preparation of gallium-68 gozetotide injection) Telix's commercial PSMA-PET^[5] imaging agent in Europe, our industry-leading theranostic pipeline and 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: From pan-tumor innovation to theranostic precision . Fibroblast activation protein (FAP) and carbonic anhydrase IX (CAIX) case studies
Date & Time: 5-Oct-25, 13:15 – 14:45
Location: Room 116, CCI Barcelona
Chair: A. Italiano, Institut Bergonié (University of Bordeaux) & Gustave Roussy (Villejuif), France
Agenda:
Agnostic approaches in oncology and drug development: setting the stage

• A. Italiano

Introduction to FAP and diagnostic applications

• Y. Mori, Department of Nuclear Medicine, Medical Faculty and University Hospital Duesseldorf, Germany

FAP-targeted Radiopharmaceutical Therapy: A Promising Avenue in Radiomolecular Oncology

• R. Baum, CURANOSTICUM Wiesbaden-Frankfurt MVZ, Center for Advanced Radiomolecular Precision Oncology, DKD HELIOS Klinik, Wiesbaden, Germany

Clinical Applications of CAIX

• D. Oprea-Lager, Department of Medical Imaging, Radboud University Medical Center, Nijmegen, the Netherlands

Therapeutic potential of CAIX inhibitors

• C. Suárez, Vall d'Hebron University Hospital, Barcelona, Spain

Oral presentations

Title: Investigating FAP binding of the dimeric DOTAGA.Glu.(FAPI)₂ (TLX400) labelled with terbium-161 in ovarian cancer models incorporating the tumor microenvironment^[6]
Date and Time: 5-Oct-25, 15:10  – 15:20
Presenter: I. Primac, SCK CEN, Mol, Belgium
Abstract #: OP-150

Title: Reactive evaluation - a novel alternative to transfer learning to handle multi-centric variations in prostate cancer cohorts
Date and Time: 6-Oct-25, 09:45 – 09:55
Presenter: L. Papp, Medical University of Vienna, Vienna, Austria
Abstract #: OP-352

Title: Tumor-stroma dynamics define FAP optimum imaging and therapeutic windows in the management of glioblastoma
Date and Time: 6-Oct-25, 16:00 – 16:10
Presenter: A. Bilinska, Bern University Hospital, Bern, Switzerland
Abstract #: OP-417

Title: Synergistic anti-tumor effects of ²²⁵Ac-DOTA-girentuximab (TLX252) combined with DNA damage response inhibitors in CAIX-positive renal cancer
Date and Time: 7-Oct-25, 08:10 – 08:20
Presenter: Z. Cao, Olivia Newton-John Cancer Research Institute and Austin Health, Heidelberg, Australia
Abstract #: OP-516

Title: Integration of spatial analysis and deep learning for enhanced tumor classification in total-body PET/CT imaging: a preliminary study
Date and Time: 7-Oct-25, 08:50 – 09:00
Presenter: D. Han, Telix Pharmaceuticals, Sydney, Australia
Abstract #: OP-529

Title: Combining CAIX-targeted radionuclide therapy with immune checkpoint inhibitors: which inhibitor and when?
Date and Time: 7-Oct-25, 09:00 – 09:10
Presenter: S. Kleinendorst, RadboudUMC, Nijmegen, Netherlands
Abstract #: OP-521

Title: ProstACT Global: A Phase 3 study of lutetium (Lu177) rosopatamab tetraxetan (TLX591) plus standard of care vs standard of care alone in patients with metastatic castration-resistant prostate cancer
Date and Time: 7-Oct-25, 15:40 – 15:50
Presenter: J. Piulats, Bellvitge Biomedical Research Institute, Barcelona, Spain
Abstract #: OP-674

Title: Preliminary assessment of ⁸⁹Zr-Girentuximab (TLX250-CDx) excretion and radiation protection in ccRCC patients undergoing PET/CT imaging
Date and Time: 7-Oct-25, 17:35 – 17:45
Presenter: A. Piai, IRCCS Ospedale San Raffaele, Milan, Italy
Abstract #: OP-706

Title: IPAX-Linz: Phase 2 study to evaluate safety, tolerability, and preliminary efficacy of carrier-added ¹³¹I-IPA (TLX101) in patients with recurrent GBM concomitantly to 2nd line re-irradiation
Date and Time: 8-Oct-25, 08:00 – 08:10
Presenter: J. Pichler, Kepler University Hospital, Linz, Austria
Abstract #: OP-778

Title: Safety of radioligand therapy with ¹⁷⁷Lu-FAPi-Dimer (TLX400) with dose escalation in a clinical setting⁶
Date and Time: 8-Oct-25, 08:10 – 08:20
Presenter: J. Urena Poch, Rostock University Medical Center, Rostock, Germany
Abstract #: OP-779

Title: Immunomodulation of the tumor microenvironment by ²²⁵Ac-DOTA-girentuximab (TLX252) in a syngeneic murine tumor mode
Date and Time: 8-Oct-25, 09:10 – 09:20
Presenter: R. Ladjohounlou, University of Wisconsin, Madison, WI, U.S.
Abstract #: OP-767

Poster presentations

Title: Preclinical development of ¹⁶¹Tb-DOTA-HYNIC-panPSMA and comparison with ¹⁷⁷Lu-DOTA-HYNIC-panPSMA, ¹⁶¹Tb-DOTA-J591 and ¹⁷⁷Lu-DOTA-J591 (TLX591)
Presenter: C. Morgat, CHU Bordeaux, Bordeaux, France
Abstract #: EP-0069

Title: CAIX-targeting for radioimmunotherapy in triple-negative breast cancer
Presenter: A. Ivashkevich, Telix Pharmaceuticals, Melbourne, Australia
Abstract #: EP-0130

Title: Prostate cancer detection with ^99mTc-HYNIC-iPSMA SPECT: The Australian experience
Presenter: P. Tually, Spartan First Imaging, Kalgoorlie, Australia
Abstract #: EP-0353

Title: Potential of ⁸⁹Zr-girentuximab (TLX250-CDx) PET/CT for the routine clinical management of patients with suspicious, unspecified renal lesions (real-world experience)
Presenter: S. Rasul, Medical University of Vienna, Vienna, Austria
Abstract #: EP-0528

Title: Improving clinical management of von Hippel-Lindau Syndrome with ⁸⁹Zr-girentuximab (TLX250-CDx) PET Imaging (real-world experience)
Presenter: F. Gelardi, IRCCS Ospedale San Raffaele, Milan, Italy
Abstract #: EP-0534

Title: IPAX-2: Phase 1 safety and dose finding study of ¹³¹I-IPA (TLX101) plus standard of care in patients with newly diagnosed glioblastoma
Presenter: J. Pichler, Kepler University Hospital, Linz, Austria
Abstract #: EP-0785

Title: ¹⁷⁷Lu-DOTA-HYNIC-panPSMA radioligand therapy for patients with metastatic castration-resistant prostate cancer
Presenter: Y. Omar, Misr Radiology Center, Cairo, Egypt
Abstract #: EP-0810

Title: Robust self-supervised deep learning reconstruction model for reduced ⁸⁹Zr-girentuximab (TLX250-CDx) PET scan time
Presenter: C. Pain, Monash Biomedical Imaging, Melbourne, Australia
Abstract #: EP-0978

Title: Preclinical evaluation of DOTAGA.PEG₂.Glu.(FAPI)₂, a FAP dimeric inhibitor, for developing theranostic radiotracers in FAP-positive malignancies⁶
Presenter: N. Kumar, Bern University Hospital, Bern, Switzerland
Abstract #: EPS-013

Title: Intraindividual tumor dosimetry of monomer ⁹⁰Y-FAPI-46 vs dimer ⁹⁰Y-DOTAGA-Glu-(FAPI)₂ FAP radioligand therapy of advanced stage solid tumors
Presenter: P. Fragoso Costa, University Hospital Essen, University Duisburg-Essen, Essen, Germany
Abstract #: EPS-190

Title: Therapeutic potential of DOTAGA.Glu.(FAPI)₂ (TLX400) and DO3A.Glu.(FAPI)₂ with human dosimetry extrapolation for 177-lutetium and 161-terbium⁶
Presenter: A. Bilinska, Bern University Hospital, Bern, Switzerland
Abstract #: EPS-193

Rhine Pharma presentations

Title: Impact of formulation buffers on the radiolysis and stability of RHN001-Tx (¹⁸⁸Re-PSMA)
Date and Time: 6-Oct-25, 10:45 – 10:55
Presenter: S. Mdanda, Nuclear Medicine Research Infrastructure (NuMeRI), Pretoria, South Africa
Abstract #: OP-349

Title: Clinical trial protocol for RHINO trial: Prospective single-center Phase 1/2 study of RHN001-Dx/Tx in men with PSMA-positive prostate cancer post adjuvant androgen deprivation therapy and/or taxane-based chemotherapy
Date and Time: 8-Oct-25, 09:20 – 09:30
Presenter: H. Ndlovu, NuMeRI, Pretoria, South Africa
Abstract #: OP-825

Title: A comparative analysis of normal organ biodistribution and tumor uptake pattern of novel RHN001-Dx (^99mTc-PSMA) in correlation with tumor burden and its implications for theranostic use
Date and Time: 8-Oct-25, 11:05 – 11:15
Presenter: S. Martlbauer, University Hospital Dusseldorf, Heinrich-Heine-University Dusseldorf, Dusseldorf, Germany
Abstract #: OP-881

Title: A calibration workflow for accurate quantification of rhenium-188 in RHN001-Tx for theranostic applications
Presenter: M. Qebetu, NuMeRI, Pretoria, South Africa
Abstract #: EP-0942

Title: Quantitative ^99mTc-SPECT/CT dosimetry using a CZT gamma camera: Initial clinical experience
Presenter: K. Ramonaheng, NuMeRI, Pretoria, South Africa
Abstract #: EP-1116

Title: Production optimization and quality control testing of RHN001-Tx (¹⁸⁸Re-PSMA) per GMP standards
Presenter: S. Sibiya, NuMeRI, Pretoria, South Africa
Abstract #: EP-1200

About Rhine Pharma

Rhine Pharma™ is a wholly-owned subsidiary of Telix. Its mission is to expand global access to innovative cancer imaging and therapy by leveraging the unique benefits of technetium-99m (^99mTc) and rhenium-188 (¹⁸⁸Re).  Visit www.rhine-pharma.com for further information.

About Telix Pharmaceuticals Limited

Telix is a biopharmaceutical company focused on the development and commercialization of therapeutic and diagnostic radiopharmaceuticals and associated medical technologies. Telix is headquartered in Melbourne, Australia, with international operations in the United States, United Kingdom, Brazil, Canada, Europe (Belgium and Switzerland), and Japan. Telix is developing a portfolio of clinical and commercial stage products that aims to address significant unmet medical needs in oncology and rare diseases. Telix is listed on the Australian Securities Exchange (ASX: TLX) and the Nasdaq Global Select Market (NASDAQ: TLX).

Illuccix® (kit for the preparation of gallium-68 (⁶⁸Ga) gozetotide injection), Telix's first generation PSMA-PET imaging agent, has been approved in multiple markets globally. Gozellix® (kit for the preparation of gallium-68 (⁶⁸Ga) gozetotide injection) has been approved by the U.S. Food and Drug Administration (FDA). Telix's osteomyelitis (bone infection) imaging agent, technetium-99m (^99mTc) besilesomab, marketed under the brand name Scintimun®, is approved in 32 European countries and Mexico. Telix's SENSEI® drop-in gamma probe is registered with the Australian Therapeutic Goods Administration (TGA) and with the FDA and has attained a Conformité Européenne (CE) Mark for use in the European Economic Area. Telix's QDOSE® dosimetry software has received 510(k) clearance from the FDA and is CE-marked and Medical Device Regulation (MDR) certified for clinical use within the European Union (EU). No other Telix product has received a marketing authorization in any jurisdiction.

Visit www.telixpharma.com for further information about Telix, including details of the latest share price, announcements made to the ASX, investor and analyst presentations, news releases, event details and other publications that may be of interest. You can also follow Telix on X and LinkedIn.

Telix Investor Relations

Ms. Kyahn Williamson
Telix Pharmaceuticals Limited
SVP Investor Relations and Corporate Communications
Email: [email protected]

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