211-astatine-MX35 F(ab')2(Memorial Sloan-Kettering Cancer Center)

TOKYO--(BUSINESS WIRE)-- Sumitomo Heavy Industries, Ltd. (“SHI”) (TOKYO:6302) (Head Office: Shinagawa-ku, Tokyo, President and CEO: Shinji Shimomura) announced the decision to invest in Alpha Fusion Inc. (“AF”) (Head Office: Kita-ku, Osaka, Chief Executive Officer: Sunao Fujioka), a developer of Astatine based radiopharmaceuticals for Targeted Alpha Therapy (“TAT”). This press release features multimedia. View the full release here: Image Diagram of TAT (Graphic: Business Wire) AF will aim at establishing their pipeline (*1). Development of their radiopharmaceuticals is expected to be progressed by this funding and will lead more needs of Astatine-211. SHI is joining a new project led by Osaka University for mass production of Astatine-211 and will contribute for the development of the TAT, which is expected to be a future advanced medicine, with our technology of particle accelerators and a synthesis of radio-isotope (RI) labeled compounds. TAT and Astatine-211 TAT is a treatment that destroys cancer cells in the human body by injecting alpha emitting RI labeled candidate which selectively targets to cancer cells. Astatine-211 (211At, Atomic number 85, Half life time 7.2H) is an element belonging to halogens and has the property of emitting alpha particle. Due to no stable isotopes in nature, their properties have not been fully elucidated so far. However, it's getting attention in accordance with recent development of a nuclear medicine treatment and/or a theranostics (a new term combinated of therapy and diagnostic). Clinical studies had been already conducted in U.S. and Sweden etc. because of the advantages which is different from other approved RIs (177Lu, 223Ra, or 131I). The advantages are; stable production using naturally abundant bismuth (209Bi) with a relatively low-energy particle accelerator (cyclotron), short half-life time as 7.2 hours, and direct chemical formation with basic structure of candidates which conjugate with the disease target site. In Japan, investigator-initiated clinical trials targeting differentiated thyroid cancer (jRCT2051210144) at Osaka University and pheochromocytoma paraganglioma (jRCT2021220012) at Fukushima Medical University have started and further progress is highly expected. Alpha Fusion Inc. AF is a startup company who is conducting a social implementation of Astatine-211 based on drug discovery transferred research results of Osaka university funded by Program on Open Innovation Platform with Enterprises, Research Institute and Achademia (OPERA) promoted by Japan Science and Technology Agency (JST). In the field of targeted alpha therapy, which has been rapidly attracting worldwide attention in recent years, Mission of the company is to let the Astatine drug development out by using its originality from Japan in the field of TAT that is rapidly attracting worldwide attention. AF aims to lead this innovative modality into the basic of cancer treatment and are aiming at the practical application of new cancer treatment by proceeding with pipeline research and development to business development on a world-class level. Company Pro > Alpha Fusion Inc. Head office 2-5-13, Umeda, Kita-ku, Osaka, Japan Board of director CEO, Sunao Fujioka Business domain Technical research, drug discovery development, and business development of astatine-introduced compounds into a wide range of small molecules and antibodies, including Sodium astatide Capital 251 MJPY Web site (*1) Pipelines of AF are followings. Please refer to the URL for detail. • Pipeline 1 : Drug for thyroid cancer (Under Phase I clinical trial : ) • Pipeline 2 : Drug for prostate cancer (Preparing for clinical trial in next year : ) • Other 4 drugs are under development and preparing for a patent application for the basic technology View source version on businesswire.com: Contacts Sumitomo Heavy Industries, Ltd., Corporate Communication Department, +81-3-6737-2332 Alpha Fusion Inc., info@alpha-fusion.com Source: Sumitomo Heavy Industries, Ltd. Smart Multimedia Gallery Photo Image Diagram of TAT (Graphic: Business Wire) Logo View this news release and multimedia online at:

OPALESCENCE Phase II feasibility study of TLX250-CDx in patients with triple-negative breast cancer – early results suggest potential to detect carbonic anhydrase IX (CAIX) expression, theranostic potential in this difficult to treat disease. PERTINENCE Early Phase I feasibility study of TLX250-CDx in patients with non-muscle-invasive bladder cancer, a collaboration with ATONCO – early results support translation to first-in-human therapeutic studies with the alpha-emitting radioisotope astatine-211 (211At). Both investigator-initiated studies being undertaken by Dr. Caroline Rousseau at the Institut de Cancérologie de l'Ouest (ICO) in St Herblain (France). Results delivered at the European Association of Nuclear Medicine (EANM) Annual Congress currently taking place in Barcelona, Spain. MELBOURNE, Australia, Oct. 18, 2022 /PRNewswire/ -- Telix Pharmaceuticals Limited (ASX: TLX, Telix, the Company) today announces preliminary data from two separate investigator-initiated studies of TLX250-CDx (89Zr-DFO-girentuximab) in triple negative breast cancer (TNBC) and non-muscle-invasive bladder cancer (NMIBC), part of a comprehensive series of studies evaluating CAIX expression in cancers other than clear cell renal cell carcinoma (ccRCC), supporting Telix's goal to rapidly expand the CAIX program into other indications beyond kidney cancer. OPALESCENCE Phase II study of TLX250-CDx in triple-negative breast cancer reports preliminary data as a top-rated oral presentation at EANM The primary objective of OPALESCENCE (NCT04758780) is to evaluate how carbonic anhydrase IX (CAIX) targeting imaging with positron emission tomography (PET) can be utilised for the diagnosis and staging of triple-negative breast cancer (TNBC) and to develop a deeper understanding of CAIX as a potential therapeutic target in this patient population with a significant unmet medical need. Preliminary data demonstrates the feasibility of girentuximab to target CAIX expression in TNBC. Early results suggest potential for girentuximab as an imaging agent and therapeutic in this poor prognosis disease: 83% patient lesions had a CAIX strong expression allowing TLX250-CDx immunoPET detection, showing promise for further investigation. Three patients have all of their lesions detected by TLX250-CDx immunoPET. The best detected metastatic sites are bone. Based on these results, TLX250-CDx is an attractive novel investigative targeting agent for TNBC and potential alternative to biopsy and immunohistochemistry (IHC) for staging metastatic disease and targeted radioligand therapy. Should the targeting properties of this PET/CT imaging tracer be established in TNBC, Telix's intention is to broaden future applications for lutetium-177 and actinium-225 based CAIX therapies. Principal Investigator for the OPALESCENCE study, Dr. Caroline Rousseau stated, "We are pleased to announce preliminary results of this prospective pilot study of Telix's investigational CAIX ‑targeting imaging agent in TNBC. Early indications are that TLX250-CDx is showing promise as a diagnostic targeting agent in this disease, and we look forward to completing the study and presenting full results." Telix Chief Medical Officer, Dr. Colin Hayward stated, "Identifying new targets and treatment strategies for TNBC is a major unmet need, given the aggressive behaviour and distinct patterns of metastasis that characterise this cancer, and the lack of targeted therapies. Whilst a small patient population at this stage, early data from the OPALESCENCE study is encouraging as an indicator for future therapy applications of TLX250 and demonstrating the value of a "theranostic" approach" with this radiolabelled antibody. We would like to thank Dr. Caroline Rousseau and her clinical team at ICO for their commitment to this important study, and the patients who have contributed to date." PERTINENCE open-label, feasibility study of alpha therapy target reports preliminary data The objective of PERTINENCE (NCT04897763), an open-label, proof of concept study, is to evaluate safety profile, biodistribution and tumour targeting properties of TLX250-CDx given directly into the bladder in patients with NMIBC and to establish carbonic anhydrase IX (CAIX) as a potential therapeutic target in this condition. Preliminary data from this feasibility, dosimetry and imaging study at ICO,[1] shows encouraging tumour targeting and biodistribution with TLX250-CDx, and no systemic distribution of radiation. Based on these results, Telix's partner ATONCO intends to progress TLX250 labelled with the alpha-emitter astatine-211 (211At) into a first-in-human Phase I targeted alpha therapy (TAT) study. Patients with NMIBC currently have few therapeutic options with the risk of complete cystectomy (bladder removal). Therefore, new treatment options with preservation of the urinary bladder are urgently needed to address unmet medical need. Carbonic anhydrase (CAIX) is a cell surface protein that is highly expressed in many hypoxic solid tumours and a potential therapeutic target in NMIBC using a novel approach with TAT instilled directly into the bladder. This is aligned with Telix's strategy to develop diagnostics and radioconjugates as therapeutics with both alpha and beta emitters in new indications beyond kidney cancer. Alpha emitters such as 211At have the potential to deliver very high amounts of energy to cancer tissue whilst the short path length can decrease the risk of damage to surrounding healthy cells, increasing both the selectivity and potency of the radiation treatment. The prospective indications for alpha emitters are complementary to beta emitters due to their different properties: alpha therapies have a shorter penetration depth into tumours to suit smaller or disseminated tumours or micro-metastatic disease. Preliminary Results Four of six patients refractory to prior BCG therapy are included in current analysis: TLX250-CDx PET/CT showed intravesical radioactivity confined to the bladder and good tumour targeting. TLX250-CDx positivity was concordant to positive and negative immunohistochemistry results for CAIX expression. TLX250-CDx was well tolerated with an encouraging safety profile, suggesting feasibility for future alpha-immunotherapy development in patients with NMIBC. Principal investigator for the PERTINENCE study, sponsored by ICO, Dr. Caroline Rousseau said, "We are pleased to present preliminary data from this proof-of-concept study of TLX250-CDx in NMIBC. Early results for safety profile, biodistribution and dosimetry are encouraging and support translation to therapeutic studies with the alpha-emitting radioisotope astatine-211 (211At)." Telix Chief Medical Officer, Dr Colin Hayward and ATONCO Chief Medical Officer, Dr Jean-François Chatal together added, "These results are an important step towards using TLX250 with an alpha emitting isotope for the first time in humans." Dr Colin Hayward continued, "Telix is looking forward to continuing to support ATONCO in its development of 211At-labelled TLX250 for patients with NMIBC and establishing CAIX as a therapeutic target beyond kidney cancer in a series of important scientific studies." About Carbonic Anhydrase IX (CAIX) CAIX is a transmembrane protein that is highly over-expressed in clear cell renal cancer (ccRCC) as well as a number of other different cancer types, with very limited expression on normal healthy tissues, making it an attractive potential target for both new imaging and therapeutic modalities. Telix's core CAIX program is focused on ccRCC, the most common and aggressive form of kidney cancer, and is the subject of the ZIRCON Phase III (imaging) study, which recently completed enrolment,[2] and the STARLITE Phase II (therapy) studies.[3] In addition to OPALESENCE in TNBC, and PERTINENCE in NMIBC, a study targeting CAIX is also underway in urothelial carcinoma or bladder cancer,[4] with other collaborations being developed for ovarian, colorectal, head and neck, lung, and pancreatic cancers. About Triple-Negative Breast Cancer Breast cancer is the most common cancer in women and the second most common cancer overall.[5] In 2020, over 2.2 million women were diagnosed with breast cancer and 685,000 died from their disease.[6] Triple-negative breast cancer accounts for about 10-15% of all breast cancers with the term triple-negative referring to the fact that the cancer cells do not have any of the three markers commonly found on breast cancer cells – the oestrogen and progesterone receptors, and HER2 protein. TNBCs differ from other types of invasive breast cancer in that they grow and spread faster, have limited treatment options, and a poorer prognosis.[7] About Bladder Cancer Bladder cancer is the sixth most commonly occurring cancer in men, and the tenth most common cancer overall worldwide.[8] In 2020, 573,278 people worldwide were diagnosed with bladder cancer and 212,536 people died from their disease.[9] NMIBC is found in the tissue that lines the inner surface of the bladder and is responsible for approximately 75-85% of newly diagnosed bladder cancers.[10] About TLX250-CDx TLX250-CDx (89Zr-girentuximab) is an investigational product being developed by Telix for the purpose of non-invasive detection of ccRCC in patients with "indeterminate renal masses" (IDRMs). IDRMs are typically identified based on computed tomography (CT) or magnetic resonance imaging (MRI) and are an increasing medical dilemma as more scans are performed and more IDRMs are identified. Girentuximab is a monoclonal antibody that targets CAIX, a cell surface target that is highly expressed in several human cancers including renal, lung and oesophageal cancers. In July 2020, the U.S. Food and Drug Administration (FDA) granted Breakthrough Therapy (BT) designation for TLX250-CDx,[11] reflecting the significant unmet clinical need to improve the characterization of IDRMs previously identified on CT or MRI as ccRCC or non-ccRCC. TLX250-CDx does not currently hold a marketing authorisation in any jurisdiction worldwide. About the Institut de Cancérologie de l'Ouest (ICO) ICO is a 1,400 professional strong not-for-profit center fighting against cancer. It welcomes close to 48,000 patients per year, and conducts the mission and service of a public hospital. Strengthened by its 4 missions – Prevention, Care, Research and Teaching – ICO offers broad, state-of-the-art expertise that is exclusively dedicated to cancerology. The integration of care, research and innovation is integral to ICO. Research activities, which are a specific mission at ICO, are undertaken from concept all the way through to clinical trials. Research is conducted in all disciplines of cancerology: medical oncology, radiotherapy, surgery, anaesthesia, nuclear medicine, medical imagery, support care, and human sciences. Patients who are cared for at ICO receive privileged access to cutting edge clinical trials in cancerology. The Innovation Centre, opened in 2021, is dedicated to accompanying innovation in oncology, and thus supports internal and external projects, from concept, all the way to operational deployment. For more information contact: [email protected] About ATONCO ATONCO is a privately held French company that develops molecularly targeted radiopharmaceuticals for oncology applications. Originating from the world-class nuclear medicine cluster in Nantes, France, ATONCO and its partners are committed to the clinical use of alpha‑emitting radionuclides, in particular astatine-211 (²¹¹At). For more information visit or contact: [email protected] About Telix Pharmaceuticals Limited Telix is a biopharmaceutical company focused on the development and commercialisation of diagnostic and therapeutic radiopharmaceuticals. Telix is headquartered in Melbourne, Australia with international operations in the United States, Europe (Belgium and Switzerland), and Japan. Telix is developing a portfolio of clinical-stage products that aims to address significant unmet medical need in oncology and rare diseases. Telix is listed on the Australian Securities Exchange (ASX: TLX). For more information visit and follow Telix on Twitter (@TelixPharma) and LinkedIn. Telix's lead product, gallium-68 (68Ga) gozetotide (also known as 68Ga PSMA-11) injection, has been approved by the U.S. Food and Drug Administration (FDA),[12] and by the Australian Therapeutic Goods Administration (TGA),[13] and by Health Canada.[14] Telix Investor Relations Ms. Kyahn Williamson Telix Pharmaceuticals Limited SVP Corporate Communications and Investor Relations Email: [email protected] This announcement has been authorised for release by the disclosure committee of Telix Pharmaceuticals Limited. Legal Notices This announcement is not intended as promotion or advertising directed to any healthcare professional or other audience in any country worldwide (including Australia, United States and the United Kingdom). This announcement may include forward-looking statements that relate to anticipated future events, financial performance, plans, strategies or business developments. 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