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K-Pop Label MODHAUS Nets $15 Million Investment Before Boy Band Idntt
K-Pop Label MODHAUS Nets $15 Million Investment Before Boy Band Idntt

Forbes

timea day ago

  • Business
  • Forbes

K-Pop Label MODHAUS Nets $15 Million Investment Before Boy Band Idntt

The innovative structure of MODHAUS as a fan-participation music label and entertainment agency has secured it more than $15.1 million (₩21 billion) in investments after closing its Series B funding. Boasting girl groups ARTMS and tripleS, as well as the introduction of the first members of its new boy band, idntt, on August 11, the funding for MODHAUS marks the largest investment into a Korean entertainment company revealed in 2025 so far. South Korea's largest venture capital firm IMM Investment led this Series B funding round for MODHAUS. Three of Korea's other Top 10 VCs in Intervest, Smilegate Investment and LB Investment all joined too, with the former notable for being an early investor in HYBE. Meanwhile, existing investors such as Hedge Fund company Laguna Investment, the U.S.-based content venture capital firm Sfermion (who also recently backed U.S. K-pop company TITAN CONTENTS) and noted music NFT investor Cooper Turley followed up with additional backing. The funding is less about a traditional label model and more about a bet on a fan and platform-first strategy. Investors point to MODHAUS's Cosmo ecosystem — a direct-to-consumer fandom platform where fans vote on music releases, creative concepts and group units to influence the artists' content — as a scalable differentiator that turns fan armies into active partners in IP creation. To date, Cosmo reports accumulating roughly 350,000 users with about 150,000 monthly active users. Cosmo has also issued more than 10 million of its platform-exclusive digital photocards (what the company calls 'Objekts') representing its unique twist on K-pop fan behavior of buying multiple copies of album packages to collect more photocards. Since MODHAUS' launch in December 2021, the company has continuously made concrete traction with ultra-ambitious projects. tripleS's full, 24-member group album, ASSEMBLE25, was a commercial milestone for the company this spring with MODHAUS reporting 510,00 records sold in its first week for the group's fastest-selling release yet. Meanwhile, ARTMS has likewise broadened MODHAUS' global footprint since its 2024 debut with two world tours taking the quintet across Asia, North and South America, Europe and Australia. The timing of the capital raise comes just as MODHAUS is preparing to debut its first boy band idntt, a 24-member group operating on the same fan-participation principles of tripleS and ARTMS via Cosmo. The first 'unit' of idntt, named unevermet, consisting of seven members, will enter the K-pop industry on Monday, August 11, with a seven-track EP containing three singles 'BOYtude,' 'Storm' or 'You Never Met' to be voted on by fans and supporters as the album's 'super title song.' (At press time, three hours before the group's official debut, 'You Never Met' was the group's most-viewed music video teaser among the three.) What Will MODHAUS Do With Its New Investments? Jaden Jeong, CEO of MODHAUS and a longtime respected K-pop producer, shared in a press release that the Cosmo platform will expand more aggressively into international markets to reach its artists' global fandoms. Jeong described the latest company's creative ecosystem as 'a breakthrough for the global 'fandustry,' or fan + industry beyond just K-pop,' promising that its latest investments will 'refine that system further and take it to the next level.' Expanding more into what global projects fans can look forward to, Jeong tells Forbes exclusively that 'MODHAUS will continue to grow as a label specializing in large-member groups.' 'Having started in Korea, we are also preparing large-member groups in Japan and have begun discussions with the greater China region as well,' he adds. 'While our existing teams and new teams do not share a unified universe, launching new MODHAUS idols in various global markets allows us to introduce Cosmo in ways that match each region's unique color. This means that artists who share the DNA of MODHAUS can connect with fans around the world.' When asked if these latest investments will include additional international activities and opportunities for its artists, MODHAUS co-founder and vice president Joseph Baek shared additional insight. 'With this new investment, MODHAUS has secured a stronger financial foundation to pursue more aggressive global expansion,' Baek tells Forbes. 'ARTMS already has a large international fanbase and through the recent 'A Live 25' shows, the full 24-member lineup of tripleS met their Asian fans for the first time. Additionally, idntt is set to complete its 24-member lineup by the first half of next year and plans to launch large-scale promotions in partnership with a major global distributor. At such a crucial moment, we are pleased that this new investment will empower all our artists to push forward with greater momentum and scalability.' Notably, ARTMS' releases are distributed in the U.S. by Sony Music's independent arm The Orchard, bringing both the group's 2024 full-length album DALL and 2025 Club Icarus EP to major U.S. retailers and helping them land on Billboard's World Albums chart. Before MODHAUS' Series B investment round, its initial seed round was led by blockchain-specialized investment firm Hashed, with major Korean-entertainment players like Naver D2SF, CJ Investment and SM Culture Partners also joining as major investors. In July earlier this year, Jaden Jeong told Forbes that the company was actively hiring and 'needs more staff' beyond its 120 employees, hoping to find 'many people who are crazy about K-pop.'

ARTMS Drug Master File for Gallium Production Technology Referenced with Telix's Gozellix®
ARTMS Drug Master File for Gallium Production Technology Referenced with Telix's Gozellix®

Yahoo

time29-04-2025

  • Business
  • Yahoo

ARTMS Drug Master File for Gallium Production Technology Referenced with Telix's Gozellix®

BURNABY, British Columbia, April 01, 2025 (GLOBE NEWSWIRE) -- Telix ARTMS, Inc. (ARTMS), a global leader in radioisotope production technologies, is pleased to announce that the drug master file (DMF)1 for gallium-68 production using its QUANTM Irradiation System® (QIS®) cyclotron technology has been referenced for the first time with a United States (U.S.) Food and Drug Administration (FDA) approved product, with Gozellix® (kit for the preparation of gallium-68 (68Ga) gozetotide injection). This approval will enable radiopharmacies and hospitals using ARTMS' QIS® cyclotron technology and associated targets to produce multi-Curies of 68Ga for use with Gozellix®. The expanded distribution radius and increased dose production capacity, compared to existing gallium-based PET tracers, will facilitate broader and more equitable access. In addition, use of ARTMS' technology is being expanded internationally where regulatory submissions are in preparation. Pharmaceutical companies will be able to reference ARTMS' standardized isotope production technology with their approved drugs, helping to localize and simplify manufacturing. Chad Watkins, General Manager ARTMS and Isotope Strategy, Telix, said, 'This DMF reference represents a significant milestone for ARTMS, our partners and customers. The combination of these innovative technologies reflects Telix's commitment to working in partnership to reach more patients with 68Ga-PSMA-11, where and when they need it.' The QIS® forms part of ARTMS' 'turnkey' solution for customers that encompasses in-house manufactured targets and chemistry processing of isotopes, as well as DMF preparation and filing support. This makes large scale isotope production for hospitals and radiopharmaceutical distributors with cyclotrons significantly more attainable than with other existing technologies. ARTMS will continue to support the high efficiency, large-scale and cost-effective production of commercially important medical isotopes such as zirconium-89 (89Zr), gallium-68 (68Ga), technetium‐99m (99mTc) and copper-64 (64Cu), and will continue to partner with additional radiopharmaceutical companies to ensure that these critical isotopes are available on demand for patients. In addition, ARTMS' portfolio of advanced cyclotron technologies has application for Telix and select partners in the production of future commercially important alpha-emitting, therapeutic isotopes, including actinium-225 (225Ac) and astatine-211 (211At). For further information please contact: Chad Watkins Telix Pharmaceuticals LimitedGeneral Manager of ARTMS & Isotope StrategyEmail: Kevin ReimerTelix ARTMS, Global Sales and MarketingEmail: About Telix ARTMS, Inc. Based in Burnaby, British Columbia, Canada, Telix ARTMS, Inc. (ARTMS) is the global leader in the development of novel technologies and products which enable the high-quality and high-yield production of the world's most-used diagnostic imaging isotopes. ARTMS' flagship product, the QUANTM Irradiation System® (QIS®), enables decentralized, cost-effective, large-scale production of important medical isotopes such as gallium-68 (68Ga), zirconium-89 (89Zr), technetium‐99m (99mTc) and copper-64 (64Cu) using pharmaceutical distributor and hospital-based medical cyclotrons, empowering users to control their supply chain. ARTMS was acquired by Telix Pharmaceuticals in April 20242. For more information on QIS® and ARTMS, please follow us on X @ARTMS_TLX and LinkedIn and visit 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, 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. ARTMS, IsoTherapeutics, Lightpoint, Optimal Tracers and RLS are Telix Group companies. Telix is listed on the Australian Securities Exchange (ASX: TLX) and the Nasdaq Global Select Market (NASDAQ: TLX). Gozellix® (kit for the preparation of gallium-68 (68Ga) gozetotide injection) has been approved by the U.S. FDA3. Visit for further information about Telix, including details of the latest share price, ASX and SEC filings, investor and analyst presentations, news releases, event details and other publications that may be of interest. You can also follow Telix on LinkedIn, X and Facebook. Telix Investor Relations Ms. Kyahn Williamson Telix Pharmaceuticals Limited SVP Investor Relations and Corporate Communications Email: Legal Notices You should read this announcement together with Telix risk factors, as disclosed in our most recently filed reports with the Australian Securities Exchange (ASX), U.S. Securities and Exchange Commission (SEC), including our Annual Report on Form 20-F filed with the SEC, or on our website. The information contained in this announcement is not intended to be an offer for subscription, invitation or recommendation with respect to securities of Telix Pharmaceuticals Limited (Telix) in any jurisdiction, including the United States. The information and opinions contained in this announcement are subject to change without notification. To the maximum extent permitted by law, Telix disclaims any obligation or undertaking to update or revise any information or opinions contained in this announcement, including any forward-looking statements (as referred to below), whether as a result of new information, future developments, a change in expectations or assumptions, or otherwise. No representation or warranty, express or implied, is made in relation to the accuracy or completeness of the information contained or opinions expressed in the course of this announcement. This announcement may contain forward-looking statements, including within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, that relate to anticipated future events, financial performance, plans, strategies or business developments. Forward-looking statements can generally be identified by the use of words such as 'may', 'expect', 'intend', 'plan', 'estimate', 'anticipate', 'believe', 'outlook', 'forecast' and 'guidance', or the negative of these words or other similar terms or expressions. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance or achievements to differ materially from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking statements. Forward-looking statements are based on Telix's good-faith assumptions as to the financial, market, regulatory and other risks and considerations that exist and affect Telix's business and operations in the future and there can be no assurance that any of the assumptions will prove to be correct. In the context of Telix's business, forward-looking statements may include, but are not limited to, statements about: the initiation, timing, progress and results of Telix's preclinical and clinical trials, and Telix's research and development programs; Telix's ability to advance product candidates into, enrol and successfully complete, clinical studies, including multi-national clinical trials; the timing or likelihood of regulatory filings and approvals for Telix's product candidates, manufacturing activities and product marketing activities; Telix's sales, marketing and distribution and manufacturing capabilities and strategies; the commercialisation of Telix's product candidates, if or when they have been approved; Telix's ability to obtain an adequate supply of raw materials at reasonable costs for its products and product candidates; estimates of Telix's expenses, future revenues and capital requirements; Telix's financial performance; developments relating to Telix's competitors and industry; and the pricing and reimbursement of Telix's product candidates, if and after they have been approved. Telix's actual results, performance or achievements may be materially different from those which may be expressed or implied by such statements, and the differences may be adverse. Accordingly, you should not place undue reliance on these forward-looking statements. ©2025 Telix Pharmaceuticals Limited. Telix Pharmaceuticals®, Telix Group company, and Telix product names and logos are trademarks of Telix Pharmaceuticals Limited and its affiliates – all rights reserved. Trademark registration status may vary from country to country. _______________________ 1 A DMF is a submission to FDA used to provide confidential, detailed information about facilities, processes, or articles used in the manufacturing, processing, packaging, and storing of human drug products.2 Telix ASX disclosure 11 April 2024.3 Telix ASX disclosure 21 March in to access your portfolio

Telix Appoints Paul Schaffer as Chief Technology Officer
Telix Appoints Paul Schaffer as Chief Technology Officer

Yahoo

time06-04-2025

  • Business
  • Yahoo

Telix Appoints Paul Schaffer as Chief Technology Officer

MELBOURNE, Australia and INDIANAPOLIS, April 7, 2025 /PRNewswire/ -- Telix Pharmaceuticals Limited (ASX: TLX, NASDAQ: TLX, Telix, the Company) today announces that is has appointed Dr. Paul Schaffer to the newly created role of Chief Technology Officer (CTO), effective today. Dr. Schaffer has been CTO at ARTMS Inc. (ARTMS) (acquired by Telix in 2024) for the past seven years, as well as Director, Life Science at TRIUMF, Canada's particle accelerator research centre, since 2012. Based in Vancouver, Canada, Dr. Schaffer is widely recognized for his role in the buildout and transformation of the TRIUMF Life Sciences program, which included design and construction of a major multi-cyclotron radiochemistry facility and the development of the ARTMS QUANTM Irradiation System® (QIS®) for large-scale isotope production, which was commercialized and later acquired by Telix. As Telix CTO, Dr. Schaffer will be responsible for harnessing the power of technology to advance Telix's capabilities in radiopharmaceutical research, development, and clinical applications. Dr. Schaffer will cover areas including chemistry, physics, artificial intelligence (AI), dosimetry, and data analytics, complementing the work of Telix's Chief Scientist, Dr. Michael Wheatcroft, and his team in driving cutting-edge research and development (R&D). Dr. Schaffer said, "I'm excited to be taking on this role at such a pivotal time for Telix, as the Company advances rapidly toward its mission of transforming patient care. Telix has a bold commitment to innovation, and I'm thrilled to collaborate with this talented team to help drive R&D for the technologies behind the next generation of radiotherapeutics." Dr. Christian Behrenbruch, Telix Managing Director and Group Chief Executive Office, said, "Paul has an impressive track record of driving innovation in life sciences technology, including his groundbreaking work in large-scale isotope production. I have first-hand experience of Paul's impressive intellect, ideas and passion through his work at TRIUMF and with ARTMS, so it is a great pleasure to have him join the broader Telix team as we continue to lead radiopharmaceutical innovation." 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, 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. ARTMS, IsoTherapeutics, Lightpoint, Optimal Tracers and RLS are Telix Group companies. Telix is listed on the Australian Securities Exchange (ASX: TLX) and the Nasdaq Global Select Market (NASDAQ: TLX). Visit for further information about Telix, including details of the latest share price, ASX and SEC filings, investor and analyst presentations, news releases, event details and other publications that may be of interest. You can also follow Telix on LinkedIn, X and Facebook. Telix Investor RelationsMs. Kyahn WilliamsonTelix Pharmaceuticals LimitedSVP Investor Relations and Corporate CommunicationsEmail: Legal Notices You should read this announcement together with our risk factors, as disclosed in our most recently filed reports with the Australian Securities Exchange (ASX), U.S. Securities and Exchange Commission (SEC), including our Annual Report on Form 20-F filed with the SEC, or on our website. The information contained in this announcement is not intended to be an offer for subscription, invitation or recommendation with respect to securities of Telix Pharmaceuticals Limited (Telix) in any jurisdiction, including the United States. The information and opinions contained in this announcement are subject to change without notification. To the maximum extent permitted by law, Telix disclaims any obligation or undertaking to update or revise any information or opinions contained in this announcement, including any forward-looking statements (as referred to below), whether as a result of new information, future developments, a change in expectations or assumptions, or otherwise. No representation or warranty, express or implied, is made in relation to the accuracy or completeness of the information contained or opinions expressed in the course of this announcement. This announcement may contain forward-looking statements, including within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, that relate to anticipated future events, financial performance, plans, strategies or business developments. Forward-looking statements can generally be identified by the use of words such as "may", "expect", "intend", "plan", "estimate", "anticipate", "believe", "outlook", "forecast" and "guidance", or the negative of these words or other similar terms or expressions. Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, levels of activity, performance or achievements to differ materially from any future results, levels of activity, performance or achievements expressed or implied by these forward-looking statements. Forward-looking statements are based on Telix's good-faith assumptions as to the financial, market, regulatory and other risks and considerations that exist and affect Telix's business and operations in the future and there can be no assurance that any of the assumptions will prove to be correct. In the context of Telix's business, forward-looking statements may include, but are not limited to, statements about: the initiation, timing, progress and results of Telix's preclinical and clinical trials, and Telix's research and development programs; Telix's ability to advance product candidates into, enrol and successfully complete, clinical studies, including multi-national clinical trials; the timing or likelihood of regulatory filings and approvals for Telix's product candidates, manufacturing activities and product marketing activities; Telix's sales, marketing and distribution and manufacturing capabilities and strategies; the commercialisation of Telix's product candidates, if or when they have been approved; Telix's ability to obtain an adequate supply of raw materials at reasonable costs for its products and product candidates; estimates of Telix's expenses, future revenues and capital requirements; Telix's financial performance; developments relating to Telix's competitors and industry; and the pricing and reimbursement of Telix's product candidates, if and after they have been approved. Telix's actual results, performance or achievements may be materially different from those which may be expressed or implied by such statements, and the differences may be adverse. Accordingly, you should not place undue reliance on these forward-looking statements. ©2025 Telix Pharmaceuticals Limited. Telix Pharmaceuticals®, Telix Group company, and Telix product names and logos are trademarks of Telix Pharmaceuticals Limited and its affiliates – all rights reserved. Trademark registration status may vary from country to country. View original content to download multimedia: SOURCE Telix Pharmaceuticals Limited Sign in to access your portfolio

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