諦醫生技入圍世界ADC獎　技術平台與產品獲國際肯定

T-E Pharma宣布，旗下諦醫生技 (T-E Meds, Inc.) 成功入圍「第12屆世界ADC獎」之「2025 年最佳新藥開發者」獎項。諦醫生技從全球眾多競爭激烈的提名者中脫穎而出，成為全球僅六家的入圍公司之一，榮獲此項殊榮！

「世界ADC獎 (World ADC Awards)」自 2014 年創立以來，已成為全球抗體藥物複合物 (ADC) 領域最具指標性的國際獎項，象徵ADC技術創新、研發潛力與臨床價值的最高肯定。其中的「Best New Drug Developer」(最佳新藥開發者)，專門表揚ADC公司深具開發潛力且即將進入臨床的產品，肯定其在研發新穎性、差異化及實驗數據方面的優異表現。過程由業內資深專家評選，無論是入圍或獲獎，都象徵公司技術實力獲得國際認可，並展現其研發能力具備高度競爭力。

聚焦 ADC/ARC 創新研發，打造領先平台

諦醫生技是免疫功坊的姊妹公司，專注於抗體藥物複合物 (ADC) 與抗體放射性核種複合物 (ARC) 的創新開發。公司基於自主研發的「多臂鏈接體」(multi-arm linker) 技術平台，結合各式單藥或雙藥的藥物束 (mono- or dual-drug  bundle) 及模組化的偶聯反應，可用於開發各式兼具高藥物抗體比 (drug to antibody ratio; DAR)、高產率、高純度及靈活載藥潛力的新一代 ADC 藥物，打造獨有且具特色的國際級抗體偶聯藥物平台。

核心產品管線：TE-1146 與 TE-1182

· TE-1146：為全球首款將來那度胺 (Lenalidomide) 分子偶聯於抗CD38抗體 daratumumab的新型ADC藥物，有潛力治療多發性骨髓瘤與其它相關適應症。臨床前研究顯示，其腫瘤毒殺能力優於現有臨床藥物組合，能以更低劑量達到更佳治療效果，兼具高效能與高安全性。今年1月，公司已將TE-1146未來在台灣、東南亞及紐澳地區的商業化權利，以新台幣2.7億元授權予友華生技；接著6月更獲得台灣財團法人醫藥品查驗中心認證為「新藥開發指標案件」，充分展現市場價值與臨床發展潛力。目前已完成大部分CMC製程開發與前期毒理試驗，預計於2026年上半年提交新藥臨床試驗 (IND) 申請。

· TE-1182：是針對表達HER2之腫瘤 (如乳癌、胃癌、肺癌等) 所開發的雙載藥物 (dual-payload) ADC新藥，能克服腫瘤異質性與抗藥性挑戰，特別適用於 HER2 表現量較低或已產生抗藥性的後線治療。TE-1182不僅有潛力填補臨床用藥缺口，並為癌症病患提供更有效的治療選項。目前已完成多項關鍵研究，並持續推進臨床前評估，預計於2026年第四季提交IND申請，加速邁入臨床開發。

邁向全球舞台，推動突破性療法

諦醫生技此次入圍「第12屆世界ADC獎」之「2025年最佳新藥開發者」獎項，不僅展現公司在 ADC 創新技術與產品研發的堅強實力，更展現技術與產品具國際能見度與全球競爭力。公司將持續以先進平台技術推動候選藥物開發，致力為患者帶來更多突破性治療選擇，並加速臨床推進與全球市場布局。

World ADC Awards2025官網：https://worldadc-awards.com/about/2025-shortlist/

附表：諦醫生技領先 ADC 新藥開發管線：

聯絡資訊

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T-E Meds Shortlisted for World ADC Awards, Showcasing Global Recognition of Its Innovative Platform and Pipeline

T-E Pharma announced that its subsidiary, T-E Meds, Inc., has been shortlisted for the prestigious“Best New Drug Developer” category at the 12th World ADC Awards 2025. Selected from a highly competitive pool of global nominees, T-E Meds is one of six finalists to receive this distinguished honor.

Since its launch in 2014, the World ADC Awards has become the most influential international recognition in the field of antibody-drug conjugates (ADCs), honoring breakthroughs in innovation, R&D potential, and clinical value. The“Best New Drug Developer” award specifically acknowledges ADC companies with strong development potential and assets approaching clinical stages, highlighting excellence in innovation, differentiation, and experimental data. Being shortlisted itself reflects global recognition and affirms a company's competitive strength in ADC research and development.

Driving Innovation in ADCs and ARCswith a Leading Platform

T-E Meds, a sister company of Immunwork, is dedicated to the innovative development of ADCs andantibody-radionuclide conjugates (ARCs). Leveraging its proprietary multi-arm linker platform, the company integrates mono- and dual-drug bundles with modular conjugation chemistry to create next-generation ADCs. This platform enables product with a high drug-to-antibody ratio (DAR), high yield, high purity, and versatile payload capacity, establishing a distinctive and world-class ADC technology platform.

Core Pipeline Highlights: TE-1146 and TE-1182

· TE-1146:

TE-1146 is the first ADC linking lenalidomide to the anti-CD38 antibody daratumumab, developed for the treatment of multiple myeloma and related indications.  Preclinical studies have demonstrated superior tumor-killing efficacy compared with current drug combinations, achieving improved therapeutic outcomes at lower doses with both high potency and safety. In January 2025, T-E Meds out-licensed the commercial rights of TE-1146 in Taiwan, Southeast Asia,  Australia, and New Zealand to Orient EuroPharma for USD 8.5 million. In June 2025, the program was further recognized by Taiwan's Center for Drug Evaluation as “A Key New Drug Development Project”, underscoring its market value and clinical potential. With most of the CMC development and preliminary toxicology studies already completed, T-E Meds is targeting IND submission in the first half of 2026.

·  TE-1182:

TE-1182 is a dual-payload ADC targeting HER2-expressing tumors—including breast, gastric, and lung cancers—designed to overcome tumor heterogeneity and drug resistance, particularly in HER2-low or refractory settings. Addressing an urgent clinical need, TE-1182 aims to provide more effective therapeutic options for cancer patients.The program has completed multiple key preclinical studies and is advancing toward clinical readiness, with IND submission planned for Q4 2026.

Advancing Toward the Global Stagewith Breakthrough Therapies

T-E Meds' nomination for the 12th World ADC Awards – Best New Drug Developer underscores the company's robust innovation capabilities and growing global recognition in ADC technology and drug development. With its advanced platform and pioneering pipeline, T-E Meds remains committed to delivering breakthrough therapies, accelerating clinical advancement, and expanding its global footprint.

World ADC Awards 2025：https://worldadc-awards.com/about/2025-shortlist/

T-E Meds’ Leading ADC Pipeline:

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