AimedBio Announces Strategic Investment and Joint Research with AIVIS in AI-Based Biomarker Quantification

BioSpectator

February 3, 2026

AimedBio Announces Strategic Investment and Joint Research with AIVIS in AI-Based Biomarker Quantification

AI Quantification of ADC Nonclinical and Clinical Pathology Slides to Enable Biomarker-Based Patient Selection AimedBio announced on February 3 that it has entered into a joint research agreement with AIVIS, an AI-based digital pathology company, and completed a strategic equity investment (SI) to strengthen its antibody–drug conjugate (ADC) drug development capabilities. The size of the investment was not disclosed. Founded in January 2021, AIVIS provides AI-powered solutions that quantitatively analyze biomarker expression from digital pathology images to support clinical decision-making. The company was founded by a research team specializing in image processing and artificial intelligence at Korea University, led by CEO Daehong Lee, and includes Gyuyeong Kim, MD, former pathologist at Samsung Medical Center, as Chief Medical Officer (CMO). Through this collaboration, AimedBio will leverage AIVIS’s Qanti Discovery platform to apply AI-based quantitative analysis to pathology data generated during ADC development. The partnership aims to enhance the probability of clinical success by establishing biomarker-driven patient selection strategies. AimedBio plans to advance the collaboration in stages, focusing on automation of non-clinical and clinical pathology data analysis, improvement of patient selection precision, and development of an AI-based companion diagnostics (CDx) strategy. An AimedBio representative stated, “In the era of ADCs, AI-driven digital pathology and biomarker quantification capabilities are critical differentiators. Through this partnership, we aim to strengthen our data-driven drug development framework and enhance our clinical development competitiveness.” Qanti IHC, an AI-based medical device developed by AIVIS, enables cell-level quantitative analysis of IHC-stained slides. In September 2024, it received in vitro diagnostic medical device approval from Korea’s Ministry of Food and Drug Safety (MFDS). The solution is currently deployed in more than 10 major hospitals in Korea to support pathologists in improving diagnostic accuracy. AIVIS has continued to expand its strategic collaborations, including a licensing agreement with Philips Korea for AI-based cancer biomarker quantification solutions, as well as a memorandum of understanding (MOU) with AstraZeneca Korea last year to support the development of the domestic HER2 diagnostic ecosystem, including HER2 low.