AIM-CD3
Automated CD3+ cell assessment for celiac disease
Company profile
Company profile
PathAI is dedicated to improving patient outcomes with reliable AI-powered technology and meaningful collaboration with biopharma and pathology laboratories.
Company description PathAI official website
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01 · Operating footprint
Company-profile context for clinical focus, customers, deployment, integration, milestones, and partnerships.
Cloud Saas deployment with recorded integration context.
Company milestones
PathAI entered definitive merger agreement to be acquired by Roche (2026). FDA clearance for AISight Dx Platform for primary diagnosis (June 2025). FDA Qualification for AIM-MASH AI Assist (December 2025). Expanded collaboration with Labcorp (February 2026). Partnership with MedStar Health (April 2026). Launch of AIM-HI UC and IBDExplore (February 2026).
Partnerships
02 · Flagship portfolio
Selected source-backed Company products and the available commercial context.
Automated CD3+ cell assessment for celiac disease
Automated Geboes scoring for ulcerative colitis
AI-based measurement panel for breast cancer biomarkers
FDA-qualified AI tool for MASH clinical trials
AI-powered PD-L1 biomarker detection and quantification
Automated tumor-cellularity assessment for molecular testing
AI-enabled clinical development platform for biopharma trials
Pathology consultation services integrated with digital pathology
FDA-cleared digital pathology platform for primary diagnosis
03 · Research intelligence
Publications, preprints, clinical validation, and regulatory records in Evidence Position order.
Publications, clinical validation, and regulatory records connected to this Company appear here.
Research
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · Jul 24, 2026
Comparative in vitro evaluation of fourth-generation anti-GPC3 CAR T-cells in hepatocellular carcinoma.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · Jul 6, 2026
Machine Learning Assessment of Pathologic Response in Lung Cancer Resections After Neoadjuvant Therapy-IASLC MPR Project.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · Jun 1, 2026
CD138-targeted bispecific protein engager-armed T cells exhibit potent and selective cytotoxicity against multiple myeloma cells.International immunopharmacology · Apr 1, 2026
Enhanced antitumor efficacy of next-generation B7-H3 chimeric antigen receptor T cells containing CD28, CD137 and CD27 costimulatory domains in multiple myeloma.Cytotherapy · Mar 1, 2026
Self-differentiated Dendritic Cells Presenting NY-ESO-1 Prime Cytotoxic T Cells for the Treatment of Multiple Myeloma.Anticancer research · Jan 1, 2026
Clinical validation
No linked records are currently available.
Regulatory
No linked records are currently available.
04 · Company-reported outcomes
Company-reported outcomes and customer stories are distinct from linked Research Intelligence evidence.
in proprietary pathologist contributor network
contributed for AI algorithm training and validation
leverage PathAI technology
Deploy AISight Dx Digital Pathology Platform and advanced AI applications for anatomic pathology
Nationwide deployment of FDA-cleared digital pathology platform
05 · Leadership
Leadership profiles and professional links from the current Company record.
No active leadership profiles are currently listed.
06 · Company updates
Recent articles published on PathAI's official website.
07 · HAIC coverage
Health AI Central reporting that mentions this Company.
No HAIC coverage is currently linked to this Company.
08 · Official presence
Curated official destinations from the active Company record.
09 · Market pathway
Other active Companies in the same market, selected alphabetically from the HAIC directory.
Market context
Companies applying AI to digital pathology, histopathology slide analysis, laboratory diagnostics, or biomarker discovery. Includes AI-powered interpretation of lab test results, at-home diagnostic devices with AI analysis, and platforms that analyze tissue samples or biological specimens to support clinical diagnosis.
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Linked research, clinical, and regulatory source pathways.
Expanded product, deployment, integration, and partnership research.
Record-level provenance and review context.