Intelligence from tissue to treatment

Leading life sciences organizations use Concentriq, our pathology AI platform, to turn tissue into actionable biomarkers, raise the probability of clinical success, and reach more patients.

Precision medicine runs on pathology

>300

 investigational ADCs in the pipeline¹

36%

of FDA-approved therapies are personalized medicines²

20%

of patients respond to immune checkpoint inhibitors, leaving a wide unmet need³

2x

higher likelihood of approval with biomarker-driven trials⁴

75%

of FDA-approved CDx rely on tissue-based testing⁵

Discover, Develop, Deliver

Discover reliable biomarkers in a fraction of the time, run successful trials across global sites, and take an AI CDx from research to deployment on one platform. Start where your program needs Concentriq today.

BIOMARKER DISCOVERY

Turn tissue into reliable biomarkers faster

Move quickly from early signals to confident program decisions.

Microscopic image showing PD-L1 high expression in tumor cells with analysis and a bar chart of treatment response rates.
Move at the speed of your questions

With frontier pathology models built in, agentic biomarker discovery tools let scientists test hypotheses, analyze images, and assess biomarker performance in hours, not weeks.

Validate hypotheses against
real-world cohorts

Interrogate biomarker algorithm performance with real-time access to diverse de-identified patient populations from a global lab network powered by Aperture, Proscia’s real-world multimodal data.

Build a rich data foundation

Clinical and translational data flows back into discovery, sharpening every next hypothesis. Teams and partners move faster on one searchable, intelligent, and open data layer.

“We're no longer talking about potential. We're talking about real tangible impact. We’re seeing firsthand how computational pathology on Concentriq is influencing early decision making, biomarker strategy, and even clinical trial design.”

CLINICAL DEVELOPMENT

Increase the probability of clinical trial success

Leading CROs and clinical development teams move programs forward faster, at a lower cost and risk.

Design with confidence

Use real-world data to characterize biomarker prevalence, model cohort feasibility, and identify the sites best positioned to recruit your population.

Operate global trials at scale

Centralize slides across trial sites to build consensus faster, standardize scoring with AI, and produce defensible, reproducible data.

Enrich for likely responders

Hit enrollment goals faster by pre-screening patients with algorithms that predict biomarker expression before expensive profiling6.

“Standardization [on Concentriq] aids in patient enrollment in clinical trials, stratification, randomization into treatment arms and endpoint evaluation.”6

COMPANION DIAGNOSTICS

Reach the patients your therapy is meant to find

Leverage a regulated platform and global lab network to build, validate, and deploy CDx and biomarkers into routine clinical use.

Build and validate assays
Access multimodal real-world data to iterate on assays, assess performance, and generate evidence for regulatory approval.

Deploy where patients are diagnosed
With millions of patient cases diagnosed each year across academic, reference, and health systems, Concentriq is uniquely positioned to support scalable biomarker and companion diagnostic deployment.

User interface screen showing PD-L1-NSCLC tumor analysis with image overlay of highlighted tumor nuclei.

Multimodal data ready to advance your program.

Proscia Aperture brings real-world data into Concentriq as cohorts or real-time insights. Access AI-enriched tissue images, molecular, clinical, and genomic data derived from nearly 4,000 hospitals and clinics.

Specimens span the full diagnostic journey — diagnostic biopsy, surgical resection (lumpectomy and mastectomy), lymph node, and metastatic sites

Hormone receptor and HER2 status (ER, PR, HER2) for treatment stratification research

Proliferation and lineage markers (Ki-67, GATA3, E-cadherin) for tumor characterization and subtype differentiation

NGS testing available, with tumor cellularity data linked at the patient level

Specimens span the disease course — needle biopsy, TUR, radical prostatectomy, lymph node, and metastatic sites including bone

Androgen pathway and lineage markers (PSA, NKX3-1, ERG) for prostate-specific tumor characterization

PTEN and neuroendocrine markers (SYNAP, CHROMOGRANIN) for aggressive and variant disease research

NGS testing available, including TP53 and RB1 mutation status, linked to tested patients

Specimens include primary ovarian and uterine tumors, metastatic sites, and non-neoplastic tissue for comparative research

Müllerian lineage markers (PAX8, WT-1) for ovarian tumor characterization

ADC target markers (FOLRA) alongside HER2 for targeted therapy research

MMR panel (MLH1, MSH2, MSH6, PMS2) with NGS testing available, including TMB and MSI status

Specimens span the full biopsy spectrum — transbronchial, lung, and lymph node biopsies, FNA, and surgical resection

Lineage markers (TTF-1, NAPSIN, P40, CK7) for histologic subtyping

Targetable pathway markers (CMET, PD-L1) for actionable biomarker research

NGS testing available, including TMB and MSI status with a large TMB-High population

Specimens span dermatopathology and soft tissue workflows — shave, punch, excision, sentinel node, and mass biopsy

Melanocytic lineage markers (Melan-A, SOX10, HMB45) for melanoma characterization

PRAME as a diagnostic and prognostic adjunct for melanoma, with epithelial markers (AE1AE3, BEREP4) for carcinoma differentiation

NGS testing available, including a strong TMB-High population across melanoma and non-melanoma subtypes

Trusted by 16 of the top 20
pharma companies and leading CROs

Concentriq is the platform scienctis love, program managers trust, and leadership backs.

"The ultimate goal is to find the right patient for the right treatment. We are trying now to identify one that will be eligible for a specific treatment — and greatly benefit from it."

Built for the way life sciences works

Computational pathology designed to scale technically, operationally, and in regulated environments.

The intelligence is in the tissue

Connect with a life sciences expert to learn how Proscia can help your organization tackle modern R&D's biggest challenges.

¹ Topol E. The Remarkable Proliferation of Cancer Immunotherapies. Ground Truths. Published May 2026. Accessed June 15, 2026.
² Personalized Medicine Coalition. Personalized Medicine at FDA: The Scope & Significance of Progress, 2025. Published 2025. Accessed June 15, 2026.
³ Haslam A, Olivier T, Prasad V. How many people in the US are eligible for and respond to checkpoint inhibitors: an empirical analysis. Int J Cancer. 2025;156(12):2352-2359. doi:10.1002/ijc.35347
⁴ Biotechnology Innovation Organization; Informa Pharma Intelligence; QLS Advisors. Clinical Development Success Rates and Contributing Factors, 2011–2020. Published February 2021.
⁵ U.S. Food and Drug Administration. List of cleared or approved companion diagnostic devices (in vitro and imaging tools). Updated continuously.
Use of AI algorithms for live patient screening, stratification, or enrollment must be conducted under an approved investigational protocol or validated in accordance with applicable regional regulations.

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