CLINICIAN-DESIGNED MULTIMODAL AI

A clearer view of changing prostate cancer risk.

OncoVera is developing VioPRO, an investigational multimodal AI system designed to bring quantitative prostate biopsy pathology together with MRI, PSA and clinical variables, and longitudinal follow-up to estimate the risk of clinically significant adverse reclassification during active surveillance.

Investigational · In Development

PATHOLOGY

MRI

PSA + CLINICAL

LONGITUDINAL

integrates into

VioPRO

Individualized risk estimate + contributing signals + change over time

THE CLINICAL DECISION

Active surveillance depends on recognizing when risk changes.

For appropriately selected men with localized prostate cancer, active surveillance can delay or avoid unnecessary treatment while preserving the option for curative treatment if the disease shows clinically important change.

The challenge is that evolving risk is reflected across multiple sources of information: biopsy morphology, PSA and PSA density, MRI findings, repeat biopsy results, and the patient's longitudinal clinical history.

VioPRO is being developed to bring these signals together around one clinically defined question: when does a patient who initially appears suitable for surveillance warrant closer reassessment?

OUR FIRST PRODUCT

VioPRO

Multimodal risk stratification for prostate cancer active surveillance.

VioPRO is OncoVera's first investigational product. It is being developed to support clinicians managing patients with apparently low-risk localized prostate cancer by estimating the probability of clinically significant adverse reclassification/progression over a defined time horizon.

The system combines quantitative pathology, imaging, structured clinical information, and longitudinal change in a single modeling framework.

Discover VioPRO

OncoVera

VioPRO

PATHOLOGY

Quantitative tissue phenotype

MRI

Imaging context

PSA + CLINICAL

Clinical context

LONGITUDINAL

Risk changes over time

Investigational · In Development

Four perspectives on one evolving disease.

PATHOLOGY

Quantitative tissue phenotype

Whole-slide prostate biopsy images are used to quantify clinically meaningful morphology selected with GU pathology expertise. The pathology representation can combine expert-defined quantitative features, conventional pathology variables, and complementary learned representations when they add reproducible value.

MRI

Imaging context

Structured multiparametric MRI information can include PI-RADS assessment, lesion characteristics, prostate volume, suspicion of extraprostatic extension, and longitudinal imaging change where available.

PSA + CLINICAL

Clinical context

PSA, PSA density, age, stage, biopsy history, prostate volume, and other routinely available clinical factors selected with clinical collaborators.

LONGITUDINAL

Risk changes over time

Serial PSA, repeat imaging, repeat biopsy findings, and relevant management events allow the model to incorporate change rather than rely on a single baseline snapshot.

VioPRO

Individualized risk estimate + contributing signals + change over time

Built around clinical meaning, not modality alone.

EXPERT-GUIDED PATHOLOGY

Pathology expertise defines the signal.

The pathology layer is not limited to generic image embeddings. Clinically meaningful tissue phenotypes are selected with GU pathology expertise and quantified at scale using whole-slide imaging AI.

MULTIMODAL BY DESIGN

The clinical picture is larger than the slide.

Pathology is combined with imaging, PSA and clinical variables, and longitudinal follow-up rather than treated as the entire prediction problem.

LONGITUDINAL RISK

Designed to evolve with the patient.

The architecture is intended to update risk as new PSA, MRI, and biopsy information becomes available.

INTERPRETABLE DEVELOPMENT

Designed to show what contributes.

Structured clinical variables and expert-defined quantitative pathology provide an interpretable foundation, while learned representations can be evaluated for incremental predictive value rather than treated as an opaque replacement for domain expertise.

Built for rigorous validation from the beginning.

Development is structured so that the pathology and multimodal workstreams can progress in parallel. Once a reproducible pathology representation meets predefined stability criteria, it can be versioned for multimodal modeling while pathology development continues underneath it.

01

PATHOLOGY REPRESENTATION

Define and quantify clinically meaningful prostate biopsy morphology.

02

MULTIMODAL MODELING

Combine pathology with clinical, MRI, and longitudinal data and measure the incremental contribution of each source.

03

VALIDATION

Perform patient-level temporal validation, external validation, calibration analysis, and component-level comparison.

04

TRANSLATION

Evaluate clinical workflow integration, regulatory strategy, reimbursement and economic value, and commercialization pathways.

Building VioPRO requires multiple clinical perspectives.

OncoVera is developing VioPRO through collaboration spanning GU pathology, urology, AI and engineering, biomedical informatics, and commercialization, with planned expansion of the platform into additional prostate cancer decision points.

We welcome conversations with clinicians, researchers, health systems, translational partners, and investors interested in advancing multimodal prostate cancer risk stratification.

Collaborate With Us
OncoVera

Developing clinician-designed multimodal AI for oncology risk stratification. VioPRO is our first investigational product for prostate cancer.

VioPRO and the OncoVera platform are investigational and are under development. They have not been cleared or approved by the U.S. Food and Drug Administration for clinical use. Information on this site is intended for research, collaboration, and educational purposes and does not constitute medical advice.

© 2026 OncoVera. All rights reserved.