Expertise that connects.
Founders spanning machine learning, retinal disease, and clinical innovation. Different disciplines, united by questions that matter to patients.
Turning retinal imaging into predictive insight—for more precise research, better-informed trials, and a future of earlier, individualized care.
Clinically grounded. Research driven. Built for collaboration.
HealthLadder.AI brings together clinical insight, machine learning, and ophthalmic research to understand not only where disease is—but where it may be going.
Founders spanning machine learning, retinal disease, and clinical innovation. Different disciplines, united by questions that matter to patients.
A research foundation in predictive algorithms and imaging biomarkers, with an initial focus on progression from intermediate AMD to geographic atrophy.
Who may progress? When might it happen? How can better evidence inform clinical trials and the development of more individualized treatment?
Our development approach connects ophthalmic imaging, predictive modeling, and clinical interpretation. The goal: useful insight that can be evaluated in real research workflows.
Use OCT imaging to study retinal structure, with multimodal research opportunities across fundus images and clinical measures.
Explore signals associated with disease progression through multi-scan modeling and attention-based interpretation.
Evaluate progression risk, trial-enrichment strategies, and the potential for earlier intervention research.
Retinal imaging provides the starting point for investigating how structural patterns relate to future disease progression.
Conceptual illustration. Not patient data, a product interface, or live AI output.
Connecting the people who understand disease with those developing the next generation of care.
We are advancing research that connects retinal imaging to clinically relevant questions about progression, timing, and patient selection.
Examine the evidenceInvestigate which eyes with intermediate AMD may develop geographic atrophy.
Study lead time and the distinction between early disease detection and true prediction.
Prioritize independent testing, device-aware evaluation, and subgroup analysis.
Explore predictive biomarkers to inform trial-enrichment strategies and investigate treatment response, dose, and interval questions in therapeutic development.
Explore collaboration modelsEvaluate whether imaging-derived risk can identify participants relevant to a study’s progression endpoint.
Align prediction horizons with a therapeutic program’s biological rationale and clinical objectives.
Connect structural and functional outcomes to the development of more individualized therapies.
A clinician-informed AI approach with opportunities spanning sponsored validation, algorithm licensing, and development partnerships—plus selective investment and acquisition discussions.
Explore the strategic opportunityLead with a defined question in AMD progression rather than an undifferentiated AI platform.
Link expansion to validation results, data permissions, deployment feasibility, and clinical relevance.
Bring together an AI team, a research and IP foundation, and clinical translation expertise.
Research priorities and future directions—not a list of approved or commercially available indications.
Our approach starts with published science—and advances through careful, use-case-specific evaluation.
A retrospective study investigated whether volumetric OCT could predict progression from intermediate AMD to geographic atrophy over approximately one year.1
These are retrospective research results, not prospective clinical-outcome claims or guaranteed product performance. AUROC measures discrimination; it is not the percentage of patients correctly classified.
Read the publication (opens in a new tab)| Cohort | Patients | Role in the study |
|---|---|---|
| AREDS2 A2A | 316 | Development and cross-validation |
| Routine-care cohort 2 | 53 | Independent validation |
| Routine-care cohort 3 | 48 | Independent validation |
The validation cohorts used Heidelberg Spectralis images; the development cohort used Bioptigen images. Validation AUROCs differed across cohorts: 0.94 and 0.84, respectively.1
What comes next: prespecified, blinded studies that test performance in the intended population, distinguish baseline atrophy markers from future progression, and evaluate sensitivity across clinically relevant lead times.
Why it matters: a promising retrospective model is a foundation for further evaluation—not evidence that a particular treatment, dosing strategy, or deployment improves patient outcomes.
1. Dow ER, Jeong HK, Katz EA, et al. Prediction of near-term geographic atrophy from SD-OCT. JAMA Ophthalmology. 2023;141(11):1052–1061. doi:10.1001/jamaophthalmol.2023.4659 (opens in a new tab)
A founding team connecting artificial intelligence, ophthalmic research, and the work of translating ideas into meaningful clinical progress.
PhD
Connecting advanced machine learning with the challenges of building useful, clinically relevant AI.
MD, PhD
Bringing retinal disease, imaging biomarkers, and therapeutic-development questions into focus.
MD, PhD
Uniting clinical innovation, company building, and strategic collaboration to move research forward.
HealthLadder.AI is an independent Duke spinout. Academic affiliations describe the team’s scientific roots and do not imply institutional endorsement.
Explore the fit between your capabilities and ours—from focused validation and co-development to licensing, strategic investment, and acquisition opportunities.
Explore trial enrichment, predictive biomarkers, and research into earlier intervention and individualized treatment.
Investigate device-specific validation, research workflow integration, and routes from imaging to predictive insight.
Evaluate investment, licensing, and strategic transactions around a complementary team, research foundation, and clinical vision.
Progress with clarity. A productive partnership starts with a defined clinical question, documented rights, measurable milestones, and a shared decision about what to do next.
How we think about the science, the opportunity, and the path ahead.
Our initial focus is predictive research in age-related macular degeneration, particularly progression from intermediate AMD to geographic atrophy. Broader research directions include imaging biomarkers, fibrosis, and treatment response. Oculomics—the study of ocular features as signals of wider health—is a longer-term direction, not a claim of established systemic-disease detection.
This website describes research and development activities, not an offer of an approved diagnostic or treatment product. Published findings do not establish authorization for routine clinical use. Any deployment requires an appropriate intended use, study approvals, and applicable regulatory review. The visualizations here are illustrative, not clinical outputs.
Potential structures include sponsored evaluation, algorithm licensing, biomarker co-development, and research integration. The right model depends on the clinical question, evidence requirements, data permissions, and each party’s responsibilities. Investment and acquisition opportunities can be evaluated separately where there is a strong strategic fit.
No. University research, institutional datasets, and company capabilities are distinct. Data access, licensing scope, publication rights, and any transfer of intellectual property must be established in the relevant agreements and institutional approvals. A relationship with HealthLadder does not itself confer access to Duke data or technology.
Bring scientific possibility and clinical purpose into the same field of view.
Explore strategic opportunitiesCo-founder / AI & machine learning
Larry’s contribution to HealthLadder connects machine-learning research with the practical challenge of developing predictive models for clinical applications.
Lawrence Carin is a co-author of the foundational 2023 DeepGAze publication. His work connects algorithm development, model evaluation, and the path from research to application.
Co-founder / Ophthalmic clinical science
Nora brings a retinal-disease and clinical-research perspective to the questions HealthLadder is working to answer: who may progress, when progression may occur, and how better evidence can inform therapeutic development.
Eleonora M. Lad is a co-author of the foundational 2023 DeepGAze study and the intermediate AMD biomarker review listed in the scientific references.
Co-founder / Translation & strategy
Nandan’s role connects clinical innovation, company development, and strategic collaboration. The focus is translating research into opportunities that are scientifically grounded and commercially coherent.
Clinical translation begins with a defined use case, a credible evidence plan, and aligned development priorities.
Potential collaboration / Pharma & biotech
Explore how predictive imaging research could complement a therapeutic development program, beginning with a focused, testable use case.
Define the endpoint and prediction horizon, establish permissions, lock the evaluation plan, and conduct a blinded assessment. Consider broader licensing or co-development only after reviewing the evidence.
These are potential collaboration structures, not announcements of existing commercial agreements or established clinical efficacy.
Potential collaboration / Imaging & technology
Build a research program around the imaging and workflows your organization already understands.
Image-format support, cloud architecture, operational responsibilities, and validation requirements should be established together. No universal device compatibility or live vendor integration is implied.
Device and technology partnerships require separate agreements; no technology vendor is represented as an endorsed or confirmed partner on this site.
Strategic opportunity / Investment & transactions
HealthLadder welcomes consideration of strategic structures that connect its founding expertise and research direction with complementary development, distribution, or capital capabilities.
Team and execution capacity; model versions and evidence; intellectual-property ownership and licensing; data provenance and permissions; regulatory strategy; and potential commercial economics.
No valuation, fundraising terms, guaranteed return, or availability of third-party data is represented here. This is an invitation to evaluate strategic fit, not an offer to sell securities.
Our partnership framework
Agree on the intended use, target population, endpoint, prediction horizon, and measurable acceptance criteria.
Document the applicable data permissions, model license, field of use, site and vendor scope, publication rights, and institutional approvals.
Lock the model and analysis plan. Use blinded scoring, untouched test data, confidence intervals, and relevant subgroup analyses.
Review clinical relevance, technical feasibility, and commercial fit. Expand only where the evidence supports the next phase.
A phased evaluation does not presume a successful result or create an automatic obligation to proceed with a broader transaction.
Selected scientific foundation
Predicting near-term geographic atrophy from OCT.
Dow ER, Jeong HK, Katz EA, et al. JAMA Ophthalmology. 2023;141(11):1052–1061.
Open the publication ↗ (opens in a new tab)Source for the retrospective study metrics and cohort descriptions presented on this site.Biomarkers in intermediate AMD progression.
Lad EM, Finger RP, Guymer R. Ophthalmology and Therapy. 2023.
Open the review ↗ (opens in a new tab)Background on structural and functional biomarkers relevant to AMD research.Duke startup directory: HealthLadder.AI.
View the university listing ↗ (opens in a new tab)Academic publications describe research, not commercial authorization. Authorship or institutional affiliation does not itself establish ownership of, or exclusive rights to, an algorithm or dataset.
Website information
This informational site is intended for clinicians, researchers, investors, and potential strategic partners. It does not provide patient-specific medical advice or process medical images.
The retinal visualization and workflow demonstration are conceptual illustrations. They are not medical images, a functioning diagnostic system, or evidence of a commercially deployed product.
This version contains no contact form, analytics scripts, advertising trackers, cookies, or application-level visitor storage. The hosting provider may process technical access logs. External reference links lead to websites with their own policies.
Research findings must be interpreted in their published study context. Institutional affiliations, publication references, and device names do not imply endorsement, clinical authorization, or transferable rights.
Company and clinical information should be reviewed periodically as research, partnerships, and development plans evolve.