Skip to main content
Clinical Decision Support

Kidney risk is hiding in data you already collect. NephroSense AI reads it.

Routine blood panels carry a kidney-risk signal the creatinine threshold cannot see. One platform surfaces it, for the clinic and for research.

Review queueIllustrative — synthetic data
Pt 04831routine visit
unremarkable · no flag raised
Pt 11274routine visit
unremarkable · no flag raised
Pt 02956routine visit
unremarkable · no flag raised
Pt 19408routine visit
unremarkable · no flag raisedPrioritize — confirmatory kidney evaluation
→ eGFR + urine albumin (uACR)
Pt 07362routine visit
unremarkable · no flag raisedPrioritize — confirmatory kidney evaluation
→ eGFR + urine albumin (uACR)
Pt 23517routine visit
unremarkable · no flag raised

Routine records. Nothing flagged.

Evidence
Retrospective feasibility demonstrated on a US adult clinical cohort. Independent external validation is in progress and is not yet complete.
IP
Patent-pending technology. Provisional patent filed March 2026.

Award · Peer-Review Presentations: Innovation Track

First place, Innovation Track

DCI Network AI Conference 2026 · Harvard Medical School, Boston ·

Winning paper
“Directing the Test That Was Never Ordered: Pre-Specified Temporal Evaluation of a Case-Finding Model for Albuminuria in Adults With Preserved eGFR”

Presented by Poornima Dubey, PhD, Co-Founder and Chief Executive Officer · one of three papers selected through double-blind peer review

Awarded atDCI Network AI Conference 2026Beth Israel Deaconess Medical Center, Harvard Medical School Teaching Hospital
Read the story →

One Platform, Two Channels

One platform foundation. Separate models, workflows, and evidence paths.

Biopharma Research · near-term focus

STRATA

Open for sponsor collaboration

Cohort construction for kidney and cardio-renal programs

Estimate the candidate population a site actually holds before you select it, rather than after.

For Clinical operations · Feasibility · Clinical development · Medical affairs

Explore the research platform4 further programs, each carrying its stage

Health Systems · clinical foundation

VANTAGE

Available today

CKD risk triage from the panel you already drew

Risk triage at the point of care.

For Clinicians, primary care groups, FQHCs

How It Works

From the panel on file to a clinical next step.

US adults with CKD
37M
of them don't know they have it
87%

Sources

  1. 01

    Use the panel already on file

    Enter values or upload a lab report. No new tests, no new hardware.

  2. 02

    Get a risk score in under ten seconds

    With a confidence signal alongside, so the strength of the result is visible before you act.

  3. 03

    Act on KDIGO-aligned next steps

    Confirmatory testing and referral guidance, as a PDF or FHIR R4 summary, under physician review.

nephrosenseai.com

Clinical Considerations

High

Nephrology Referral

High-risk CDS flag plus abnormal routine labs warrant expedited physician review

Moderate

Blood Pressure Optimization

Target < 130/80 mmHg per KDIGO guidelines

Routine

Lifestyle Modifications

Dietary sodium restriction and regular physical activity

Illustrative — synthetic data. Not a real patient or a performance claim.

See the walkthrough →

Latest

Where we've been lately

Team

Built by scientists, physicians and AI engineers

Dr. Poornima Dubey, PhD

Dr. Poornima Dubey, PhD

Co-Founder, Chief Executive Officer

MIT · HMS · IIT · AI/ML · Nanobiotech · HealthTech

Dew Prabhakar, MBA

Dew Prabhakar, MBA

Co-Founder, Chief Marketing Officer

IIM · Ops · Strategy

Dr. Nisha, MBBS

Dr. Nisha, MBBS

Co-Founder, Chief Clinical Officer

KGMU · Clinical Oversight

AJ

Dr. Amit Jain

Co-Founder, Chief Technology Officer

CS/AI Engineer

Institutional Ties & Background

Harvard Medical SchoolMassachusetts Institute of TechnologyIIT RoorkeeIIM RanchiKing George's Medical University, LucknowNSF I-CorpsPenn StateUniversity of Maryland, BaltimoreUniversity of CincinnatiUCL School of PharmacyBacked byC10 Labs accelerator

Physician oversight required. NephroSense AI does not provide diagnoses and has not yet received FDA classification or clearance.

Advised by clinical, commercial and regulatory veterans. Meet the advisory board →

Ready to see what your routine data holds?

Start a conversation about a retrospective look-back, or try the clinical demo with built-in scenarios.