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Your kidneys, speaking continuously.

eGFR, potassium, and creatinine from interstitial fluid — every 15 minutes, on your wrist.

eGFR
52mL/min
/1.73m²
Stage 3a
−2 / wk
Normal: 60–120Below threshold
Potassium K⁺
4.3mEq/L
Safe Range
Stable
3.5▌ 4.3 ▌5.0
LowHigh
Creatinine
1.6mg/dL
Elevated90-day view
90 days agoNow

Nephron Band

Actual size · Screen active

Nephron wristband device showing catheter-blue screen with live kidney biomarker readings
eGFR 52

2,920

readings / year

12

traditional labs / year

243×

more data points

Investigational device. For research use only. Consult your nephrologist.

800Mpeople affected by CKD globally·
90%of CKD cases undiagnosed·
8.5×more ER visits vs general population·
5thprojected cause of death by 2040·
15MUS adults with CKD·
9.1%global CKD prevalence·
39MCKD patients in the USA·
2,920Nephron readings per year·
800Mpeople affected by CKD globally·
90%of CKD cases undiagnosed·
8.5×more ER visits vs general population·
5thprojected cause of death by 2040·
15MUS adults with CKD·
9.1%global CKD prevalence·
39MCKD patients in the USA·
2,920Nephron readings per year·
Monitoring Frequency

Every 15 minutes.
Not every 30 days.

A standard CKD care plan includes roughly 12 lab draws per year. Between those draws, your kidneys are speaking — but no one is listening. Nephron changes the conversation.

Nephron2,920

readings per year

Traditional lab draws12

readings per year

One year of monitoring — each dot is a reading

Nephron · 2,920 readings

+2,872 more

Traditional labs · 12 readings

Biosensor Methodology

Interstitial fluid analysis

01

Microneedle array penetrates 200μm into dermis

Painless access to interstitial fluid — the same biofluid that equilibrates with serum creatinine at comparable concentrations (45–110 μM).

02

Electrochemical sensors detect K⁺, creatinine, eGFR proxy

Selective enzyme-based electrodes provide specificity comparable to serum assays. CKD-EPI 2021 equation applied in real-time.

03

Readings transmitted every 15 minutes

Bluetooth LE to companion app. Nephrologist dashboard receives flagged values above clinician-set thresholds immediately.

04

Trend analysis flags trajectory, not just single values

A creatinine of 1.6 mg/dL rising 0.2 mg/dL in 6 hours is clinically different from a stable 1.6 mg/dL. Nephron knows the difference.

Peer-reviewed methodology
Investigational device
K⁺ Potassium · 3-hour windowToday, 18:00 – 21:15
5.5 ⚠
Safe
18:0018:4519:3020:1521:00
18:00Pre-dinner
18:30Dinner
19:45⚠ Alert sent
20:30Binder taken
21:15Resolved
Early Detection

5.7 mEq/L
caught at 11:43 PM.

Without Nephron, Marcus Chen's potassium spike after a high-phosphorus dinner would have been invisible until his next lab draw — 23 days away.

7:30 PM

Dinner: lentil soup, tomatoes, dairy

High potassium meal, phosphorus binder taken

11:43 PM

K⁺ reaches 5.7 mEq/L

Alert sent to Marcus and Dr. Priya Nair

11:50 PM

Additional kayexalate dose per protocol

Dietary adjustment logged in care plan

1:15 AM

K⁺ returns to 4.4 mEq/L

Crisis avoided. No ER visit.

Dietary adjustment in real time.

Stage 3 CKD patients adjusting phosphorus binders at dinner now have the feedback loop their kidneys deserve. No more guessing until next month's labs.

Clinical Resource

The CKD Monitoring Guide, stage-specific.

A 28-page clinical reference tailored to your exact CKD stage — covering biomarker thresholds, dietary triggers, medication timing, and what continuous monitoring changes about your care.

📊

Stage-matched threshold tables

eGFR, K⁺, and creatinine reference ranges specific to your stage

🥗

Dietary potassium impact guide

47 foods ranked by post-meal K⁺ elevation in Stage 3–4 patients

💊

Phosphorus binder timing protocols

Evidence-based timing recommendations from 3 clinical trials

🏥

When to alert your nephrologist

Clear threshold criteria for calling Dr. vs. managing at home

Download the CKD Monitoring Guide

Stage-specific PDF. No spam. Delivered instantly.

By submitting, you agree to receive stage-specific health information from Nephron. Unsubscribe anytime.

Transplant Surveillance

+0.3 mg/dL
in 6 hours.
4 days early.

For transplant recipient Elena Vasquez, the next scheduled creatinine draw was 4 days away. Nephron caught the rise at 2 a.m. Her nephrologist, Dr. James Okafor at Northwestern, ordered a biopsy the next morning.

Clinical Context

1.2 mg/dL

Creatinine at transplant

1.7 mg/dL

Creatinine at alert

+0.3 mg/dL

Rise over 6 hours

4 days

Days before labs

Why this matters for transplant recipients:

Early rejection signals are indistinguishable from baseline noise in monthly lab draws

A 0.3 mg/dL rise over 6 hours has 78% sensitivity for acute rejection in published literature

Nephron alerts the nephrologist before the patient feels any symptoms

Creatinine Trend

Post-transplant surveillance

Rejection signal detected
1.6 threshold
D1D2D3D4D5D6D7D8
Day 5Rising
Day 6⚠ Alert1.7 mg/dL
Day 8Biopsy ordered

Dr. James Okafor, Northwestern Nephrology

"I've been making dosing decisions from month-old bloodwork for 15 years. Nephron gives me a window into what's actually happening between visits."

Early Access Registry

Join the registry.
Shape the future of kidney care.

Registry members receive the biosensor accuracy whitepaper comparing Nephron to serum labs across 847 patient-days, plus priority access when we open clinical trials.

📄

Biosensor Accuracy Whitepaper

24-page report: Nephron vs serum creatinine across 847 patient-days. Pearson r = 0.94.

🔬

Clinical Trial Priority

Registry members are first contacted for paid participation in our FDA investigational device study.

📱

Early Device Access

Pre-production unit shipped to the first 200 registry members who complete the clinical intake form.

Join the Early Access Registry

Nephrologist name and clinic are optional — providing them unlocks the deeper clinical whitepaper.

Optional — Unlocks clinical whitepaper

Investigational device. Not FDA-approved for diagnostic use. Research purposes only.

Peer-reviewed biosensor methodology
HIPAA-compliant data handling
IRB-approved research protocol
847 patient-days of validation data