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Emily Fox, Ava Kosinski, Chloe Mobley, Emma Niszczak, Amy Rodriguez, and Ted Sherman

ES395

epimonitor

epilepsy monitor

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Emily Fox

Psychology Major

Business Minor

epimonitor team

Ava Kosinski

Business and

Design Dual Major

Chloe Mobley

Communications Major

Business Minor

Emma Niszczak

Microbiology Major

Business Minor

Amy Rodriguez

Design/Anthropology

Business Minor

Ted Sherman

Political Science Major

Business Minor

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Real-time drug monitoring for epilepsy patients using a wearable biosensor device

Continuously measures anticonvulsant medications in the bloodstream and alerts patients before levels drop too low

Personalized sensing technology calibrated to specific seizure medications like Keppra or Lamictal

What We Do

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Bridges the gap between dosing and breakthrough seizures by providing data that traditional lab tests can’t offer

Company Description

Empowers patients and clinicians with accurate, on-demand insights to improve medication adherence and outcomes

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Product Description

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Product Features

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01

We provide a dedicated profile section to help you manage your epilepsy, track changes in your health, and monitor important blood levels for better care.

HEALTH METRICS

02

Stay on top of your treatment with our medication reminders. Set personalized alerts to ensure you take your anti-epileptic medications on time.

MEDICATION REMINDERS

03

Access reliable, easy to read resources in our Education Hub. Learn about epilepsy, treatment options, lifestyle tips, and ways to live.

EDUCATION HUB

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Product/Service Design

Accessibility and functionality is our priority. Epimonitor keeps you connected on mobile, desktop, and wearable devices.

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Wearable Technology

Desktop Mode

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Market Analysis

  • Projected growth for epilepsy monitoring devices
  • The Americas hold 45.21% of the market, Europe & Australia holds 30.88% and Asia holds 23.92%
  • 3,538,638 active cases of epilepsy in the U.S. in 2021
    • 11.5% of cases are children
    • 90% of epileptic patients take seizure medication

2021

$482.9 M

2027

$637.8 M

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Competition

  • Empatica
    • only FDA-approved seizure monitoring device
  • Epilert
    • wearable for seizure monitoring
  • Lifelines Neuro Co.
    • at-home epilepsy diagnosis
  • Emotiv
    • at-home EEG for seizure monitoring
  • Smart Monitor
    • detects and alerts possible seizures using existing Apple Watch technology

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S

W

T

W

O

  • Novel monitoring technology
  • High impact, necessary product

  • Government regulations
    • FDA
  • Existing patents
  • Extended time for product development

  • Expand technology to monitor levels of other drugs

  • Existing wearable devices for seizure monitoring
  • New epilepsy treatments

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TikTok

Instagram

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Income

Promotional

Demand

Age

**

$

1

13-22

***

$$

Instagram

Youtube

2

23-35

****

$$$

Email

Doctor Referral

3

36-55

****

$$$$

Healthcare providers

Clinics

4

56+

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Price

$600

$700

$800

$800

Marketing Strategy

Consumer Segmentation

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Target Market

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    • Manage epilepsy independently
    • Prioritize health and safety
    • High income, purchasing power
    • Trust in medical professionals

Adults aged 36-55

Peace of mind, independence, and confidence in managing their condition

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Operations

  • The business will be based in Boston, Massachusetts
    • Access to leading medical institutions, research universities, and talent
    • Proximity to many FDA consultants and testing facilities
  • The Boston facility will serve as a central hub for operations, research, and quality control
  • Our product distribution process will use a hybrid model that includes both B2B and B2C aspects
    • Direct sales to hospitals and clinics
    • Partnerships with medical device distributors
    • Direct to consumer

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Financials

Snapshot & Investor Returns

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Years After Launch

Revenue

EBITDA

Year 1

$3 M

($4 M)

Year 2

$12 M

($1 M)

Year 3

$35 M

$10 M

Break-even: Year 3 after FDA clearance

Profitability: Year 3 onward

Investor Exit: Target Year 7, at 4–6× revenue (based on CGM / digital neurology comps)

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Funding

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Total Capital Required: ~$18–22M Pre-Commercialization

Targeting:

Healthcare-focused VC

Health & MedTech angel investors

University-affiliated research funds

Grants (NSF, NIH)

Seed Round: $3–4M

Series A: $7-9M

Series B: $8-9M

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Risks

R&D complexity

Manufacturing Scalability

FDA

Requirements

User

Adoption

Data

Privacy

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Clinical Validation

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Timeline

2030

Clinical Trials & Regulatory Preparation

  • Validate device accuracy against standard blood tests across daily living conditions
  • Finalize hardware, algorithm calibration, and safety data
  • Prepare and submit FDA regulatory pathway package

2032

Market Launch & Scaling

  • Launch first commercial model supporting the top anticonvulsant medications
  • Partner with neurologists, clinics, and hospitals for distributions
  • Scale manufacturing, explore insurance reimbursement, and expand globally

2026

Concept Validation & Feasibility

  • Establish scientific feasibility of real-time anticonvulsant detection using biosensors
  • Build initial benchtop prototypes and conduct in-vitro tests with simulated plasma

2028

Prototype Development & Preclinical Testing

  • Create the first wearable prototype integrating the biosensor
  • Build early software and alert system
  • Conduct lab performance testing and early preclinical validation
  • File patents and begin FDA pre-submission consultations

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Thank You!

Questions?

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