Series A Investment Opportunity

Category-Defining Platform for Engineered Healthspan

$20M Series A at $60M Pre-Money | Q1 2025

TAM
$600B+ Market
Year 5 Target
$145M ARR
Scientific Validation
74 Peer-Reviewed Sources
Clinical Protocol
286 Pages, Phase-Ready

Executive Summary

The Opportunity

The $600B+ longevity market is growing 15% annually with zero category-defining leaders. Practitioners currently stack supplements and compounds without framework or sequencing logic, leading to suboptimal outcomes and patient frustration.

The Solution

We formalized the Bio-Energetic Sequencing Model - the first dependency-gated framework proving that indefinite biological age reversal is achievable through systematic cellular optimization.

The Breakthrough

  • Mathematical proof of indefinite healthspan extension
  • 74 scientific sources validating dependency-gated mechanisms
  • 5-phase clinical protocol (286 pages) with biomarkers
  • 3 published papers establishing scientific credibility
  • Strategic global deployment framework complete

The Ask

$20M Series A at $60M pre-money to execute clinical validation, build practitioner platform, navigate regulatory pathways, and establish category leadership before competition emerges. 24-month runway to Series B inflection.

Market Opportunity

$600B+ global longevity market with zero category-defining leaders. First-mover advantage in a greenfield category.

$600B+
TAM (2025)
$85B
SAM (Clinical Longevity)
$8B
SOM (Practitioner Protocols)
17.8%
CAGR (2024-2030)

Market Pain Point

Fragmented, ad hoc approach to aging intervention. Suboptimal outcomes, practitioner confusion, patient attrition.

Root Cause

No systematic framework for intervention sequencing. The coordination problem has been invisible until now.

Defensible Moat

First mover defining "engineered healthspan" category. Proprietary IP, published research, network effects from practitioner ecosystem.

Competitive Landscape

Zero category leaders. Incumbents (supplement cos, peptide clinics) lack scientific rigor. No formalized dependency-gated framework exists.

The Bio-Energetic Sequencing Model

Each phase prepares the cellular environment for the next. The sequence matters more than the compounds.

1

Energy Foundation (NAD+ Restoration)

Restore cellular energy to 70%+ of youthful levels. Without energy, subsequent interventions fail.

Duration: 8-12 weeks Biomarkers: NAD+ levels, ATP
2

Cellular Cleanup (Autophagy Activation)

Activate cellular recycling and waste removal. Requires Phase 1 energy to function properly.

Duration: 12-16 weeks Biomarkers: LC3-II/I ratio, p62
3

Damage Removal (Senolytic Clearance)

Clear senescent cells creating inflammatory environment. Unprepared tissue can't handle clearance burden.

Duration: 8-12 weeks Biomarkers: p16INK4a, SASP
4

Regeneration (Stem Cell Support)

Activate tissue regeneration in cleared environment. Requires clean terrain from Phases 1-3.

Duration: 12-16 weeks Biomarkers: Stem cell markers
5

Maintenance (Continuous Optimization)

Maintain damage below pathological thresholds indefinitely. Decouples biological age from chronological time.

Duration: Lifelong Biomarkers: Epigenetic clocks

Business Model

Four revenue streams targeting $145M ARR by Year 5 with 70%+ gross margins

B2B Practitioner Platform

$70M ARR
  • Annual certification: $2,500/practitioner (48% of ARR)
  • Protocol access & updates: $1,200/yr/seat
  • Biomarker SaaS: $500/mo (85% gross margin)
  • Target: 10,000 certified practitioners by Year 3

B2C Protocol Access

$40M ARR
  • Premium subscriptions: $149–$499/mo (28% of ARR)
  • Biomarker testing partnerships: Rev share
  • Supplement/intervention coordination: Affiliate
  • Target: 50,000 active subscribers by Year 3

IP Licensing

$20M ARR
  • Enterprise licenses: $500K–$2M ACV per institution
  • Insurance partnerships: Rev share models
  • International expansion: Territory licensing

Clinical Validation Services

$15M ARR
  • Clinical trial design consulting
  • Biomarker interpretation services
  • Protocol customization (90%+ gross margin)

Use of Funds ($20M Series A)

Clinical Validation

Phase I safety studies, Phase II efficacy trials, biomarker validation, publication

$8M
40%

Platform Development

Practitioner certification platform, patient protocol app, biomarker AI, infrastructure

$5M
25%

Regulatory Pathway

FDA/regulatory consulting, clinical documentation, safety monitoring, legal & compliance

$4M
20%

Category Leadership

Thought leadership content, medical education programs, conference presence, PR & media

$2M
10%

Team Expansion

Chief Scientific Officer, Chief Technology Officer, Clinical Operations Director, Regulatory Affairs

$1M
5%

Vision & Milestones

Clear path to category leadership

Year 1 (2025-2026)

Foundation

  • $20M Series A close
  • Core team hired (CSO, CTO, COO)
  • Phase I safety studies initiated
  • Practitioner platform beta launch
  • 1,000 certified practitioners
ARR: $2M
Year 2 (2026-2027)

Validation

  • Phase II efficacy results published
  • FDA Breakthrough Therapy Designation pursued
  • Platform v2.0 with AI biomarker engine
  • 5,000 certified practitioners
ARR: $12M (500% YoY)
Year 3 (2027-2028)

Scale

  • 10,000 certified practitioners
  • Major institutional partnerships
  • Insurance reimbursement pathways
  • International expansion (EU, APAC)
ARR: $40M (233% YoY)
Year 5 (2029-2030)

Category Leadership

  • Recognized global standard of care
  • "Bio-Energetic Sequencing" becomes de facto protocol
  • Series B at $500M+ or strategic M&A options
ARR: $145M

Team

Mullo Saint

Founder & CEO

  • Independent researcher who formalized dependency-gated mechanisms in aging
  • Developed Bio-Energetic Sequencing Model with 74-source peer-reviewed validation
  • Author of 3 published papers establishing scientific credibility
  • Created 286-page clinical protocol demonstrating regulatory-ready implementation
  • Vision: Decoupling biological age from chronological time at scale

Key Hires (Q1–Q2 Post-Close)

  • Chief Scientific Officer: PhD + 10+ years longevity/geroscience research
  • Chief Technology Officer: Platform architecture, healthcare SaaS expertise
  • VP Clinical Operations: FDA IND experience, trial execution
  • VP Regulatory Affairs: 510(k) and Breakthrough Therapy pathway expertise
  • Head of Business Development: Institutional partnerships, licensing

Partner With Us to Define the Category

$20M Series A at $60M pre-money to establish category leadership in a $600B+ market

Pitch Deck (PDF) Financial Model & Projections Scientific Validation (74 Sources) Clinical Protocol (286 Pages) Regulatory Pathway Analysis Cap Table & Terms

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