Confidential · The Plan

Own the rails.
Sell the proof.

Everyone in this category rents the same three things: someone else's molecule, someone else's prescriber, someone else's warehouse. They compete on ad spend and they get one margin. We own the molecule, the verification, the prescriber, the warehouse, the registry and the audience. Nine divisions, one supply chain, and the only real-world outcome dataset in peptides sitting underneath all of it. That is a category position, not a company.

82
Clinicians ordering
zero marketing spend
78
Clinicians registered
and ordering
84%+
Gross margin, proven
on receipts
$1.2B
Y3 enterprise value
base-case model

Section 01

Nine divisions. Three kinds of money.

Every division earns in one of three ways. Understanding which is which is how you decide where the next dollar goes.

TYPE 1

Molecule margin

Make it for $11.76 blended all-in. Sell it for $75 wholesale. That is 84% gross margin, already proven across a 1,221-vial retatrutide run. OTC lands near $4/unit.

Divisions: Peptide Pure · LYPHWAVES · Peptide Buzz · OTC & Brands

TYPE 2

Recurring

Subscription and per-encounter revenue that compounds without new acquisition. Telemed visits, refill programs, clinic SaaS at $500/clinic/month at 90% margin.

Divisions: National Telemed · Data Capture & Platforms

TYPE 3

Infrastructure rent

The one nobody else can offer. We sell the machine, not just the product: contract lyophilization, third-party COA testing, white-label fulfillment, prescriber access. Our competitors become our customers.

Divisions: Fulfillment & 3PL · Analytical Lab · LYPHWAVES contract capacity

The strategic read: the billion-dollar telehealth companies being written about this year are Type 1 brands renting Type 3 infrastructure from someone else. The value accrues to whoever owns the rails. We are building to be the rails and run our own brand on top of them, capturing both margins.

Section 02

Why we can do this and they cannot

Two assets sit outside the commercial structure. Neither one shows up on a P&L. Together they are the entire reason this is defensible.

GOVERNANCE · 501(c)(3)

Mortensen Medical & the IRB

IRB PPRN-001-2025 · IRCM-2025-467. A prospective multi-site observational study of peptide-supported metabolic, regenerative and performance protocols, approved by the Institute of Regenerative and Cellular Medicine IRB.

Principal Investigator: Dr. Mortensen, PA-C. Co-Investigator: Dr. Sunil Kurup. Study Coordinator: Dr. Elaine Marquez Mortensen, ND.

What it actually buys us: every clinician who buys from us can enroll as a credentialed co-investigator instead of a customer. Every vial carries a batch number, a COA and an unbroken chain of custody. Every outcome is consented, captured and citable.

A competitor can copy a formula in a week. They cannot copy four years of consented longitudinal outcomes. The nonprofit holds the protocol and the data governance and sells nothing — that separation is exactly what makes the dataset worth anything.

LEGAL · THE DEFENSE

Kaveh Newmen — Regulatory & IP Counsel

The best peptide attorney in the country, and he is not learning this category on our clock. He defends AlphaBioMedLabs, Paramount Peptides and Trevor Kruder's organization daily — the largest operators in the space.

That matters more than it sounds. He has already seen the enforcement letters, the payment-processor terminations and the state board actions that are coming for everyone else. We are not writing our compliance posture from a blog post. We are writing it from the guy who handles the actual files.

Currently on: the operating agreement and GM equity benchmarks · the parent holdco formation · PMA and 503 structuring · the data-licensing entity question · the patent estate.

Mort quarterbacks. Josh runs the offense. Kaveh runs the defense. In a gray-market category, the defense is what determines whether you get to keep the points.

Section 03

Four regulatory lanes, four different speeds

We have been carrying the heaviest lane's burden across all four. Sorting the catalog is the single fastest unlock available to us — two of these lanes can turn on in weeks.

LaneWhat's in itWhat it needsTime to revenue
1 · True OTCPouches, sleep & energy strips, topicals, beverageNo prescriber. No pharmacy. No 503. Supplement/cosmetic rules and clean claims.NOW
2 · Commercial generic RxTadalafil, sildenafilFDA-approved molecules. No compounding at all. Prescriber plus an ordinary mail-order pharmacy.WEEKS
3 · Compounded non-sterile RxPT-141/tadalafil strips, combination capsules503A, patient-specific prescription, USP 795. A sanitized room, not a cleanroom.1 QUARTER
4 · Compounded sterile RxEvery injectable peptideUSP 797, sterility, endotoxin, full quality system. Runs under the IRB today.RUNNING

Section 04

What each division is worth

Year-one model targets by division. Where a number is proven on receipts it is marked. Everything else is a model output, not a promise.

#DivisionHow it earnsY1 targetMarginStatus
01Peptide Pure
Clinician channel
Wholesale to clinics under IRB$7.26M84%+Revenue today
02LYPHWAVES
Manufacturing + analytics
Own-plant margin, then contract capacity$280M
capacity at full rate
Cost center → profitEquipment en route
03National Telemed
Prescriber layer
Per-encounter + refill subscriptionUnlocks all RxRecurringStanding up
04Peptide Buzz
Premiere OTC brand
DTC and bulk to clinicians — the only brand doing both$1.8M62%Storefront live
05OTC & Brands
KULT · DRYP · LIIT · stripped
PMA membership, restricted-category DTC, retail tinsPortfolio~$4/unit costSelling
06Data Capture
The flywheel
Clinic SaaS $500/mo, then data licensing$189K90%Tool shipped
07Killer Health Studios
Demand engine
Owned audience feeding every brand$396K90%In production
08Fulfillment & 3PL
Scale & margin
White label + fulfillment as a service$168K provenPer-unitKYVO shipped
09CLASSIFIED
The moonshot
Patent pending · FDA drug developmentAsymmetricValidation to FDA

The compounding effect nobody models: the analytical lab alone runs roughly $1.2M/year per instrument at 85%+ margin on a floor we already lease, using a machine we already need. Two instruments is a $2.4M business hiding inside a cost center. That pattern repeats across every Type 3 division.

Section 05

How fast, and how much

Four phases. Each one is funded by the phase before it. The only phase that requires outside capital is the second, and it is the one that changes the shape of the company.

Phase 1
Days 0–90
$250K
Monthly run rate

Turn on what is already built

  • Lane 1 OTC live on our own rails — no prescriber, no pharmacy, no permission required. Inventory is sitting in the warehouse.
  • Lane 2 generic Rx funnel — one SKU, one page, AI-built. The fastest legitimate Rx revenue available to us.
  • LegitScript application filed day one. Three to six months of lead time. Everything downstream waits on it, so it starts before the funnel does.
  • White-label repeat orders — the KYVO program proved the model at 32,000 units.
  • Cost: essentially zero incremental. This phase is execution, not capital.
Phase 2
Months 3–9
$1M
Monthly run rate

The plant goes hot and the prescriber goes national

  • LYPHWAVES operational. COGS drops from outsourced to $10.80/vial all-in. That single change is worth more than most companies' entire gross profit.
  • National telemed live in 50 states — every Rx SKU in the group plugs into one prescriber layer built once.
  • LegitScript lands → Google and Meta healthcare advertising unlock, card networks stabilize, paid acquisition turns on.
  • Analytical lab opens as a revenue line at $215–$450 per sample.
  • This is the raise. $2M at a $20M post for 10%, or $3.5–4M to run the market-leader case. Capital buys equipment completion, inventory working capital that turns in ~6 months, and quality/regulatory leadership.
Phase 3
Year 2
$3–5M
Monthly run rate

Sell the machine

  • Infrastructure product packaged and priced — supply, COA verification, prescriber access and fulfillment sold as a white-label stack. Every competitor becomes a customer.
  • Data licensing begins. The registry is now the only real-world peptide outcomes dataset with consent, chain of custody and third-party verification behind it.
  • ~300 clinics on the model. Blended LTV:CAC of 16.6:1 with roughly a two-month payback.
  • Model output: $5.13M+ revenue, ~$1.24M operating cash at the conservative end; the market-leader case runs materially higher.
Phase 4
Year 3
$1.2B
Enterprise value

The category, not the company

  • Model: $205M revenue · $121M EBITDA → roughly $1.23B at 6× revenue, cross-checked at 10× EBITDA. Upside case ~$1.87B.
  • Published outcomes go to Congress and the agencies. Kaveh and Kaveh's network on the regulatory side, our registry on the evidence side. If the rules move, they move around the dataset we own.
  • The moonshot resolves one way or the other. Patent pending, validation protocol with the FDA, roughly one-in-three odds — which for a moonshot is very good and is not in any of the numbers above.

Section 06

What has to be true

The plan above is the upside. This is the list that decides whether we get there. Every item has an owner.

RISK 01

LegitScript timing

Three to six months solo. It gates paid acquisition and payment stability across every Rx lane. If it is not filed in week one, Phase 2 slips a quarter.

RISK 02

Single-source anything

The billion-dollar comparables in this space depend on one infrastructure vendor. Two of everything — pharmacy, 3PL, lyo, testing — from day one.

RISK 03

An unreviewed claim

One disease claim turns a supplement into an unapproved drug. The compliance review ships before the first paid ad, not after.

RISK 04

The data entity

Commercial data licensing cannot sit inside the 501(c)(3). Needs a for-profit registry entity with a license to de-identified data. Kaveh.

RISK 05

Three open GM seats

LYPHWAVES, 3PL and the data-collections owner. A division without a GM is a division that does not compound. Step up, or find yourself with a boss.

RISK 06

Regulatory reset

Compounded GLP-1 and gray-market peptides can change status. Our hedge is the same thing as our moat: the IRB, real COAs, and counsel who defends the biggest players in the category.

The one-line version

Everyone else sells the product.
We sell the product and own the proof it worked.

Then we take the proof to the agencies and move the rules the whole category operates under. That is the billion-dollar arm. The nine divisions are how we fund the walk there — profitably, from month one, on margins nobody renting their supply chain can match.

Confidential · h2bab HQ · not for distribution
Revenue figures marked "proven" are on receipts. All forward numbers are model outputs, not guarantees.
Numbers refresh every Monday from the books.