BREAKING Autem Therapeutics treats cancer with electromagnetic frequencies FDA BREAKTHROUGH DEVICE designation for advanced liver cancer $10M Series A-1 led by Zentynel Frontier Investments AutEMsys: no scalpel, no chemo, no refrigeration 66-patient feasibility study shows early signals of tumor shrinkage Built in Hanover, New Hampshire
Company Profile · Bioelectric Oncology

Autem Therapeutics

A cancer company that doesn't reach for the scalpel or the chemo drip. It reaches for a frequency.

Hanover, NH Founded 2017 ~15 people AutEMsys
Autem Therapeutics logo
EXHIBIT A: The logo of a company betting that cancer has an electrical weak spot. Filed under "things that fit in a clinic with no fridge."
Who they are now

A clinic visit, a calibrated signal, and a patient who keeps the rest of their day

Picture a treatment room with no IV pole, no warning labels about toxicity, no cold-storage unit humming in the corner. A patient sits down. A device delivers a low-level, amplitude-modulated electromagnetic signal tuned to their tumor. Then they go home. This is the room Autem Therapeutics is trying to build at scale - and the one cancer medicine has rarely offered.

Autem Therapeutics is a bioelectric oncology company headquartered in Hanover, New Hampshire - a town better known for Dartmouth than drug pipelines. Its product, AutEMsys, is a non-invasive, non-toxic system that treats solid tumors with electromagnetic frequencies rather than molecules. The lead target is hepatocellular carcinoma, the most common form of liver cancer and one of the harder cancers to treat well.

The pitch is almost suspiciously simple: don't poison the patient. Retune the tumor.

- The Autem thesis, paraphrased
The problem they saw

Cancer care that works often asks the patient to suffer for it

Surgery, chemotherapy, radiation - the standard arsenal is effective and brutal in roughly equal measure. For liver cancer, the picture is harder still: many patients are diagnosed late, tumors recur, and the treatments that exist can be as taxing as the disease. The side effects aren't a footnote. They're the reason a lot of people stop treatment.

There's a second problem, quieter but just as stubborn. Most advanced cancer therapy assumes a wealthy hospital: cold-chain logistics, infusion suites, specialist staff. That assumption quietly writes off enormous parts of the world. A drug that needs refrigeration and a sterile IV line is a drug that doesn't travel.

A therapy that needs a refrigerator is a therapy with a very short passport.

- On why access is an engineering problem, not just a moral one

Autem's founders looked at both problems and saw the same root: the tools were built to attack cancer chemically, and chemistry is heavy, toxic, and hard to ship. What if the lever was physical instead?

The founders' bet

An oncologist who got tired of the menu

The company traces back to 2017 and Frederico Costa, a medical oncologist who had spent his career inside the chemical paradigm and wanted a different lever. The bet he and the team made rests on the Warburg effect - the long-observed fact that cancer cells run an unusual, energy-hungry metabolism that sets them apart from healthy neighbors. If cancer cells are electrophysiologically out of sync, the reasoning goes, perhaps the right electromagnetic frequencies can nudge them back toward balance, or starve their abnormal rhythm.

It's a physics answer to a biology question. That's exactly why it needed an unusual team. Michael Choukas joined as co-founder and stepped in as CEO when the company raised its Series A, pairing Costa's clinical science with operating leadership.

Frederico Costa
Co-Founder & Chief Scientific Officer

Medical oncologist; originated the bioelectric approach to solid tumors and the science behind AutEMsys.

Michael Choukas
Co-Founder & CEO

Leads the company's operations, regulatory strategy, and push toward clinical trials and access.

Our team is passionate about developing a non-invasive, non-toxic, globally accessible cancer treatment.

- Michael Choukas, CEO, Autem Therapeutics
The product

AutEMsys, explained without the hand-waving

AutEMsys delivers personalized, low-level, amplitude-modulated electromagnetic frequencies to a patient's whole system, on a schedule of two- or four-week intervals. The signals are meant to be tumor-specific rather than a single generic broadcast - the device is doing calibration, not just emission.

The engineering choices say a lot about who Autem is designing for. One unit can serve up to 40 patients a month. It needs no refrigeration. That isn't a spec-sheet flourish; it's the whole accessibility thesis turned into hardware. A device that runs without a cold chain is a device that can sit in a clinic far from a major cancer center.

Non-invasive

No surgery, no implant. The therapy is delivered externally.

Non-toxic

Electromagnetic frequencies instead of cytotoxic drugs - aimed at sparing healthy tissue.

Portable

No refrigeration required, so it can reach remote and low-resource settings.

Personalized

Frequencies tuned to be tumor-specific, blending physics, AI, biology and medicine.

The technology combines physics, artificial intelligence, biology and medicine to create better cancer treatments.

- Cristian Hernandez, Zentynel Frontier Investments
Milestones

From a clinical hunch to a Breakthrough Device

2017

The bet is placed

Founded around oncologist Frederico Costa's idea that solid tumors have an electromagnetic weak spot.

Feasibility era

66 patients, early signals

Initial clinical feasibility studies in hepatocellular carcinoma suggest tumor shrinkage, better quality of life, and extended survival.

June 2022

$10M Series A-1

Led by Zentynel Frontier Investments. Michael Choukas named CEO. Funds aimed at next-gen AutEMsys, regulatory work, and a pivotal HCC trial.

FDA

Breakthrough Device designation

AutEMsys earns FDA Breakthrough Device status for advanced HCC - a fast-track lane for promising tech.

February 2024

Series A extended

An additional $1.5M raised to keep the development engine running.

2H 2025

Into the clinic

Anticipated FDA IDE approvals to begin clinical trials in liver cancer (HCC) and glioblastoma (GBM).

The proof, so far

Numbers that are promising, not yet conclusive

Early-stage device companies live in the gap between "interesting signal" and "proven therapy." Autem's published markers sit squarely in that gap - enough to earn an FDA Breakthrough nod, not yet enough to declare victory. Here's the shape of the evidence.

Feasibility patients
66 in HCC
Series A-1
$10M
Series ext.
$1.5M
Capacity / unit
40 patients / month
Bars are scaled for readability, not a single shared axis - they mix patients, dollars, and throughput on purpose. The honest caption: a small but real body of evidence, a modest war chest, and a machine designed to serve a lot of people per unit.
2Cancers in trial plans (HCC + GBM)
0Refrigerators required
~15People on the team
$11.5MDisclosed Series A capital
The mission

Make cancer treatment safe, effective, and reachable

Most mission statements pick one virtue and lean on it. Autem's stacks three that usually trade off against each other: safe, effective, accessible. The toxic treatments tend to be the powerful ones. The accessible treatments tend to be the cheap, weak ones. Autem's wager is that a physical, hardware-based therapy can refuse that trade - delivering real anti-tumor effect without the toxicity, in a form that can travel past the walls of an elite hospital.

The hard part isn't inventing a therapy. It's inventing one that a clinic in a remote area can actually run.

- The accessibility problem, stated plainly

That ambition is why the company keeps pairing its science claims with logistics claims. No refrigeration. Forty patients a month. Two- or four-week intervals. These aren't marketing lines - they're the difference between a therapy that helps a few thousand insured patients and one that could reach people the current system never planned to serve.

Why it matters tomorrow

Back to that quiet treatment room

Autem still has the hardest mile ahead: the controlled clinical trials that turn a Breakthrough designation into approved medicine. Bioelectric oncology is a young field, and skepticism is the correct default - frequencies are easy to promise and hard to prove. The IDE-gated trials in HCC and glioblastoma are where the thesis either holds or doesn't.

But return to the room from the opening. No IV pole. No toxicity warnings. No humming fridge. A patient sits, receives a tuned signal, and reclaims the rest of their day - and, if the data holds, gets that day in a clinic that could never have run a chemo suite. That room used to be a fantasy. Autem Therapeutics is trying to make it a floor plan.

Cancer care has spent a century getting more powerful. Autem is betting the next chapter is about getting more reachable.

- The closing argument