BREAKING  Jessicca Rege named CEO of Sus Clinicals, effective Aug 1, 2024 • The Oncopig is FDA-cleared and ready for pharma • From a Mural Oncology IPO to an 18-person startup • "My passion is to accelerate transformative research into the clinic" • A PhD in pharmacogenomics meets a pig named Sus scrofa BREAKING  Jessicca Rege named CEO of Sus Clinicals, effective Aug 1, 2024 • The Oncopig is FDA-cleared and ready for pharma • From a Mural Oncology IPO to an 18-person startup • "My passion is to accelerate transformative research into the clinic" • A PhD in pharmacogenomics meets a pig named Sus scrofa
Profile / Translational Oncology

Jessicca Rege

She took a cancer company public. Then she walked away from the ticker symbol to run a startup built around a genetically engineered pig.

CEO, Sus Clinicals Ph.D., Pharmacogenomics 15+ yrs in oncology R&D
Jessicca Rege, CEO of Sus Clinicals
The boardroom regular who bet on the barnyard. Jessicca Rege, Waltham, MA.
The Lede

A pig may know what the mouse never could

For two decades, the standard tool for testing a cancer drug before it reaches a human has been a mouse. Small, cheap, and convenient. Also, frequently, wrong. Drugs that shrink tumors in mice routinely fail in people, and the gap between the two has cost the industry billions and patients their time. Jessicca Rege runs a company that thinks the answer has been on a farm the whole time.

Rege is the Chief Executive Officer of Sus Clinicals, an early-stage biotech whose flagship product is the Oncopig Cancer Model - an FDA-cleared platform that grows human-like tumors inside genetically engineered pigs. A pig's size, physiology, and metabolism sit far closer to a human's than a mouse's does. That is the bet. And Rege, a pharmaceutical scientist with a doctorate in pharmacogenomics, is the one selling it to pharma.

She started the job on August 1, 2024, picked by the board after what its executive chair Jeffrey Weedman called "an exhaustive search." The choice carried a certain symmetry. Rege had spent her career on the human side of the equation - designing trials, building clinical strategy, raising money, taking a company public. Now she would spend it trying to make the preclinical side honest enough that fewer of those human trials end in heartbreak.

"My passion is to accelerate transformative research and therapeutics into the clinic, with the hope to save lives."

- Jessicca Rege, on taking the CEO role
The Arc

Roche to Lilly to a ticker symbol

Rege did not arrive at Sus Clinicals as a first-time operator. She arrived with a resume that reads like a tour of oncology's biggest names. Early clinical research roles at Hoffman-LaRoche and Bristol Myers Squibb. Global medical affairs leadership at Eisai. Clinical collaborations at Eli Lilly. Chief of staff for the cancer enterprise at Daiichi-Sankyo. Each stop added a different muscle: the science, the strategy, the politics of moving a molecule through a global organization.

Then she went smaller, and the stakes got personal. At OncXerna Therapeutics she served as global chief development officer, helping build the company's infrastructure from the studs and raising a $16 million Series A and an $80 million Series B. At Alkermes, which she joined in 2020 as VP and head of clinical development for oncology, she built the immuno-oncology development strategy and ran its global trials. That oncology effort spun out into Mural Oncology, where Rege became chief development officer and helped lead the company through its public offering - taking a science project and turning it into a publicly traded company.

Most executives would have planted a flag there. Rege traded it for a startup with eighteen people and a pig.

15+
Years in oncology R&D
$96M
Raised across two OncXerna rounds
8
Major pharma / biotech orgs
1
IPO helped lead at Mural
The Education

Softball scholar to pharmacogenomics PhD

Before the boardrooms, there was a softball diamond. Rege earned her bachelor's in biology at Carson-Newman College, where she was both a competitive softball player and a scholar - the kind of person who could read a curveball and a chromosome. She went on to Virginia Commonwealth University for a master's in physiology, then a doctorate in pharmaceutical sciences at the Medical College of Virginia, specializing in pharmacogenomics: the study of how a person's genes shape their response to a drug.

It is a fitting specialty for someone who would end up running a precision-medicine platform. Pharmacogenomics is the science of why one patient thrives on a drug and another does not. The Oncopig, with its CRISPR-edited, patient-tailored tumors, is that question asked at the scale of a whole animal.

EARLY CAREER
Clinical research at Hoffman-LaRoche and Bristol Myers Squibb
MID CAREER
Head of Global Medical Affairs, Oncology at Eisai; Global Clinical Collaborations at Eli Lilly
MID CAREER
Global Chief of Staff, Cancer Enterprise at Daiichi-Sankyo
MID CAREER
Global CDO at OncXerna - raised $16M Series A and $80M Series B
2020
VP, Head of Clinical Development, Oncology at Alkermes
2023
Chief Development Officer at Mural Oncology; helped lead the IPO
2024
Appointed CEO of Sus Clinicals, effective August 1
In Her Words

The patient stays at the center

Across interviews, one theme recurs in Rege's language with unusual consistency. Not the technology. Not the valuation. The patient. She talks about drug development the way someone talks about a promise they intend to keep.

"The focus still remains on our patients, and how to develop drugs that meet their unmet needs."

"As an industry, we are blessed with abilities to really make a change in the lives of patients and their families."

"Better combination strategies that are not just additive but are synergistic when used together."

"Design trials that meet patients' real-world needs and address their challenges."

The Leap

Scientist, mom, startup leader

When Rege sat down with the She Leads Biotech podcast in April 2025, she described herself with three words that rarely share a sentence: scientist, mom, startup leader. The conversation was about the unconventional path from big pharma to biotech - the move from a place with structure and budgets and a hundred colleagues to a place where the org chart fits on an index card and the science has to earn its keep every single day.

Her answer to how she navigates it is disarmingly low-tech. Authenticity and curiosity, she says, are her most powerful tools. Not a particular framework or a hard-charging operating playbook - the willingness to be herself and to keep asking questions. For a leader running a company whose entire premise is that the conventional model is incomplete, curiosity is not a personality quirk. It is the job description.

What, exactly, is an Oncopig?

// The product Rege is selling to pharma

The Oncopig Cancer Model is a genetically engineered pig that can be prompted to grow tumors resembling human cancers. Because a pig's size and physiology mirror a human's far better than a mouse's, the data it produces aims to predict - more honestly - which drugs, diagnostics, and devices will actually work in people.

1

Engineered

Pigs carry Cre-inducible KRAS G12D and TP53 R167H mutations, the genetic switches behind many human cancers.

2

Induced

Tumors are triggered in a targeted spot, and CRISPR gene editing tailors them to specific cancer types.

3

Tested

Drugs, devices, and diagnostics are evaluated in a body that behaves much more like a patient's.

4

Predicted

The result is more predictive preclinical data - and fewer expensive surprises in human trials.

Why It Matters

Closing the gap that mice can't

The translational gap - the chasm between what works in a lab animal and what works in a person - is the quiet tax on every cancer drug. Sus Clinicals holds an exclusive global license to the underlying intellectual property out of the University of Illinois, and Rege's job is to turn a clever academic model into a product pharmaceutical companies will pay for and trust.

That is the bet she left the public markets to make. Not because the Oncopig is a sure thing - no preclinical model is - but because she has watched, from the inside of eight different organizations, how often the old model lies. If a pig can tell the truth a little sooner, a few more drugs reach the patients she keeps talking about. That, in the end, is the whole pitch. And she means it.

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The Rolodex

Where to find her work

Sources: Sus Clinicals press releases, She Leads Biotech, Proventa International, Disease Models & Mechanisms. Profile facts verified from public sources.