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JK07 Phase 2 topline readout expected first half of 2026 Salubris Bio raises $35M for Phase II Only clinical-stage selective ErbB4 agonist in development Penn virologist now runs the company Heart failure with no current treatment is the target JK07 Phase 2 topline readout expected first half of 2026 Salubris Bio raises $35M for Phase II Only clinical-stage selective ErbB4 agonist in development Penn virologist now runs the company Heart failure with no current treatment is the target
Co-Founder · CEO · Salubris Biotherapeutics

Samuel Murphy

His son tells people his dad is a drug dealer. The honest version: he is trying to repair the human heart with a molecule no one has used this way before.

Gaithersburg, MD Samuel Murphy, CEO of Salubris Biotherapeutics

The face of a forty-person company chasing a first-in-class heart drug.

2017
Co-founded Salubris
$35M
Raised for Phase II
~40
Employees
2
Clinical programs

A drug company runs on someone who can speak to a scientist and a banker in the same breath.

Samuel Murphy starts the day at 5am, five mornings a week, with a phone pressed to his ear and Shenzhen on the other end. He runs Salubris Biotherapeutics out of Gaithersburg, Maryland - a clinical-stage biotech of roughly forty people - and moonlights as the international business development head for its parent company in China. The nightly calls are not a complaint. They are the price of moving a drug across two regulatory systems at once.

The drug is JK07. It is the first and only clinical-stage selective ErbB4 agonist, and Murphy is betting it can become the first disease-modifying biologic for heart failure.

That is a strange sentence, so it is worth slowing down. ErbB4 is a receptor most cardiologists never think about and most oncologists know too well - it lives in the world of cancer signaling. Murphy's company took that biology and pointed it at the failing heart, a place with millions of patients and, for some forms of the disease, no approved therapy at all. Heart failure with preserved ejection fraction has stubbornly resisted treatment. JK07 is aimed straight at it.

From the bench to the deal table and back

Murphy did not arrive at the corner office by the usual route. He earned a Ph.D. in virology at the University of Pennsylvania, then did a postdoc in gene therapy and translational medicine at Children's Hospital of Philadelphia - in the lab of Kathy High, the work that would later spin out as Spark Therapeutics. He had every credential to spend a career at the bench.

Instead he left it. For more than a decade he sold science rather than made it: a director at PriceSpective, a senior principal at IMS Health (now IQVIA) including a stretch running consulting in China, then managing director of IMS Health Capital doing life-sciences investment banking. He learned how money looks at a molecule. Then, in 2017, he co-founded Salubris Biotherapeutics and walked back into the lab he had left - this time as the person deciding which diseases to chase. He took the CEO title in November 2020.

You should go pick a disease and cure it. His Ph.D. advisor's parting advice - which he took literally

The advice stuck. Ask Murphy what he does and the answer strips away the jargon: "I develop new medicines to treat people and cure people." His children translate it their own way. His daughter says Dad makes medicines. His son, less diplomatically, says his father is a drug dealer. Both are closer to the truth than most elevator pitches.

The bridge between two continents

Salubris Biotherapeutics is the American arm of Shenzhen Salubris Pharmaceuticals, a publicly traded Chinese drugmaker. That makes Murphy a translator in more than one sense - shuttling between a US scientific culture and a Chinese corporate one, between FDA timelines and a parent company's expectations. He describes his management style as flexible: firm when needed, soft when needed. Running a company that never fully sleeps tends to teach that.

He carries the load outside Salubris too, sitting on four company boards and chairing the board of GO Therapeutics. The throughline is the same one his advisor handed him: find the disease, build the thing that fixes it, get it to people.

The Arc

Twenty years from the lab bench to the readout that matters.

2004

Finishes a Ph.D. in virology at Penn, then a gene-therapy postdoc at Children's Hospital of Philadelphia in the lab that becomes Spark Therapeutics.

2011

Joins PriceSpective as a director, stepping from science into pharma commercial strategy.

2012

Becomes senior principal at IMS Consulting Group, later IQVIA - including a turn as head of consulting in China.

2014

Named managing director of IMS Health Capital, doing investment banking for life-sciences companies.

2017

Co-founds Salubris Biotherapeutics and joins as chief business officer.

2020

Takes over as chief executive officer in November.

2024

Salubris raises $35M to push its lead programs into Phase II.

2025

Reports positive interim Phase 2 data for JK07, completes the HFrEF cohort, and opens a pulmonary-hypertension study.

2026

The topline readout the whole company is waiting on is due in the first half of the year.

A career split almost evenly between making science and selling it.

Lab & academic training~7 yrs
Consulting & banking~6 yrs
Building Salubris2017 → now

Approximate, illustrative spans drawn from public career records.

Boards & roles he carries at once.

01 / CHAIR

GO Therapeutics

Board chair.

02 / OBSERVER

Mercator MedSystems

Board observer.

03 / CEO

Salubris Biotherapeutics

Co-founder and chief executive.

04 / BD HEAD

Shenzhen Salubris

International business development.

In His Words

Three lines that explain the whole career.

You should go pick a disease and cure it.
I develop new medicines to treat people and cure people.
My management style is flexible - firm when needed, soft when needed.

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