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Neobe Therapeutics: Genetically-Engineered, ECM-Degrading Bacteria for Solid Tumors

Neobe Therapeutics

Neobe is a UK-based biotech engineering tumor-targeting bacterial therapies to dismantle fibrotic barriers in solid tumors. 

Neobe’s Story: Featuring CEO & Co-Founder Pedro Correa de Sampaio, PhD

B2B Brief: Neobe Therapeutics

Neobe Therapeutics is a UK-based biotech developing engineered bacterial therapies designed to break down fibrotic barriers in solid tumors. By targeting the tumor microenvironment – not the tumor cells directly – Neobe enables more effective penetration of immune cells, biologic therapies, and even things like chemotherapy, potentially transforming outcomes in traditionally refractory cancers.

Founded by cancer biologist Pedro Correa de Sampaio, PhD (PhD from Cambridge, post-doc MD Anderson) and bacterial engineer Annelise Soulier, Neobe was launched through Deep Science Ventures and brings together multidisciplinary expertise in tumor biology, microbial engineering, and synthetic biology.

Neobe’s platform uses commensal-derived, live bacteria engineered with biosensors that detect tumor-specific environmental cues (such as hypoxia, low pH, and nutrient profiles). Once inside the tumor, these bacteria locally secrete ECM-degrading enzymes (e.g., hyaluronidase), “softening” the tumor and improving perfusion, immune infiltration, and ultimately therapeutic efficacy.

Preclinical studies in triple-negative breast cancer and pancreatic cancer models show complete responses in tumors previously resistant to checkpoint inhibitors. The company aims to enter clinical trials in 2027, positioning its platform as a tumor-priming modality for use alongside immune checkpoint inhibitors, CAR-T cells, ADCs, and other therapies.

Due Diligence

This is new: 

Neobe is tackling a long-overlooked problem in oncology: immune and drug exclusion due to dense, fibrotic tumor stroma. Their platform is differentiated by its non-immunogenic, extracellular, and programmable design, offering broad compatibility with existing cancer therapeutics. 

This is different:

Unlike other microbial immunotherapy companies focused on immune activation, Neobe is remodeling the tumor microenvironment to remove physical barriers and boost response rates across multiple drug classes

Biological Uncertainty

Neobe’s microbes rely on sensing specific intratumoral cues – like hypoxia, acidity, and metabolite shifts – to activate ECM-degrading enzyme release. While these conditions are commonly associated with dense fibrotic tumors, they aren’t universally present.

That raises a key question:
Could some tumors have a thick ECM but lack the microenvironmental “activation signals” required to trigger Neobe’s payload? If so, efficacy could vary tumor-to-tumor, potentially limiting the platform’s reliability in certain settings.

Regulatory Hurdles:

As a live bacterial gene therapy, Neobe faces regulatory and safety complexities. Although the platform uses commensal strains and includes safety controls (e.g., non-pathogenic chassis, plasmid stabilization, antibiotic sensitivity), clinical validation of biodistribution, persistence, and redosing feasibility remains a key inflection point.

Unorthodox Manufacturing:

Manufacturing coordination between microbial production and sterile fill-finish also presents operational hurdles – the “sterile fill-finish” folks tend to not like bacteria…you see the problem.

Others exist:

Several companies like Salspera, Actym, and T3 Pharma are developing other bacteria-based cancer therapeutics. Most use attenuated pathogens to deliver immune-stimulating payloads into tumors.

But Neobe is different:

In contrast, Neobe uses commensal-derived bacteria to remodel the extracellular matrix, improving drug and immune cell infiltration. Rather than activating the immune system directly, Neobe acts as a tumor-priming platform, enabling other therapies to work more effectively by breaking down physical barriers within the tumor microenvironment.

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Neobe Therapeutics

Founded:

2021

Location:

London, England

Stage:

IND-Enabling

Status:

Private

Funding to date:

$2.3M

Share profile:

Key Leadership

Pedro Correa de Sampaio, PhD

CEO & Co-Founder

Annelise Soulier, PhD

CSO & Co-Founder

Keith Blundy, PhD

Director & Chairperson

Notable Investors

Meet the Hosts

Jeff Martin, PhD

Co-Founder Bio2Bedside

Ben McLeod

Co-Founder Bio2Bedside

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Neobe Therapeutics: An Introduction

What is Neobe Therapeutics and how did it get started?

Pedro Correia de Sampaio is the co-founder and CEO of Neobe Therapeutics, a UK-based biotech tackling fibrotic barriers in solid tumors that block immune cells and drugs from reaching cancer cells.

With a PhD from Cambridge and a postdoc at MD Anderson, Pedro transitioned from academic cancer research to company-building through Deep Science Ventures. There, he partnered with bacterial engineer Annelise Soulier to develop Neobe’s core strategy: engineering bacteria to break down tumor barriers from within.

The Problem and the Opportunity

Cells, antibodies, and even small molecules have a very difficult time reaching the inner tumor.

Pedro explains that solid tumors aren’t just clumps of cancer cells – they’re embedded in a dense, fibrotic matrix that acts like a fortress, blocking immune cells and therapies from getting in.

This stiff extracellular environment also collapses blood vessels, reducing drug perfusion. As a result, even powerful treatments like CAR-T cells, antibodies, and chemo often fail to reach their targets.

Neobe’s goal is to break down these barriers, soften the tumor, and enable therapies to penetrate more deeply – turning inaccessible, treatment-resistant tumors into ones that can finally respond.

 

Shortcomings of Current Approaches

Degrading ECM in the tumor without causing toxicities has been a major challenge.

Previous attempts to break down the fibrotic “castle walls” of solid tumors – referring to the extracellular matrix (ECM) – have largely failed due to safety issues.

The ECM is a dense, cross-linked mesh of collagens and glycoproteins essential to all healthy tissues. Systemic delivery of ECM-degrading agents led to off-target effects, including cardiac and digestive damage.

Neobe was founded to solve this exact challenge: to break down the ECM only within the tumor, using localized, tumor-activated bacterial delivery, avoiding the collateral damage seen with earlier approaches.

Neobe's Unique Approach

Neobe uses genetically-engineered bacteria to “soften up” solid tumors…

Neobe Therapeutics leverages the natural tendency of bacteria to colonize solid tumors – regions that are hypoxic, nutrient-rich, and immune-privileged.

By engineering commensal-derived bacteria with synthetic biosensors, they create living “bioreactors” that detect the tumor microenvironment and locally secrete ECM-degrading enzymes.

This “Trojan horse” approach allows the bacteria to soften fibrotic tumors from the inside, improving immune cell infiltration and drug access without damaging healthy tissue or triggering systemic side effects.

How is Neobe's Approach Different?

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