A King's College London spin-out rebuilding the CAR-T receptor sideways - to reach the solid tumors that cell therapy has struggled to treat.
CAR-T therapy rewrote the rules for blood cancers. Engineer a patient's own T cells to recognize a tumor, infuse them back, and watch leukemias and lymphomas melt away. Then the field hit a wall: solid tumors - the lung, ovarian, and pancreatic cancers that make up the bulk of the disease - barely responded. Leucid Bio, a clinical-stage biotech founded in 2014 out of King's College London, was built around a specific answer to why.
The company's thesis starts with the receptor itself. Conventional CARs stack their signalling machinery in a linear, vertical column that projects out from the cell. Leucid's founder, Dr John Maher, spent more than 20 years arguing that nature does it differently: real immune receptors distribute their signalling domains laterally, alongside the cell membrane. Leucid Bio's proprietary Lateral CAR platform recapitulates that architecture. The internal shorthand is blunt - "build out, not down."
The claim is that a receptor closer to natural biology signals more faithfully: enhanced potency where you want it, reduced toxicity where you don't. It is an engineering argument, not a marketing one, and Leucid is now testing it in patients.
Redesigns the CAR so its signalling domains sit laterally alongside the membrane, mimicking natural immune receptors. The goal: higher potency, lower toxicity - "build out, not down."
An autologous CAR-T targeting NKG2D stress ligands - present on 80%+ of tumor cells - with an added CXCR2 mechanism to help cells infiltrate the tumor. Potentially tumor-agnostic.
Phase I/IIa dose-escalation study evaluating the safety and clinical activity of LEU011 in patients with refractory solid tumors. First patient dosed in 2025.
Solid tumors defend themselves. They hide behind a hostile microenvironment, limit which cells can get inside, and blunt the ones that do. Leucid's dual-mechanism design is built for exactly those obstacles - and its earliest clinical evidence came not from a scan but from a biopsy showing engineered cells inside the tumor.
Bars are illustrative of qualitative findings reported from the ongoing Phase I/IIa AERIAL trial (Nov 2025). Not precise measured values.
The model. Leucid Bio is a venture-funded, clinical-stage company - not yet a commercial one. It creates value by advancing its Lateral CAR pipeline through the clinic on specialist life-science capital, with eventual routes including partnership, licensing, or acquisition by a larger pharmaceutical company. Reported revenue reflects grants and early activity rather than product sales.
The customers. The ultimate beneficiaries are patients with refractory solid tumors - including platinum-resistant ovarian and other advanced cancers - treated through clinical trials at UK hospital sites. Near-term stakeholders are the investors, academic collaborators, and clinical investigators moving LEU011 forward.
The competition. Leucid works in a crowded field of solid tumor cell therapy - Celyad Oncology, Autolus, Adaptimmune, T-knife, and various academic NKG2D programs among them. Its differentiator is architectural: rather than a new target alone, it changes the shape of the receptor itself, betting that design - not dose - is what solid tumors have been waiting on.
CEO Filippo Petti joined in July 2023 after serving as CEO, CFO, and Executive Director of Celyad Oncology. He sits opposite scientific founder Dr John Maher, whose two decades of King's College London research the company exists to translate - the recurring pattern in good biotech: a founder who won't quit paired with an operator who has shipped before.
Led by Epidarex Capital with Vulpes Investment Management, 2Invest, Sofinnova Partners, and the British Business Bank's Future Fund.
Co-led by Epidarex Capital and 2invest AG - bringing the Series A to £18.7M and funding the start of the AERIAL trial.
Spun out of King's College London to commercialize two decades of Dr John Maher's CAR-T research.
Raised its first institutional round, led by Epidarex.
Former Celyad Oncology CEO/CFO joins to drive the company toward the clinic.
Closed £7.2M Series A1 and treated the first patient in the AERIAL trial of LEU011.
Reported tumor infiltration, disease control at the lowest dose, and a well-tolerated safety profile; presented at SITC 2025.
The design mantra is literally "build out, not down" - signalling domains placed sideways, not stacked.
NKG2D ligands, LEU011's target, appear on more than 80% of human tumor types - making the approach potentially tumor-agnostic.
The whole company grew from the work of one scientist, Dr John Maher, over 20+ years.
The clearest early clinical proof came from a biopsy showing engineered cells inside a tumor - not a scan.
Its tagline puns on its science: "Thinking laterally about CAR-T."
It develops next-generation CAR-T cell therapies for refractory solid tumors using its proprietary Lateral CAR platform, which redesigns the CAR receptor to mimic natural immune receptors.
A CAR-T engineering approach that positions the receptor's signalling domains laterally alongside the cell membrane rather than in a linear stack, aiming for higher potency and lower toxicity - the company calls it "build out, not down."
Leucid Bio's lead autologous CAR-T candidate, targeting NKG2D stress ligands (found on 80%+ of tumors) plus CXCR2 signalling, currently in the Phase I/IIa AERIAL trial for refractory solid tumors.
It was founded in 2014 on Dr John Maher's research at King's College London; Maher is Chief Scientific Officer and Filippo Petti has been CEO since July 2023.
It has raised its Series A to £18.7M to date - an initial £11.5M in 2021 and a £7.2M Series A1 first close in February 2025 - backed by Epidarex Capital, 2invest, Sofinnova Partners, Vulpes, and the British Business Bank's Future Fund.
Video: Leucid Bio has not published an official YouTube channel or product-demo video at the time of writing. Search "Leucid Bio" or "John Maher CAR-T" on YouTube for related conference talks and interviews.