SciTransfer
Organization

NEWCELLS BIOTECH LIMITED

UK biotech SME providing iPSC-derived human cell models for rare disease research, drug testing, and animal-free safety assessment.

Technology SMEhealthUKSMENo active H2020 projects
H2020 projects
3
As coordinator
0
Total EC funding
€880K
Unique partners
40
What they do

Their core work

Newcells Biotech is a UK-based SME specializing in human cell-based assays and disease models, with particular strength in iPSC-derived cell technologies. They provide advanced cellular models — including organoids and photoreceptor cells — that enable researchers to study disease mechanisms and test therapies without relying on animal models. Their work spans inherited eye diseases (Stargardt disease), ciliary disorders, and chemical safety assessment, positioning them as a supplier of human-relevant in vitro tools for both pharmaceutical and toxicology applications.

Core expertise

What they specialise in

iPSC-derived disease modelsprimary
3 projects

All three H2020 projects (in3, StarT, SCilS) involve human cell-based models for disease research or safety testing.

Inherited retinal disease biologyprimary
1 project

StarT project focuses specifically on Stargardt disease, involving photoreceptor cells, genome editing, and therapy development.

Animal-free safety assessmentsecondary
1 project

The in3 project developed integrated approaches to chemical and nanomaterial safety assessment without animal testing.

Cilia biology and ciliopathiesemerging
1 project

SCilS project (2020-2024) studies ciliary signalling in development and disease using organoids and multi-omics.

Multi-omics and functional genomicssecondary
2 projects

StarT and SCilS projects employ genomics, transcriptomics, and multi-omics approaches to dissect molecular disease mechanisms.

Evolution & trajectory

How they've shifted over time

Early focus
Animal-free safety testing
Recent focus
Rare genetic disease modelling

Newcells' earliest H2020 involvement (2017, in3) focused on replacing animal models in toxicology and chemical safety — a broad applications-driven effort. From 2018 onward, their work shifted decisively toward rare genetic diseases, first with inherited blindness (StarT, 2018) and then ciliopathies (SCilS, 2020), employing increasingly sophisticated molecular tools like genome editing, organoids, and multi-omics. The trajectory shows a clear move from general safety testing toward specialized rare disease modelling with deeper molecular characterization.

Newcells is deepening its focus on organoid-based rare disease models with multi-omics characterization, making them an increasingly valuable partner for precision medicine and gene therapy consortia.

Collaboration profile

How they like to work

Role: specialist_contributorReach: European14 countries collaborated

Newcells consistently participates as a partner rather than a coordinator, contributing specialized cell biology capabilities to larger training networks. With 40 unique partners across 14 countries from just 3 projects, they operate in sizeable international consortia (typical of MSCA training networks). This pattern suggests they are a trusted specialist contributor that larger academic groups bring in for their commercial cell model expertise.

Despite only 3 projects, Newcells has built a broad network of 40 partners across 14 countries, reflecting the large consortium structure of MSCA training networks. Their reach is genuinely pan-European, not concentrated in any single region.

Why partner with them

What sets them apart

Newcells occupies a niche at the intersection of commercial cell model provision and academic rare disease research — a combination few SMEs can offer. As a private company embedded in MSCA training networks, they bring industry-grade cell assay platforms to academic consortia studying conditions like Stargardt disease and ciliopathies. For consortium builders, they offer a ready-made bridge between fundamental disease biology and translatable human cell models.

Notable projects

Highlights from their portfolio

  • StarT
    Largest-funded project (EUR 303K) tackling Stargardt disease through a full pipeline from genomics to therapy development, combining genome editing with iPSC-derived photoreceptor models.
  • SCilS
    Most recent project (2020-2024) representing their current strategic direction toward organoid-based disease modelling with multi-omics characterization of ciliopathies.
  • in3
    Earliest project showing their foundational capability in animal-free chemical and nanomaterial safety assessment — a growing regulatory priority across Europe.
Cross-sector capabilities
Toxicology and chemical safety (animal-free testing)Pharmaceutical drug development (disease model provision)Environmental safety assessment (nanomaterial testing)Regenerative medicine (stem cell-derived tissues)
Analysis note: Profile based on only 3 projects, all as participant in MSCA training networks. The company's commercial product portfolio and full service range cannot be fully assessed from H2020 data alone. Keywords were absent from the earliest project (in3), limiting early-period keyword analysis. Website review would provide a more complete picture of their current capabilities.