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Innovative translational models are essential to accurately predict central nervous system (CNS) therapeutic outcomes – providing a robust dataset to derisk drug development. Our team of expert neuroscientists bring decades of experience leveraging human iPSC-derived systems, rodent primary CNS cells and organotypic models to accelerate your journey from target to optimized lead.
Collaborating with you to meticulously craft customized assays that exactly meet your project needs is our speciality, providing solutions to the most complex challenges. Our cutting-edge technologies, comprehensive quantitative readouts, and consultative approach provide the high-quality data required to confidently progress toward the clinic.
Formerly Aquila Biomedical, we pioneered translational neuroscience assays and continue to support clients in developing breakthrough CNS therapies.
We understand that neuroscience is one of the most complex therapeutic areas. Developing therapies to address longstanding challenges, such as neurodegeneration, demands deep expertise and specialized solutions to translate research into real-world impact.
To support your journey through the discovery and preclinical development of novel CNS therapeutics, we harness in vitro and ex vivo models of increasing physiological relevance and complexity to craft unique assays. For novel challenges, we design bespoke approaches grounded in decades of neurobiological expertise.

Our team of neuroscientists have deep expertise in:
By seamlessly combining rodent and human iPSC-derived models, we deliver robust pre-clinical data for your drug discovery program.
Neuroinflammation is a central feature of neurodegenerative diseases. Multiple astrocytes and microglia signalling pathways become chronically dysregulated, triggering excessive and continued release of pro-inflammatory cytokines, chemokines, and neurotoxic molecules, contributing to neuronal damage and degeneration.
Modulation of these inflammatory pathways is a promising strategy for the treatment of neurodegenerative diseases such as Alzheimer’s disease and Parkinson’s disease.
Are you looking for ready-made solutions or bespoke experimental designs? Our neuroscientists will be able to support your goals.
The maintenance of healthy myelin is essential for fast and efficient conduction of action potentials along axons. Oligodendrocyte precursor cells (OPCs) are a self-renewing cell population that gives rise to mature oligodendrocytes, the myelin-producing cells of the central nervous system.
OPC dysfunction and myelin loss can lead to severe neurological conditions, such as multiple sclerosis, and contribute to a broader spectrum of neurodegenerative conditions, including Alzheimer’s disease.
Restoration of normal OPC and myelin function is a key target for neurotherapeutics. In the presence or absence of candidate therapeutics, we can quantify:

The aim of any candidate CNS drug is to improve neuronal function and signalling pathways. In vitro neuronal models offer a controlled and reproducible system to study the effects of candidate drugs.
Neuronal monocultures are ideal to investigate the impact of a drug on cell-autonomous functions and pathways, or to reveal its potential neurotoxic or neuroprotective effects.
In contrast, neuron–glia co-cultures enable assessment of drug candidates that act indirectly on neurons by modulating glial activity or regulating neuron–glia communication. These co-culture systems offer a more physiologically relevant environment for evaluating neuroactive compounds and their mechanisms of action.
Thanks to our expertise in neurobiology and neurophysiology, we can guide you towards the most appropriate cell model, experimental design and readout to provide you with the answers you need.
Our expertise includes:
Our specialist neuroscience expertise is complemented by a wider offering across chemistry, ADMET, and GMP manufacturing services. Speak to our team to explore how we can help you bring your immunology therapeutic to the clinic.