Cellular Therapeutics
Living-cell preparations developed for their capacity to interact with tissues, immune systems and local biological environments. This category includes MSC-based and selected immune-cell technologies.
Cellular, cell-free and immune biotechnology platforms
EspañolCELLMEX develops and evaluates cellular, cell-free and immune-based biotechnology platforms. Our work includes mesenchymal stromal cells, extracellular vesicles, secretome-derived preparations, conditioned-media technologies, lineage-directed cells and selected immune-cell applications.
Regenerative medicine encompasses several distinct biological approaches. These include living-cell therapies, cell-free signalling products, tissue-directed cellular systems and immune-cell technologies.
Each platform has a different biological identity, proposed mechanism, manufacturing process, characterisation strategy and clinical purpose.
For this reason, CELLMEX does not treat terms such as stem cells, exosomes, secretome and conditioned media as interchangeable.
Each technology requires its own scientific, clinical, quality and regulatory assessment.
The CELLMEX technology portfolio is organised into cellular therapeutics, cell-free biologics and advanced cellular development platforms.
Living-cell preparations developed for their capacity to interact with tissues, immune systems and local biological environments. This category includes MSC-based and selected immune-cell technologies.
Preparations derived from cellular signalling products rather than intact living cells. These may include extracellular vesicles, soluble mediators and defined secretome fractions.
Technologies involving directed cellular differentiation, tissue-specific phenotypes, specialised manufacturing processes and translational research applications.
Select a technology to review its biological basis, manufacturing considerations, proposed applications, characterisation requirements and clinical context.
Mesenchymal stromal cell platforms developed for their immunomodulatory, anti-inflammatory, trophic and tissue-supporting biological activity.
Highly enriched extracellular-vesicle preparations intended to separate vesicular signalling components from broader conditioned-media constituents.
Nano-scale extracellular-vesicle populations released by cells and studied as mediators of intercellular communication and biological signalling.
The complete group of soluble and vesicular factors released by mesenchymal stromal cells under defined culture conditions.
Cell-culture medium collected after exposure to living cells and containing a mixture of soluble proteins, metabolites and extracellular particles.
Conditioned-media preparations processed to reduce or remove selected extracellular-vesicle fractions while retaining soluble secreted factors.
Mesenchymal stromal cells guided toward selected tissue-associated phenotypes through controlled culture, signalling and differentiation protocols.
Cellular platforms involving the isolation, activation, expansion or functional modification of selected immune-cell populations.
Each technology requires a defined development pathway before it can be responsibly positioned for research, clinical evaluation or commercial use.
Establish the source material, intended product identity and biological classification.
Define culture, isolation, purification, concentration and storage conditions.
Confirm identity, composition, purity, viability, potency and relevant quality attributes.
Evaluate the biological rationale, supporting evidence, route of administration and target use.
Assess manufacturing controls, documentation, safety requirements and applicable regulatory pathways.
The presence of a technology on this website does not establish that it is approved, clinically proven or suitable for every patient or medical condition.
Some cellular and immune-cell therapies have established uses in specific medical settings. Other applications involving MSCs, extracellular vesicles, exosomes, secretome products, conditioned media or differentiated cells remain investigational or require additional clinical validation.
Product identity, source material, manufacturing, characterisation, potency, safety, intended use and applicable regulatory requirements must be evaluated separately for each technology.
Detailed pages will provide additional scientific, manufacturing, quality and clinical information for each platform.