BRIDGING THE GAP BETWEEN PRECLINICAL AND CLINICAL DATA USING HUMAN ASSAYS
REVEAL THE REAL POTENTIAL OF YOUR DRUG DISCOVERY PROGRAM USING HUMAN STANDARDIZED DISEASE MODELS
Human Cell Design is a Contract Research Organization which combines a unique 2D/3D human disease models panel with high expertise in human cell biology and physiology. We provide customized solutions for accelerating clinically relevant scientific progress. From target validation to preclinical validation our experts provide you with long term strategies and help you develop stables readouts and valuable deliverables. We share the same goal by generating robust data to independently leverage your project real potential.
GET MORE INFORMATION ON HUMAN CELL DESIGN SERVICE EXPERTISE
CUSTOM PRE-CLINICAL SERVICES DEDICATED TO DRUGS TARGETING TYPE I AND 2 DIABETES
TYPE 1 & 2 DIABETES:
- Target Validation
- Glucolipotoxicity
- Inflammation mediated diabetes
- Immuno-dependant beta cell destruction
- Insulin Secretion
- 3D sphere model
GET MORE INFORMATION ON HUMAN CELL DESIGN SERVICE EXPERTISE
CUSTOM PRE-CLINICAL SERVICES DEDICATED TO DRUGS TARGETING TYPE I AND 2 DIABETES
TYPE 1 & 2 DIABETES:
Target Validation
Glucolipotoxicity
Inflammation mediated diabetes
Immuno-dependant beta cell destruction
Insulin Secretion
3D sphere model
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Dr. Thomas Frogne
NOVO NORDISK
The EndoC-βH1 cell line is a valid model of human beta cells and applicable for screenings to identify novel drug target candidates.
MOLECULAR METABOLISM
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Dr. Norbert Tennagels
SANOFI
Acute and repeated treatment with 5-PAHSA or 9-PAHSA isomers does not improve glucose control in mice.
CELL METABOLISM
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Dr. Pia Davidsson
ASTRAZENECA
Secretagogin is increased in plasma from type 2 diabetes patients and potentially reflects stress and islet dysfunction.
PLOS ONE
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Dr. Axel Haup
ELI LILLY
LY3298176, a novel dual GIP and GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus: From discovery to clinical proof of concept.
MOLECULAR METABOLISM
TRULY TRANSLATIONAL HUMAN CELL MODELS
GETTING BETTER MEDICATION TO PATIENTS FASTER
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Here at Human Cell Design, we are convinced that human cell models are the way forward to getting better medication to patients faster. Our customers in the pharmaceutical and biotech industries and in academia rely on our internationally recognized human cells to generate reproducible data and to make informed decisions early in the drug development process.
VALIDATED BY OVER
INTERNATIONAL INSTITUTIONS
Accelerate and secure your Drug Discovery program using unique standardized disease models and assays
ROBUST
SCALABLE
DISEASE RELEVANT
PHYSIOLOGICAL
SENSITIVE
DATA REPRODUCIBILITY
A PATENTED CELL MATURATION PLATFORM
FOR LARGE-SCALE PRODUCTION OF FUNCTIONAL HUMAN CELLS
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To overcome industrial bottlenecks and provide truly translational human cell models for R&D, Human Cell Design combines the potential of human iPSC technology or human primary cells with a patented maturation platform. Our NatLine Platform® amplifies and maturates hiPSC-derived and primary progenitor cells to provide unlimited quantities of truly mature and functional human cells. The produced terminally differentiated cells replicate native adult human cells. NatLine® platform is adapted to large-scale and reproducible production of healthy or diseased human cell models.
LATEST NEWS
Immunology Diabetes Study 2024 Conference Poster
20th Annual Congress of the Immunology Diabetes Study congress (IDS 2024): Discover the Human Cell Design poster. Human Cell Design has participated in the 20th IDS congress in Bruges (Belgium). During the ...
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Human Cell Design was present in China to meet you and discover your projects. Our expert was in China during 8 days with our exclusive distributor Lab Direct. We were delighted to meet our Chinese customers ...
Read moreEuropean Association for the Study of Diabetes 2024 Conference
60th Annual Congress of the European Association for the Study of Diabetes (EASD): Human Cell Design was present to meet you and discover your projects. Scientists from Human Cell Design participated in the ...
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