NHP(monkey) Disease Models

NHP(monkey) Disease Models

Prisys offers essential non-human primate (NHP) models for biomedical research, bridging basic research and clinical applications. Our expertise ensures high fidelity to human biology, providing accurate and reproducible results for drug discovery and development.
Product Introduction

Non-human primate (NHP) models are essential tools in basic research, drug discovery, and development. Their close genetic, anatomical, and physiological similarities to humans make them invaluable for studying human diseases and developing new treatments. NHP models provide critical insights that bridge the gap between basic research and clinical applications, ensuring that findings can be translated effectively into medical advancements. Despite the progress in in vitro methods, NHP models remain irreplaceable for human translational research.

 
 
 
 
 
 
 
 

Prisys's Approach and Expertise

 

Prisys excels in developing and utilizing NHP models, particularly induced and surgical models. Our expertise spans multiple research areas such as immunology , cardiovascular , respiratory , neurological , and metabolic diseases . We employ physical methods (e.g., mechanical, surgical, gene editing) to create phenotypes that closely resemble human conditions. For instance, ischemic events can be surgically induced to study stroke survival or cardiac reperfusion post-heart attack. 

Prisyss Approach and Expertise
Prisys's Approach and Expertise

 

Prisys's NHP Models

 

At Prisys, we recognize the vital role that NHP models play in biomedical research. With extensive experience and expertise, we offer a comprehensive range of NHP models tailored to meet the diverse needs of our global clients. Our scientists are dedicated to assisting you in selecting the most appropriate model for your research, ensuring high fidelity to human biology for accurate and reproducible results.

 

Prisys is committed to advancing scientific research by providing top-quality NHP models and expertise. Please click on the links below to access our signature NHP models or contact our scientists to customize your own models.

 

Immunology Delayed-type Hypersensitivity Hepatology Liver steatosis/ NASH/MASH Ophthalmology Experimental Autoimmune Uveitis/EAU
Rheumatoid Arthritis/CIA Acute Liver Injury Glaucoma
Osteoarthritis Drug-induced Liver Injury Retinitis Pigmentosa
Multiple Sclerosis/EAE Liver Fibrosis Retinal Neovascularization
Inflammatory Bowel Disease (UC) Portal hypertension Gynecology Post-Partum Hemorrhage
Psoriasis Cholelithiasis Endometriosis
Pruritus Intrahepatic Carcinoma Co-develop Systemic Lupus Erythematosus/SLE
Atopic Dermatitis Nephrology Acute Kidney Injury Sjögren's Syndrome
T-cell-Dependent Antibody Response Renal Fibrosis Autoimmune Myositis
Immunosuppression Chronic Kidney Disease Crohn's Disease
FSGS Myasthenia Gravis
Hematology Hemophilia A IgA Nephropathy/IgAN Alzheimer's Disease
Endotoxemia Renal Transplantation Amyotrophic Lateral Sclerosis
Arterial Thrombosis Huntington's Disease
Venous Thrombosis Metabolism
(Complications)
Type I Diabetes Diabetic retinopathy
Anemia Type II Diabetes Myopia
A-V Shunt Insulin Resistance Thrombocytopenic Purpura
Bleeding models Hyperlipidemia Acute Respiratory Distress syndrome/ARDS
Acute Blood Loss/Shock Hypercholesterolemia Liver Transplantation
Wound healing Acute hypertension Intestinal Cancer
Cardio-vascular Acute Myocardial Infarction Obesity Lung Cancer
Heart Failure Respiratory Acute Lung inflammation Breast Cancer
Pulmonary Artery Hypertension Asthma Brain Glioma
Pulmonary Artery Embolism COPD Sleep Apnea/hypopnea
Cardio-renal syndrome Pulmonary Embolisation Endometrial Injury induced Infertility
Neurology Intracerebral Hemorrhagic Stroke Pulmonary arterial hypertension    
Brain Ischemic Stroke/MCAO Lung Fibrosis    
Parkinson's Disease Allergic Rhinitis    
Pain Models        
Epilepsy        
Drug induced hallucination    

 

 

Customized Model Development

In addition to our existing models, we continuously improve our technology to develop new animal models that meet the evolving needs of our clients. In our history about 30% novel NHP models were generated, refined, and stabilized through a special mechanism call "Co-develop", where joint efforts and combined expertise from Prisys and collaborators were invested to develop NHP models with mutual interests. The development, aiming at offering a better tailored solution to assess drug pharmacology, was routinely initiated with a small pilot proof-of-concept study then followed by a bigger therapeutic project. For more detailed information or to consult with our scientists, please contact us directly.

 

 

 

Progression of kidney fibrosis post-UUO, with Masson's trichrome staining
Progression of kidney fibrosis post-UUO, with Masson's trichrome staining

Goals of In Vivo Efficacy Models

 

Determining whether a compound can produce the desired physiological response.

Comparing the impact of various doses of the same compound.

Evaluating the efficacy of different compounds relative to each other.

 

Efficacy in in vivo models is typically measured by the dose provided and the percentage effect relative to the maximal effect achievable. The most commonly reported value is the ED50, the dose at which 50% of the maximum effect is observed. These values are crucial for ranking compounds within a specific in vivo model.

 

 

Prisys is committed to advancing scientific research by providing top-quality NHP models and expertise. Please click on the link below to access our off-the-shelf models or contact our scientists to customize your own model. For more detailed information on our models or to consult with our scientists, please explore our library of models or contact us directly.

 

 

Contact Us for More Info

 

 

 
 
 
 
 
 

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