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List of pathological models

Table of Contents
Table of Contents

Disease Area-Specific Model Animal Review List

This page organizes widely referenced model animal review articles in each disease area, considering both classic reviews with high citation counts and recent reviews.

Please use this as reference information for model selection in non-clinical studies. (As of the survey on March 30, 2026)

MASH / NASH・Liver Fibrosis・HCC

MASH is a disease characterized by the continuous progression of lipid metabolism abnormalities, inflammation, and fibrosis, and is an area difficult to replicate with a single model.

Classic review

Latest reviews

In this field, evaluation by combining diet-induced, toxicity-induced, and genetically modified models is considered important.

Liver disease (acute injury/fibrosis)

Models and evaluation metrics used differ significantly between acute liver injury and chronic fibrosis.

Classic review

Latest reviews

In recent years, the importance of selecting models with translational properties in mind has been emphasized.

Pulmonary Fibrosis / IPF

IPF is a disease area where the balance between reproducibility and clinical correlation is important.

Classic review

Latest reviews

In recent years, there has been growing interest in chronic models and humanized models.

CKD / Renal Fibrosis

In kidney disease, surgical models and metabolic models are used in combination.

Classic review

Latest reviews

In recent years, the introduction of humanized models and 3D culture systems has been advancing.

Metabolic diseases (obesity, diabetes)

In metabolic diseases, it is important to choose between genetic and dietary models.

Classic review

Latest reviews

Animal models for type 1 and type 2 diabetes: advantages and limitations Frontiers in Endocrinology (2024): https://pubmed.ncbi.nlm.nih.gov/38444587/

When selecting models, it is important to consider metabolic differences with humans.

Inflammatory Bowel Disease (IBD)

Inflammation models vary greatly depending on the induction method.

Classic review

Latest reviews

In recent years, models combining human gut microbiota have also been attracting attention.

Cancer / Tumor models

Tumor models are selected according to the purpose of evaluation.

Classic review

Latest reviews

In recent years, the importance of evaluation using PDX and humanized models has been increasing.

Summary

Key points common to all disease areas:

By referring to these review papers, more appropriate model selection and trial design will be possible.

List of pathological models used in non-clinical studies

Central nervous system (brain)

Model Target disease/phenotype Major CRO Original paper/Published review
APP/PS1 Tg (B6;C3-Tg(APPswe,PSEN1dE9)) Alzheimer's Disease (Amyloid Plaques, Cognitive Impairment) Biospective / Taconic Biosciences Mutant presenilins specifically elevate the levels of the 42-amino acid β-amyloid peptide in vivo: evidence for augmentation of a 42-specific γ secretase
Human Molecular Genetics, 13(2):159–170, 2004
alpha-synuclein A53T Tg Parkinson's disease (Lewy bodies, motor impairment) Biospective / Scantox / The Jackson Laboratory Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein
Neuron, 34(4):521–533, 2002
SCN1A+/- Dravet Model Dravet syndrome (seizures, developmental delay) The Jackson Laboratory Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy
Nature Neuroscience, 9(9):1142–1149, 2006
icv-STZ Alzheimer's Disease (Neuroinflammation) SMC Laboratories Intracerebroventricular administration of streptozotocin causes long-term diminutions in learning and memory abilities and in cerebral energy metabolism in adult rats
Behavioural Neuroscience, 112(5):1199–1208, 1998
EAE (Mog-induced) Multiple sclerosis-like (demyelinating encephalomyelitis) MD Biosciences A myelin oligodendrocyte glycoprotein peptide induces typical chronic experimental autoimmune encephalomyelitis in H-2b mice
European Journal of Immunology, 25(7):1951–1959, 1995

Cardiovascular system

Model Target disease/phenotype Major CRO Original paper/Published review
ApoE−/− DECK Arteriosclerosis (hyperlipidemia, plaque formation) Charles River / Taconic Biosciences Spontaneous hypercholesterolemia and arterial lesions in mice lacking apolipoprotein E
Science, 258(5081):468–471, 1992
LDLR−/− DECK Arteriosclerosis (Cholesterol Metabolism Disorder) The Jackson Laboratory Massive xanthomatosis and atherosclerosis in cholesterol-fed low-density lipoprotein receptor-negative mice
Journal of Clinical Investigation, 93(5):1885–1893, 1994
Continuous Angiotensin II Infusion Hypertension (elevated blood pressure, cardiac hypertrophy) - Angiotensin II promotes atherosclerotic lesions and aneurysms in apolipoprotein E-deficient mice
Journal of Clinical Investigation, 105(11):1605–1612, 2000
Acute myocardial infarction (LAD ligation) Myocardial infarction (myocardial necrosis, decreased cardiac function) - Experimental myocardial infarction. I. A method of coronary occlusion in small animals
Annals of Surgery, 140(5):675–682, 1954

Liver

Model Target disease/phenotype Major CRO Original paper/Published review
Carbon tetrachloride Liver fibrosis/cirrhosis Melior Discovery / SMC Laboratories Carbon tetrachloride hepatotoxicity: an example of lethal cleavage
CRC Critical Reviews in Toxicology, 2(3):263–297, 1973
WD+CCl4 Liver fibrosis/cirrhosis SMC Laboratories Carbon tetrachloride (CCl4) accelerated the development of non-alcoholic fatty liver disease (NAFLD)/steatohepatitis (NASH) in MS-NASH mice fed a western diet supplemented with fructose (WDF).
BMC Gastroenterology, 20:339, 2020
High-fat diet (HFD) MAFLD/MASLD (Fatty Liver, Inflammation, Early Fibrosis) Charles River / Taconic High-fat diets: modeling the metabolic disorders of human obesity in rodents
Obesity, 15(4):798–808, 2007
MCD, CDAHFD diet MASH model (Metabolic dysfunction-Associated Steatohepatitis) SMC Laboratories / Gubra An improved mouse model for rapid development of fibrosis in non-alcoholic steatohepatitis
International Journal of Experimental Pathology, 94(2):93–103, 2013
TAA Liver fibrosis/cirrhosis SMC Laboratories The induction of liver cancer by chemicals
Cancer Research, 6:245–250, 1946
Bile duct ligation (BDL) Cholestatic liver disease (PBC/PSC) SMC Laboratories Bile duct ligation in mice: induction of inflammatory liver injury and fibrosis by obstructive cholestasis
Journal of Visualized Experiments, (96):e52438, 2015
DDC food Biliary hepatitis/fibrosis SMC Laboratories A New Xenobiotic-Induced Mouse Model of Sclerosing Cholangitis and Biliary Fibrosis
American Journal of Pathology, 171(2):525–536, 2007
ANIT Biliary hepatitis/fibrosis SMC Laboratories Drug- and chemical-induced intrahepatic cholestasis
Pharmacological Reviews, 28(3):207–273, 1976
Wilson's Disease Model (Atp7b−/−) Wilson's Disease (Copper Metabolism Disorder, Liver Damage) - Null mutation of the murine ATP7B gene results in copper accumulation and liver disease
PNAS, 96(23):13312–13317, 1999
STAM (Type 2 Diabetes + MASH) T2D with MASH SMC Laboratories A murine model for non-alcoholic steatohepatitis showing evidence of association between diabetes and hepatocellular carcinoma
Medical Molecular Morphology, 46(3):141–152, 2013

Metabolic and inflammatory hepatocellular carcinoma

Model Target disease/phenotype Major CRO Original paper/Published review
STAM-IO (STZ + HFD) MASH-HCC under normal immunity (tumor microenvironment with fibrosis; immune response evaluation) SMC Laboratories A murine model for non-alcoholic steatohepatitis showing evidence of association between diabetes and hepatocellular carcinoma
Medical Molecular Morphology, 46(3):141–152, 2013
CDAHFD-induced HCC model Spontaneous hepatocellular carcinoma formation from MASH with severe inflammation and fibrosis SMC Laboratories / Gubra An improved mouse model for rapid development of fibrosis in non-alcoholic steatohepatitis
International Journal of Experimental Pathology, 94(2):93–103, 2013
Western Diet + CCl₄ Model (WD+CCl₄) Progression from NASH with advanced fibrosis to HCC SMC Laboratories Carbon tetrachloride (CCl4) accelerated the development of non-alcoholic fatty liver disease (NAFLD)/steatohepatitis (NASH) in MS-NASH mice fed a western diet supplemented with fructose (WDF).
BMC Gastroenterology, 20:339, 2020
DEN+CCl₄ model Fibrotic background HCC (chronic liver injury + chemical carcinogenesis; tumorigenesis with liver cirrhosis) SMC Laboratories The DEN and CCl4-Induced Mouse Model of Fibrosis and Inflammation-Associated Hepatocellular Carcinoma
Current Protocol, 1(8):e211

Kidney

Model Target disease/phenotype Major CRO Original paper/Published review
db/db (Lepr−/−) Type 2 diabetic nephropathy (obesity, hyperglycemia) The Jackson Laboratory / Charles River Laboratories / Taconic Biosciences Evidence that the diabetes gene encodes the leptin receptor: identification of a mutation in the leptin receptor gene in db/db mice
Cell, 84(3):491–495, 1996
NOD mouse Type 1 diabetes (autoimmune destruction of pancreatic beta cells) The Jackson Laboratory / Taconic Biosciences Breeding of a non-obese, diabetic strain of mice
Experimental Animals, 29(1):1–13, 1980
OVE26 (T1D) Type 1 diabetes model (insulin deficiency) - Calmodulin-induced early-onset diabetes in transgenic mice
Cell, 58(6):1067–1073, 1989
Akita (Ins2+/-) Type 1 Diabetes (Hereditary Insulin Deficiency) The Jackson Laboratory A novel locus, Mody4, distal to D7Mit189, contributes to early-onset NIDDM in nonobese C57BL/6 (Akita) mutant mice
Diabetes, 46(5):887–894, 1997
eNOS−/− + db/db Hypertensive diabetic nephropathy - Diabetic endothelial nitric oxide synthase knockout mice develop advanced diabetic nephropathy
Journal of the American Society of Nephrology, 18(2):539–550, 2007
Polycystic kidney disease (Pkd1 KO) Autosomal dominant polycystic kidney disease (ADPKD) The Jackson Laboratory Perinatal lethality with kidney and pancreas defects in mice with a targeted Pkd1 mutation
Nature Genetics, 17(2):179–181, 1997
Alport syndrome (Col4a3−/−) Alport syndrome (abnormal glomerular basement membrane) The Jackson Laboratory Collagen COL4A3 knockout: a mouse model for autosomal Alport syndrome
Genes & Development, 10(23):2981–2992, 1996
Lupus Nephritis (NZB/NZW F1) Systemic lupus erythematosus (nephritis) The Jackson Laboratory Spontaneous autoimmune disease in NZB/NZW mice
Proceedings of the University of Otago Medical School, 37:9–11, 1967

Lung

Model Target disease/phenotype Major CRO Original paper/Published review
OVA asthma induction model Allergic asthma (eosinophilic airway inflammation) Charles River Laboratories / Inotiv OVA-Induced Allergic Airway Inflammation Mouse Model
Methods in Molecular Biology, 1916:297–301, 2019
HDM asthma model Allergic airway inflammation Charles River Laboratories / Inotiv Continuous exposure to house dust mites causes chronic inflammation and structural changes in the airways.
American Journal of Respiratory and Critical Care Medicine, 169(3):378–385, 2004
Bleomycin-induced pulmonary fibrosis Pulmonary fibrosis (interstitial pneumonia) SMC Laboratories The pathogenesis of bleomycin-induced pulmonary fibrosis
American Journal of Pathology, 77(2):185–197, 1974
Silicosis Pulmonary fibrosis (interstitial pneumonia) SMC Laboratories Silicosis: A Review of Experimental Studies
American Journal of Pathology, 49(5):819–846, 1966
COVID-19 model SARS-CoV-2 infection (ARDS-like lung injury) Charles River Laboratories / The Jackson Laboratory SARS-CoV-2 infection of human ACE2-transgenic mice causes severe lung inflammation and impaired function
Nature Immunology, 21(11):1327–1335, 2020

Gastrointestinal tract

Model Target disease/phenotype Major CRO Original paper/Published review
DSS colitis Inflammatory bowel disease (Ulcerative colitis) SMC Laboratories / Gubra A novel method for inducing experimental ulcerative colitis in mice
Gastroenterology, 98(3):694–702, 1990
TNBS colitis Crohn's disease-like colitis Charles River Laboratories / Inotiv Hapten-induced model of chronic inflammation and ulceration in the rat colon
Gastroenterology, 96(3):795–803, 1989
IL-10KO colitis Spontaneous Colitis (Chronic Inflammation) The Jackson Laboratory Interleukin-10 deficient mice develop chronic enterocolitis.
Cell, 75(2):263–274, 1993
Helicobacter pylori infection Chronic gastritis - Helicobacter bilis-associated inflammatory bowel disease in defined microbiota mice
Infection and Immunity, 72(6):3328–3337, 2004
AOM/DSS Colorectal Cancer Colorectal cancer (inflammation-related cancer) Crown Bioscience / Charles River Laboratories / SMC Laboratories Development of an inflammation-associated colorectal cancer model
Carcinogenesis, 33(5):875-882, 2012

Endocrine and Metabolic System

Model Target disease/phenotype Major CRO Original paper/Published review
ob/ob−/−) Obesity-type 2 diabetes The Jackson Laboratory / Taconic Biosciences Positional cloning of the mouse obese gene and its human homologue
Nature, 372(6505):425–432, 1994
db/db (Lepr−/−) Obesity-type 2 diabetes The Jackson Laboratory / Charles River Laboratories Evidence that the diabetes gene encodes the leptin receptor
Cell, 84(3):491–495, 1996
Diet-induced obesity (DIO) Obesity and metabolic syndrome Charles River Laboratories / Taconic Biosciences / Gubra / SMC Laboratories High-fat diets: modeling the metabolic disorders of human obesity in rodents
Obesity, 15(4):798–808, 2007
NOD mouse Type 1 diabetes (autoimmune) The Jackson Laboratory Breeding of a non-obese, diabetic strain of mice
Experimental Animals, 29(1):1–13, 1980
Neonatal STZ model Type 2 diabetes (beta-cell dysfunction) SMC Laboratories Studies on the diabetogenic action of streptozotocin
Cancer Chemotherapy Reports, 29:91–98, 1963

Immune and hematopoietic system

Model Target disease/phenotype Major CRO Original paper/Published review
NZB/NZW F1 (SLE) Systemic lupus erythematosus (lupus nephritis, etc.) The Jackson Laboratory Spontaneous autoimmune disease in NZB/NZW mice
Proceedings of the University of Otago Medical School, 37:9–11, 1967
MRL/lpr (SLE) SLE (Lymphadenopathy, Cutaneous Renal Lesions) The Jackson Laboratory Lymphoproliferation disorder in mice explained by defects in Fas antigen
Nature, 356(6367):314–317, 1992
RA (Rheumatoid Arthritis) Rheumatoid arthritis model (synovitis, bone destruction) Inotiv / Charles River Laboratories Autoimmunity to type II collagen: an experimental model of arthritis
Journal of Experimental Medicine, 146(3):857–868, 1977
K/BxN CAIA Autoimmune arthritis (antibody-mediated) - Organ-specific autoimmune disease
Cell, 87(5):811–822, 1996
NSG (NOD/SCID/γc)−/−) Severe Combined Immunodeficiency (T/B/NK cell deficiency) The Jackson Laboratory NOD/SCID/γcnull mouse: an excellent recipient mouse model for engraftment of human cells
Blood, 100(9):3175–3182, 2002
SCID (CB-17) Severe combined immunodeficiency Charles River Laboratories / Taconic Biosciences A severe combined immunodeficiency mutation in mice
Nature, 301(5900):527–530, 1983

Musculoskeletal system

Model Target disease/phenotype Major CRO Original paper/Published review
mdx (DMD) Duchenne muscular dystrophy CLEA Japan X chromosome-linked muscular dystrophy (mdx) in the mouse
Proceedings of the National Academy of Sciences USA, 81(4):1189–1192, 1984
D2.mdx (Severe DMD) Severe DMD The Jackson Laboratory Genetic background affects satellite cell properties and mdx phenotypes
American Journal of Pathology, 176(5):2414–2424, 2010
COL6 deficiency disorder Congenital muscular dystrophy - Collagen VI deficiency induces early onset myopathy in the mouse
Proceedings of the National Academy of Sciences USA, 95(3):1046–1051, 1998
Osteoporosis (OVX) Estrogen deficiency osteoporosis Charles River Laboratories / Inotiv The ovariectomized rat model of postmenopausal bone loss
Bone and Mineral, 15(3):175–191, 1991

Skin

Model Target disease/phenotype Major CRO Original paper/Published review
Imiquimod model Psoriasiform dermatitis (erythema, scaling) Charles River Laboratories / Inotiv / SMC Laboratories Imiquimod-induced psoriasis-like skin inflammation
Journal of Immunology, 182(9):5836–5845, 2009
North Carolina / Nigeria Atopic dermatitis (pruritic eczema, elevated IgE) Charles River Laboratories, Inc. NC/Nga mice: a model for atopic dermatitis
Int Arch Allergy Immunol, 120(Suppl 1):70–75, 1999
Bleomycin-induced pulmonary fibrosis Systemic sclerosis (SSc) SMC Laboratories Animal model of sclerotic skin. I: Local injections of bleomycin induce sclerotic skin mimicking scleroderma
Journal of Investigative Dermatology, 112(4):456–462, 1999
Contact dermatitis (DNFB) Contact dermatitis (allergic inflammation) Inotiv A hapten-induced model of allergic contact dermatitis characterized by T cell–mediated skin inflammation following sensitization and challenge with DNFB.

Reproductive and Endocrine Systems

Model Target disease/phenotype Major CRO Original paper/Published review
DHEA model (PCOS) Polycystic Ovary Syndrome (PCOS) - Effect of dehydroepiandrosterone and Δ4-androstenedione on the reproductive organs of female rats: induction of cystic changes in the ovary.
Nature, 1962;196:42–43.
Letrozole model (PCOS) PCOS - Letrozole-induced polycystic ovaries in the rat: a new model for cystic ovarian disease.
Archives of Medical Research, 2004;35(2):103–108.
Endometriosis model Endometriosis - Studies on the Surgical Induction of Endometriosis in the Rat
Fertility and Sterility, 1985;44(5):684–694.
GnRH receptor KO Hypogonadism (amenorrhea, infertility) - Mouse model of surgically induced endometriosis by autotransplantation of uterine tissue.
Journal of Visualized Experiments, 2012;(59):e3396

Sensory organs, development, and aging

Model Target disease/phenotype Major CRO Original paper/Published review
rd1 (Pde6bround 1) Retinitis pigmentosa (blindness) The Jackson Laboratory Mutations in the GnRH receptor gene: a new cause of autosomal recessive hypogonadotropic hypogonadism.
Archives of Medical Research, 1999;30(6):481–485.
Cx26 KO Hereditary hearing loss - Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death.
Current Biology, 2002;12(13):1106–1111.
Ames dwarf (Prop1)df/df) Laron Syndrome Model (GH Deficiency) The Jackson Laboratory Genotyping the Prop-1 mutation in Ames dwarf mice.
Mechanisms of Ageing and Development, 2001;122(15):1915–1918.
Zmpste24−/− HGPS Hutchinson-Gilford syndrome (progeria) - Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect.
Proceedings of the National Academy of Sciences USA, 2002;99(20):13049–13054.
Werner (Wrn−/−) Werner syndrome (progeria) - Metabolic and Phenotypic Differences Between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice.
PLoS ONE, 2015;10(10):e0140292.

How to Create an Organ-Specific Cancer Model

Organ Method Major CRO Original paper/Published review
Large intestine APC gene deletion The Jackson Laboratory A dominant mutation that predisposes to multiple intestinal neoplasia in the mouse
Science, 247(4940):322–324, 1990
Large intestine Azoxymethane injection + DSS Crown Bioscience / Charles River Laboratories / SMC Laboratories Dextran sodium sulfate strongly promotes colorectal carcinogenesis in ApcMin/+ mice: inflammatory stimuli by dextran sodium sulfate results in development of multiple colonic neoplasms
International Journal of Cancer, 118(1):25–34, 2006
Lung KrasGNDTransGenic The Jackson Laboratory Analysis of lung tumor initiation and progression using conditional expression of oncogenic K-ras
Genes & Development, 15(24):3243–3248, 2001
Liver Diethylnitrosamine injection SMC Laboratories Kinetics of diethylnitrosamine hepatocarcinogenesis in the infant mouse
Cancer Research, 43(9):4253–4259, 1983
Skin DMBA coating + TPA coating Charles River Laboratories, Inc. The role of croton oil applications associated with a single painting of a carcinogen in tumor induction of the mouse's skin
British Journal of Cancer, 1(4):383–391, 1947
Breast Polyoma middle T antigen The Jackson Laboratory Induction of mammary tumors by expression of polyomavirus middle T oncogene: a transgenic mouse model for metastatic disease
Molecular and Cellular Biology, 12(3):954–961, 1992
Prostate SV40 T antigen (prostate-specific) The Jackson Laboratory Prostate cancer in a transgenic mouse
Proceedings of the National Academy of Sciences USA, 92(8):3439–3443, 1995
Blood BCR-ABL fusion gene transfer Crown Bioscience Induction of chronic myelogenous leukemia in mice by the P210 bcr/abl gene of the Philadelphia chromosome
Science, 247(4944):824–830, 1990
Skin (Melanoma) B16 melanoma cell injection Crown Bioscience Biological behavior of malignant melanoma cells correlated to their survival in vivo
Cancer Research, 35(1):218–224, 1975
3 Recommended Contract Research Organizations for Non-Clinical Studies
— by Target goal and Expertise

In drug discovery, the quality and efficiency of non-clinical studies have a direct impact on clinical success rates, development costs, and overall length of time required in R&D. In recent years, there has been more demand for clinically relevant data, globally accepted reliability, and accurate early-stage screening. Thus, it is more important than ever to select the right CRO (Contract Research Organization) for strategic approach.
In this article, we highlight three CROs with proven technical capabilities, expertise, and long standing track records. These are our TOP 3 choices based on their capabilities and the specific target goals of the researchers for their non-clinical studies.

Pharmacology (Efficacy) Studies
Replicate unknown pathological models and
Discovery to clinically oriented drug evaluation
SMC Laboratories, Inc.
SMC Laboratories, Inc.
Reference: SMC Laboratories official website (https://www.smccro-lab.com/jp/)
  • SMC Laboratories has established a disease models using patented mouse technologies. The company has established proprietary pathological models—particularly in liver disease and fibrosis—and continues to expand their approach across a wide range of models in cancer, inflammation, and metabolic diseases.
  • From exploratory research to clinically oriented efficacy evaluation, SMC offers customized study designs, dosing strategies, and evaluation analysis tailored to each project. Their collaborative approachallows researchers to discuss and refine study plans together with SMC’s expert scientists.

  • With flexible small-scale study options and strong technical support, SMC Laboratories is an ideal partner for start-ups, biotech ventures, and academic institutions alike.
Safety Studies
Comprehensive Safety Evaluation for FIH Applications
labcorp
(Labcorp Drug Development)
labcorp
Reference: labcorp official website (https://jp.labcorp.com/)
  • labcorp provides a fully integrated GLP testing system aligned with international regulatory standards, including FDA, EMA, and PMDA requirements. All studies are conducted under ICH-compliant quality assurance, making it ready for data submission.
  • The company has extensive expertise in long-term toxicity studies such as Segment I–III reproductive and carcinogenicity studies, as well as 2-year chronic toxicity assessments.
  • labcorp’s comprehensive approach enables sponsors to efficiently outsource the entire preclinical package from toxicology, toxicokinetic (TK), and safety pharmacology study design to execution. This accelerates a path to First-in-Human (FIH) trials. For most of the global drug developers, this all-in-one service structure minimizes cost, risk, and expedite the time before advancing to clinical phase.
Pharmacokinetic (PK/PD) Studies
High-Precision Bioanalysis for Clinically Predictive PK/PD Evaluation
PhoenixBio
PhoenixBio
Source: PhoenixBio Official Website (https://phoenixbio.co.jp/)
  • PhoenixBio offers pharmacokinetic and hepatic metabolism studies using their proprietary PXB-mouse®, a humanized-liver chimeric mouse model. This platform enables the acquisition of data with high clinical correlation in ADME, drug–to-drug interaction studies, bridging the gap between preclinical and clinical stages.
  • With advanced LC-MS/MS-based bioanalysis, PhoenixBio provides aseamless workflow from plasma concentration measurement and metabolite identification to quantitative validation.

  • The company offersan integrated evaluation analysiscovering pharmacokinetics, hepatotoxicity, and safety with flexibility to accommodate complex modalities such as oligonucleotide and middle-molecule therapeutics. For compounds where hepatic metabolism is a development bottleneck—or where quantitative, reproducible exposure data are critical—PhoenixBio delivers unmatched analytical precision and consistency.

Consult Phoenix Bio for PK/PD analysis with a clinical focus