Axcelead Drug Discovery Partners, Inc. supports drug research and development. With in-house research facilities, the company provides a wide range of non-clinical studies in various areas, such as immunology, safety, and pharmacokinetics. Axcelead is also known for its ability to make precise, science-based proposals from the early stages of drug discovery with a clear focus on clinical development.
Axcelead offers packaged services for total support in non-clinical safety evaluation, including both GLP and non-GLP studies. The company provides integrated support toward IND submissions and out-licensing, working closely with its pharmacology and pharmacokinetics teams. This collaboration enables precise interpretation of safety margins, effective management of toxicity issues, and full assistance with regulatory submissions to PMDA or FDA.
Leveraging decades of drug discovery experience, Axcelead offers studies that optimize both cost and speed.
Axcelead’s consultants have deep understanding in pharmacology, synthesis, pharmacokinetics, and safety evaluation. They support the designing, execution, and analysis of non-clinical studies aligned with development strategies. They have knowledge and expertise from more than 100 IND applications and over 20 NDA submissions. The company’s strong partnerships with affiliated CROs also enable flexible and rapid trial management.
From early-stage research to pre-submission phase, Axcelead provides practical, hands-on support tailored to each client’s needs.
Axcelead has a dedicated pharmacokinetics department, which offers end-to-end PK (pharmacokinetics) and PD (pharmacodynamics) studies at the preclinical stage. Using both in vitro and in vivo studies, the company offers precise analyses of absorption, distribution, metabolism, and excretion (ADME) profiles.
Advanced technologies such as biomarker measurement, microtracer methods, and AMS (Accelerator Mass Spectrometry) can also be utilized to ensure a smooth transition from preclinical to clinical trials.
Axcelead has developed the “AXCC mouse,” an original model that exhibits pathology similar in patients with chronic kidney disease. This model carries the Col4a5 R471X mutation derived from Alport syndrome and shows albuminuria from 5 weeks of age, progressing through tubulointerstitial damage with fibrosis and decreased renal function, ultimately leading to renal failure.
Because this model can reliably detect drug efficacy against clinically used ARBs (angiotensin II receptor blockers) and reproduce disease pathology, it is often utilized for in vivo screening and biomarker discovery in chronic kidney disease research.
Reference URL:https://www.axcelead.com/author/sm_orderaxcelead-com/
In cancer immunology, Axcelead conducts preclinical studies with tumor immune profiling. By performing multifaceted analyses of immune cell spatial distribution and gene expression, the company can thoroughly evaluate the effects of drugs on the tumor microenvironment.
For example, by combining single-nucleus RNA sequencing and multiplex immunostaining techniques, Axcelead visualizes and quantifies immune responses—supporting the evaluation of therapeutic efficacy and safety.
Reference URL:https://www.axcelead.com/service/8226/?ref=sg
| Address | 2-26-1 Muraoka Higashi, Fujisawa City, Kanagawa Prefecture |
|---|---|
| Tel | Not listed on official website |
| Website | https://www.axcelead.com/ |
In non-clinical development, the choice of contract research organization shapes the quality of the data and the time it takes to reach the next decision. Below, three CROs are introduced by the type of study they support: pharmacology (efficacy) studies, safety studies, and pharmacokinetic (PK/PD) studies. Each summary describes the services the company offers so that you can match a provider to your target and development objective.
SMC Laboratories is a specialized non-clinical CRO focused on in vivo pharmacology and efficacy studies using disease-relevant animal models, particularly in fibrosis, inflammation, metabolic diseases, and oncology.
SMC Laboratories offers models covering the liver, lung, kidney, intestine, and oncology. Its portfolio includes the proprietary STAM™ model for MASH, fibrosis, and hepatocellular carcinoma.
Study plans are developed around the target biology, mechanism of action, disease stage, and development objective. Pharmacological endpoints can be combined with histopathology, biomarkers, and disease-specific readouts.
With experience from more than 1,000 studies for clients in 30 countries, SMC Laboratories supports programs from target validation and candidate selection through in vivo proof-of-concept studies.
Charles River provides non-clinical toxicology and safety assessment services for programs ranging from exploratory safety studies to IND-enabling development.
Services include single- and repeat-dose toxicology, dose-range finding, and general toxicology studies across multiple species and administration routes.
Charles River supports both non-GLP and GLP studies, allowing sponsors to progress from early safety characterization to studies intended for regulatory submissions.
Toxicology studies can be integrated with toxicokinetics, clinical pathology, histopathology, and safety pharmacology to support interpretation and IND-enabling safety packages.
Inotiv provides integrated PK/PD, DMPK, and bioanalytical services to characterize drug exposure and its relationship with pharmacological response.
PK studies characterize exposure, half-life, clearance, and other pharmacokinetic parameters needed to understand how a candidate behaves in the selected model.
Pharmacokinetic data can be combined with pharmacodynamic endpoints and bioanalysis to evaluate the relationship between drug exposure and pharmacological response.
Integrated DMPK, pharmacology, and safety information supports candidate comparison, dose selection, dosing-frequency optimization, and decisions about subsequent preclinical development.