ChemPartner PharmaTech Co., Ltd. is a CRO that provides a wide range of support from early drug discovery to non-clinical development, and this report examines and summarizes the company's features, disease models it possesses, case studies, and other information.
In addition to its headquarters in China, ChemPartner PharmaTech Co., Ltd. is based in San Francisco, USA,Strengths in chemistry, biology, pharmacology, DMPK (pharmacokinetics, metabolism), and exploratory toxicology and biologics discoveryWe are a global CRO (contract research organization) with
Along with providing services as a CRO, the company also serves as a partner to pharmaceutical and biotech companies to help them progress their projects. The company employs over 1,500 experienced scientists and pharmaceutical industry leaders educated in Europe and the United States to provide research and development services.
ChemPartner PharmaTech Co., Ltd.'s DMPK division has conducted over 80,000 ADME profiling and more than 50,000 exploratory toxicology studies since its establishment in 2007,Support drug discovery and development programs at partners worldwideThe company is a leading provider of services to the pharmacokinetic clientele. The company also provides services to pharmacokinetic clients.
The company has integrated DMPK/toxicity data to meet US FDA and NMPA regulatory requirements.IND application package providedWe are committed to Based on the hundreds of FDA filings we have handled, we provide strong support to our clients by preparing reports that meet the rigorous standards required by regulatory authorities (GLP/GCLP compliant ADMET packages).
The company offers a variety of in vivo disease models in the immunology and inflammation areas. For example, the company has developed theAdjuvant-induced arthritis (AIA) model in ratsThere is a In this model, female Lewis rats (weighing 180-200 g) are used to induce arthritis with CFA and to evaluate drug efficacy against human rheumatoid arthritis. In addition, BALB/c mice are used to evaluate inflammation and immune responseCon A-induced systemic inflammation modelWe also offer
This is a case study in which the company's antibody-drug conjugate (ADC), trastuzumab DM1 (T-DM1; a biosimilar of Cadusaila®), was synthesized and tested for in vitro efficacy in a xenograft model. In this case study,Study ADC formulation well tolerated at study dosesIt has been reported that
In addition to its Shanghai headquarters, ChemPartner PharmaTech Co., Ltd., based in San Francisco, provides a wide range of support services from early drug discovery to non-clinical development. One of our unique features is that we provide support for the preparation of IND application packages based on our extensive experience.
| Address | 1F & 3F, Block A, 2829 JinKe Road Zhangjiang Hi-Tech Park Pudong Shanghai, 201203, CN |
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| Tel | +86 21 5132 0088 |
| Website | https://chempartner.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.