A site where you can find recommended contractors for non-clinical testing|effical " Non-Clinical CROs and Agencies " Porsolt

Porsolt

Porsolt is a global CRO based in France.We provide a broad range of contract services for non-clinical development, ranging from early drug discovery screening to pharmacology, safety evaluation, pharmacokinetics, and support toward regulatory submissions.The tests are conducted not by an agency, but by our own research facility and specialized staff.

Characteristics of Porsolt's non-clinical contract testing services

Efficacy evaluation and pharmacological testing for diverse disease areas

In Porsolt,Central nervous system, cardiovascular, inflammation, oncology, pain, respiratory, liver disease, metabolic disease, skin disease, etc.We support non-clinical research across a wide range of fields. Equipped with various evaluation systems including in vitro, ex vivo, in ovo, and in vivo, we conduct pharmacological studies using multiple animal species. We can develop testing systems tailored to your research objectives, ranging from early-stage drug discovery screening to the efficacy evaluation of candidate compounds.

Safety pharmacology and non-clinical studies compliant with GLP

In the safety evaluation,Pharmacological and toxicological tests compliant with GLPare being conducted. We support studies evaluating effects on the cardiovascular, central nervous, and respiratory systems as a core battery based on ICH S7. A wide range of evaluations from in vitro to in vivo is possible, including hERG channel assays, blood pressure, heart rate, and electrocardiogram measurements, as well as respiratory function evaluations. Porsolt has continuously maintained its GLP compliance status since passing a GLP compliance audit in 2000.

Supporting drug discovery and development from pharmacokinetics to regulatory submissions

Not only efficacy evaluation,pharmacokinetic study, formulation analysis, bioanalysis, toxicity evaluationWe also offer services such as pharmacokinetics using multiple animal species including mice, rats, dogs, and minipigs, with the capability to collect samples of blood, plasma, cerebrospinal fluid, and various tissues. In addition, we provide scientific support for regulatory submissions at each stage of non-clinical development.

Source: Porsolt official website
https://www.porsolt.com/

An example of a disease model owned by Porsolt

At Porsolt, we have developed various in vivo and in vitro models for each disease area. For example, in the oncology field,orthotopic and subcutaneous xenograft models targeting breast cancer, lung cancer, colorectal cancer, glioblastoma, etc.Supports drug efficacy evaluation using [X]. Models can be selected according to the disease and evaluation purpose.

Source: Porsolt official website
https://www.porsolt.com/

Porsolt preclinical study cases

Predictive toxicity evaluation using 2D and 3D models

The Porsolt official website publishes papers and research results related to non-clinical research. For example,A study continuously evaluating drug withdrawal in rats using telemetryNow, we are measuring body temperature, amount of exercise, heart rate, mean arterial pressure, and other parameters over time. On the other hand, case studies summarizing the contents and results of trials commissioned by individual pharmaceutical companies are limited on our official website.

Source: Porsolt Official Document: In Vitro Predictive Toxicity Screening Assays during Early Stage Drug Development: Case Study Data for the Validity of 2D and 3D Models
https://www.porsolt.com/wp-content/uploads/2023/Catalog/catalog_interactive_Porsolt.pdf

Porsolt's corporate information

Source: Porsolt official website
https://www.porsolt.com/
AddressZ.A. de Glatigné, 53940 Le Genest-Saint-Isle, France
Tel+33 2 43 69 36 07
Websitehttps://www.porsolt.com/
By purpose and issue
Technical capabilities, expertise, and track recorda certain ...
Three recommendations for contract non-clinical testing services

In new drug development, the quality and efficiency of non-clinical studies directly affect clinical success rates, costs, and speed. Especially in recent years, there is a growing need for "highly extrapolatable data from humans," "reliability that can be used for international applications," and "accurate narrowing of focus in the early stages of drug discovery,Strategic thinking is also required in selecting a CRO (contract research organization).The company is now in a position to
In this article, we carefully select three companies that we recommend for each non-clinical purpose.

Pharmacology (Efficacy) Studies
Replicate unknown pathological models and
Discovery to clinically oriented drug evaluation
SMC Laboratories, Inc.
SMC Laboratories, Inc.
Reference: SMC Laboratories, Inc. official website (https://www.smccro-lab.com/jp/)
  • Reproduction and creation of unknown disease models in mice with patented technologyThe company is developing new disease models using mice. We are working on the development of new pathological models using mice, among others.Achievements in the area of liver disease and fibrosisLayers of
  • 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.

  • Small-lot production and technical consultation systemare in place and are easily accessible to venture and research organizations.
Toxicology Studies
Safety assessment for FIH application.
Can be handled in batches.
Labcorp Holdings Inc.
(Labcorp Drug Development)
Labcorp Holdings Inc.
Reference: Labcorp Holdings Inc. official website (https://jp.labcorp.com/)
  • FDA, EMA, PMDA, etc.GLP testing system in compliance with international regulationsThe system is fully equipped with a complete set of test methods, including the ICH-guideline-compliant data with reliability assurance, and can be designed with a view to submitting the data to the regulatory authorities in each country.
  • SEG I-III or 2-year toxicity, etc,Long-term studies including carcinogenicity and reproductive toxicityThe company has a high degree of expertise in this area.
  • Able to design and contract for bulk toxicology, TK, and safety pharmacology with a view to FIH.Efficient outsourcing of the entire non-clinical study up to the first human doseIt is possible to do so. For companies promoting global drug discovery, a system will be established to allow them to proceed while keeping costs and risks low.
Pharmacokinetic Studies(PK)
With high-precision bioanalysis
Clinically oriented PK/PD evaluation
PhoenixBio Co., Ltd.
PhoenixBio Co., Ltd.
Source: PhoenixBio Co., Ltd. Official Website (https://phoenixbio.co.jp/)
  • PXB mice® with human hepatocytes for pharmacokinetic and hepatic metabolism evaluation, including ADME and drug-drug interactions,Obtained highly extrapolative human dataPossible.
  • With advanced LC-MS/MS-based bioanalysis, PhoenixBio Co., Ltd. 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 Co., Ltd. delivers unmatched analytical precision and consistency.

By region
Disease animal model
ReviewList
Expertise & Track Record
3 Recommended Contract Non-Clinical Testing Services