Preclinical Study Services for Cardiovascular Drugs
Discovery & Development
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* Please note that all of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.

Preclinical Study Services for Cardiovascular Drugs

Inquiry

Preclinical evaluation of cardiovascular drugs plays an irreplaceable role in predicting potential drug toxicity prior to their first application to humans. Ace Therapeutics provides in vitro and in vivo preclinical studies of cardiovascular drugs to provide a theoretical basis for subsequent trials and clinical risk.


Overview of Drug Preclinical Research for Cardiovascular Drugs

In the development of new drugs for cardiovascular diseases, once a drug candidate has been identified, the next step is to conduct preclinical safety, pharmacokinetic, pharmacodynamic, and pharmacologically relevant studies to observe the biological activity of the compound in specific cardiovascular diseases and to assess the safety of the compound to support the initiation of clinical trials.

  • Pharmacokinetics/Pharmacodynamics (PK/PD)
    Understanding the absorption, distribution, metabolism, and excretion (ADME) of drugs in animals, these data can guide clinical studies to determine the form of administration as well as the frequency and dose of administration.
  • Safety Pharmacology
    In addition to demonstrating that the compound is biologically active against a specific target disease, there is a need to assess the effects of the drug beyond efficacy, such as possible side effects, especially on the cardiovascular, respiratory, and central nervous systems.
  • Toxicology
    Drug toxicity studies including acute toxicity, chronic toxicity, reproductive toxicity, carcinogenicity, and mutagenicity need to be completed before a new drug can enter clinical studies.

Overview of phase I and phase II drug-metabolismFig. 1 Overview of phase I and phase II drug-metabolism. (Smolders EJ, et al., 2019)

Our Services

Ace Therapeutics offers in vitro and in vivo preclinical study services for cardiovascular drugs, including preclinical pharmacodynamic studies, safety pharmacology studies, toxicology studies, and pharmacokinetic studies, which provide reference data and theoretical bases for subsequent clinical trials and clinical risks.

Preclinical Pharmacodynamic Study Services

We can provide customized preclinical drug pharmacology studies through our well-established pharmacology and efficacy research platforms.

Preclinical Pharmacokinetic Study Services

We can offer research services to obtain the basic metabolic kinetic parameters of drugs so as to elucidate the processes and characteristics of drug absorption, distribution, metabolism and excretion.

Preclinical Toxicology Study Services

We can provide our clients with various in vitro and in vivo toxicology studies to support toxicity data for the clinical submission of cardiovascular drugs.

Ace Therapeutics specializes in drug discovery and development for cardiovascular disease. With professional equipment platforms and dedicated research teams, we can provide preclinical research services for cardiovascular drugs according to the customized needs of our clients. If you are interested in our services, please don't hesitate to contact us.

Reference
  1. Smolders, E.J.; et al. Cardiovascular risk management and hepatitis C: Combining Drugs. Clin Pharmacokinet. 2019, 58(5): 565-592.
! All of our services and products are intended for preclinical research use only and cannot be intended for any clinical use.
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