At Cytoxis, we specialize in providing comprehensive consulting services to academic institutions, biotechnology firms, medical device companies, and pharmaceutical enterprises. In alignment with the transformation towards non-animal testing methodologies as recommend by FDA, Cytoxis is at the forefront of embracing innovative technologies to advance preclinical drug development while reducing reliance on traditional animal models.
Your project will be overseen by an experienced team responsible for planning, executing, and analyzing study outcomes. Through this collaboration, we strive to ensure that research findings are applicable to your R&D efforts and regulatory submissions, meeting the expectations of both internal and external stakeholders. Our clients are treated as partners, and our processes are designed to be flexible and adaptable, ensuring the timely delivery of high-quality results within budget constraints.
The journey of developing a new pharmaceutical drug is complex and time-consuming. It begins with the discovery of a promising compound, which then undergoes a rigorous process of selection and improvement to determine its suitability as a therapeutic treatment.
Through strategic partnerships with leading research institutes and contract research organizations, Cytoxis accesses a wide range of non-animal testing methods, such as advanced cell-based assays, patient-derived tissues, humanized technologies, and intricate computational modeling techniques.
At Cytoxis, we offer tailored solutions to address the unique needs and challenges of our clients in each stage of the pharmaceutical drug development process, from discovery to preclinical testing.
Harnessing the potential of biomarkers identified from patient samples, we pave the way for groundbreaking advancements in treatment strategies.
Utilizing cutting-edge cell-based assays, drug binding and biochemical assays, we conduct high-throughput screening and pathway analysis to evaluate selectivity and drug efficacy against target diseases.
We delve deep into drug absorption, distribution, metabolism, and excretion dynamics, paving the way for optimized pharmacokinetic profiles.
Employing sophisticated rodent models, including wild-type, transgenic and humanized models, we meticulously assess efficacy in complex physiological contexts, ensuring robust translational insights.
Employing a holistic approach encompassing both in vitro and in vivo methodologies, we meticulously evaluate the safety profile of candidate compounds and ensuring compliance with regulatory standards and safeguarding patient well-being.
Our network with diverse research institutions enables us to
customize each product and service program to meet your study requirements.
Cytoxis
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