大分子生物分析

Scientists working in a lab, with one focusing on a microscope and another analyzing data on a screen, highlighting research and innovation.

Pharmaron offers end-to-end pharmacokinetic (PK), pharmacodynamic (PD), and immunogenicity services for therapeutic biologic products. Our bioanalytical experts provide comprehensive study support, from lead identification to Phase IV clinical trials, with robust assay validations adhering to FDA/EMA/ICH regulatory standards.

Gloved hand of a scientist placing a vial into an automated laboratory machine, surrounded by various sample trays in a brightly lit lab.
Our Services

Biologics PK/PD

  • De novo development, transfer, and kit-based PK/PD assay support for preclinical and clinical programs
  • Assay development and validation for complex programs (e.g. Therapeutic proteins with endogenous counterparts)
  • Characterization of drug-dose response by quantitation of targets of interest
  • Supported Matrices:  Serum, plasma, urine, saliva, feces, bile, lymph, cerebrospinal fluid (CSF), tissue and cell lysates
Top-down view of an automated laboratory analyzer operated by a scientist in blue gloves, used for animal disease models and biomarker studies in immunology.
Our Services

Biomarker and Cytokine Analysis

  • Single and multi-plex assays available to best quantify early discovery, preclinical, and clinically meaningful targets for multiple therapeutic indications
  • Ability to initiate general screening against potential targets and take relevant biomarkers through preclinical and clinical studies (R&D, GLP, and GcLP)
  • Expertise in serum, plasma, PBMC, cell and tissue lysates with the ability to tailor requirements on a program-specific basis
Scientist is holding 96 well micro plate for ELISA immunoassay with pipettesScientist is putting reagents into 96 well micro plate including diluted proteins and sample with a single channel pipette for biological experiment
Our Services

Humoral Immune Response

  • Development and validation of Anti-drug Antibody (ADA) and Neutralizing Antibody (NAb) assays for pre-clinical and clinical studies tailored to regulatory needs (GLP, GcLP)
  • Utilization of cell-based transduction inhibition and plate-based ligand binding assays for inclusion/exclusion criteria and post-dose monitoring as a safety assessment
  • Regulatory and Industry-driven strategies for determining cutpoint in populations with pre-existing immunity to a therapeutic
  • Adherence to a multi-tiered approach per FDA Guidelines with further ADA characterization for isotyping, epitope specificity, and cross-reactivity
A gloved hand places a blood sample tube in a rack containing multiple vials, highlighting the preparation for immunogenicity assays.
Our Services

Cellular Immune Response

  • Establishment of Peripheral blood mononuclear cell (PBMC) assays to detect cellular responses against the test agent, detection of secreted immune molecules or proteins of interest (e.g., interleukins and cytokines)
  • Determination of appropriate PBMC preparations for analyzing antigen-specific cells
  • Optimized peptide pool concentrations for different assays