Pharmacodynamics (PD)

Advanced pharmacodynamic testing services for biomarker analysis, target engagement, and clinical trial support across all development phases.

Pharmacodynamics Services for Drug Development

Synexa provides comprehensive pharmacodynamics services to support drug development from preclinical through to late-phase clinical trials.

Our integrated approach combines advanced bioanalytical platforms, deep scientific expertise, and access to clinically relevant human samples, enabling robust assessment of drug mechanism, efficacy, and safety.

Laboratory technician using pipette equipment

Pharmacodynamic Applications

High Sensitivity

Mechanism of Action

Detailed characterisation of drug–target interactions, pathway modulation, and downstream biological effects.

Biomarker Discovery and Qualification

Identification and validation of PD biomarkers to support efficacy, safety, and patient stratification.

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Target Engagement and Receptor Occupancy

Quantitative assessment of drug binding and biological activity in blood and tissue samples.

GCLP-Compliant

Functional Ex Vivo Testing

Evaluation of drug efficacy and pathway inhibition, including immune activation and signalling pathways.

End-to-end Support

Longitudinal Monitoring

Real-time tracking of pharmacodynamic responses throughout clinical trials using multiplexed and systems-level approaches.

Sample types supported:

We support a diverse range of biologically relevant matrices, including:

  • Plasma and serum
  • Cerebrospinal fluid (CSF)
  • Urine
  • Tissue lysates
  • Cell and tissue culture supernatants
  • Minimally invasive matrices such as dried blood spots (DBS)

Pharmacodynamic Platforms

We leverage a broad suite of advanced platforms, including MSD, Olink, ELISA, Gyrolab, flow cytometry, LC‑MS/MS, and genomics and cellular assays, to deliver high-sensitivity, multi-dimensional pharmacodynamic insights.

Improving the quality of human health

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