Antitumor efficacy
Single-agent, combination, and reference-arm efficacy studies using project-matched PDX cohorts.
PDX studies use patient-derived tumor tissue in immunodeficient mice for oncology efficacy, PK/PD, biomarker, and tissue-analysis work.
Tumor type, molecular context, cohort availability, host background, and study endpoints are aligned during technical review.
PDX models provide patient-derived tumor backgrounds for preclinical study design. Model selection is matched to the tumor context, compound mechanism, dosing strategy, and intended readouts.
Single-agent, combination, and reference-arm efficacy studies using project-matched PDX cohorts.
Exposure, target engagement, and efficacy correlation when PK/PD work is included in the protocol.
Model selection and downstream readouts aligned to relevant molecular or pathological features.
Tumor and protocol-defined tissue collection for histology, IHC, molecular, or other downstream analysis.
Endpoints are finalized with the selected model, species or strain, treatment design, and partner laboratory before study placement.
Tumor volume, tumor growth inhibition, regression, and response duration where included in the study design.
Body weight, clinical observations, and dosing tolerance.
Plasma, tumor, or selected tissue exposure where required.
Target engagement, IHC, pathway, molecular, or other fit-for-purpose readouts.
Final model, cohort, host background, study design, endpoints, timelines, and deliverables are confirmed during technical review.
Share the compound, mechanism, development question, preferred model, and intended endpoints. We can review fit, feasibility, and the appropriate partner-laboratory route for a PDX study.Required fields are marked with an asterisk(*).