Oncology: Preclinical, Clinical Trials & Post-Market

More than half a million people with cancer will die this year; our mission is to help you improve people's health and lives. From hundreds of preclinical pharmacology tumor models and cell line assays to running oncology clinical trials & post-market studies on thousands of patients in dozens of countries, we can help you get your next breakthrough cancer drug or precision medicine treatment to those who desperately need it.

Achieve that cancer breakthrough, improving health & lives. . .

Oncology has become the most research-intensive therapeutic area in drug development. You need a patient-centric CRO partner who can be wth you every step of the journey.

Embrace a personalized medicine approach that targets therapies to specific subsets of patients and begins in the preclinical phase of drug development
Utilize biomarkers in clinical oncology development to provide key data for earlier decision making as well as patient and site selection
Co-develop drug with an oncology companion diagnostics identifies to help identify patients most likely to benefit from your next cancer breakthrough

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Pediatrics Drug Development Solutions AND Oncology: Preclinical, Clinical and Post-Market Trials

Preclinical Oncology

Clinical Trials & Testing

Over 720 oncology trials (more than 100 immuno-oncology protocols in the past five years, performed in over 50 countries with nearly 20,000 patients.)
Data-driven and biomarker selection for patient recruitment

Oncology Diagnostics

Featured screening & diagnostic tests:

OmniSeq
IntelliGEN® Myeloid
PD-L1 Testing

Preclinical Oncology >

Clinical Oncology >

Oncology Diagnostics >

Preclinical Immunotherapy

The industry has approached immuno-oncology from many angles, thus requiring identification, development and refinement of models capable of recapitulating optimal biological dynamics along with the associated and relevant endpoints.

Precision Medicine & Clinical Trials

Making gains in precision medicine for clinical trials requires novel methods to quickly test and target the right therapy to the right individual. In addition to dozens of late-stage immuno-oncology clinical trials, we have also supported more than 70% of all FDA-approved companion diagnostic products.