Oncological clinical trials are usually longer and more complex than those targeting other diseases. We understand that a well-planned trial design and sound data analysis are the key to reliable clinical study results.

Our services include:

    • Scientific advice and support, eg. for new drug combinations
    • Design and clinical trial management
    • Evaluation of possible options for various indications
    • Clinical program review and “gap analysis”
    • Definition of intelligent trial endpoints
    • Statistical analysis plan and data programming
    • Definition of potential biomarkers
    • Close cooperation with cooperating partners
    • Involvement of international advisory board (optional)

CECOG Contact Information

Please feel free to contact us if you have any questions.