Experts in the complex world of clinical trial oncology response criteria implementation
Oncology clinical trials face new challenges with the continued advent of novel therapeutic areas in targeted cancer therapies and personalised immunotherapy. This increases the pressure to deliver precise tumor phenotyping, staging and early outcome predictors in trials. These are key areas where medical imaging is proving to be a critical component for the timely delivery of endpoints in oncology trials.
ICON has a highly experienced Oncology imaging service that is underpinned by a robust team of specialists that have more than 650 Oncology imaging trials under their wing, contributing to over 21 approvals by the FDA.
We work with thousands of sites across the globe to provide support, image quality assessments, reconciliation, and post processing.
Our team of highly trained specialists include key opinion leaders in radiology and clinical oncology, medical imaging experts, oncology study coordinators, biomedical engineers, statisticians, and allied support personnel.
Our specialists have vast experience with a wide variety of cancers, their treatments, and their image assessment criteria. They have mastered imaging technologies including CT, MRI, PET-CT, Nuclear Medicine, and Ultrasound which ensures your requirements are met for the successful completion of your trial.
- Indicationsinclude: Breast, Colorectal, Gastric, Glioblastoma, Glioma, Head and Neck, Lung, Lymphoma, Melanoma, Ovarian Prostate, Renal Cell
- Criteria include:RECIST, mRECIST, Choi, RANO, Cheson, Lugano Classification, Halleck, iRECIST, RECIL, iRANO/bmRANO/pedRANO, PCWG, PCWG3
Delivering benefits to your oncology study:
- Access to close to 700 highly trained radiologists
Wiith experience in body imaging, PET imaging and Nuclear medicine.
- Integrated clinical and medical imaging service teams
That have direct lines of communication, facilitating and streamlining project management. We prioritise study timelines across clinical and imaging services during start-up to minimise time to first patient in (FPI), and after last patient out (LPO) to reduce time to database lock.
- A range of support resources
Including in-house scientific experts, data management specialists, medical writing and translation services.
- High quality training support
Provided to the CTM/CRA team which assists with overall knowledge, timely submission of imaging, and the importance of open lines of communication with key site contacts.
- Greater accountability and collaboration
Across service teams for early identification and mitigation of study risks, lower query rates, and prompt implementation of any required corrective and preventative actions.
In this section
- Decentralised Clinical Trial Solutions
- Real World Intelligence
Cardiac Safety Monitoring
Clinical & Scientific Operations
- Clinical Operations
Clinical Supplies Management
- Clinical data science
Endpoint Adjudication Services
- Global Logistics
- Interactive Response Technology
- Investigator Payments
Medical Call Centre Services
Medical Writing & Publishing
Project and Program Management
Site Identification and Feasibility
- Early Clinical
- Language Services
- Medical Imaging
- Site & Patient Solutions
- Strategic Solutions
- Symphony Health
Decentralised Clinical Trial Solutions