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While oncology remains the remains the most widely researched therapeutic area, clinical trials are complex and have consistently shown some of the lowest productivity rates over the last 10 years. Of many factors, the longer trial duration compared to other therapeutic areas, the significant number of patients and sites, the multiplicity of eligibility criteria, and the ever-increasing number of endpoints contribute particularly to the significant complexity of oncology clinical trials.

“Oncology clinical trials are particularly complex for patients and sites suffering from long study duration. Patient compliance can be affected by adverse events & perception of study burden over time, while protocols may be amended with additional visits, inclusion/exclusion criteria modification, or additional safety procedures.“

Dr. Frédéric Fiteni, oncology expert, Kayentis scientific advisory board.

At Kayentis, we have the necessary oncology experience to mitigate the specific challenges of complex oncology clinical trials. We support the development of your eCOA strategy to define relevant endpoints and focus on those that matter most to patients, allowing your research to improve both the health and quality of life of cancer patients.

Simplify your oncology clinical trial implementation with our scientific and operational eCOA advice

With extensive experience in oncology clinical trials, Kayentis offers strong support from the moment you start to design your trial.

Streamline your complex oncology clinical trials with our powerful solution

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