Case Study
Creating an Innovative EDC Build Solution for Oncology Master Protocol Designs
PROJECT BACKGROUND With oncology research, the clock is always ticking. This is why many oncology clinical trials use master protocols and other innovative designs. These kinds of studies, such as basket and umbrella trials, look to speed therapy development by investigating as many hypotheses as possible, all at once, through multiple concurrent studies and sub-studies. This increases the complexity of the trials and requires a high degree of flexibility – to deal with the inevitable need for amendments.
COMPANY PROFILE ■ ■
Oncology-focused biopharmaceutical company Headquartered in United States
SERVICES UTILIZED ■ ■
Biometrics Services Clinical Data Acquisition
THE CHALLENGE A leading specialty biopharma company focused on developing innovative new oncology therapies planned several early phase clinical trials using complex designs including master protocol approaches. The company’s portfolio included trials with up to 12 study arms, some with over 15 patient cohorts. These study arms typically involve multiple external data sources and protocol amendments are common. Traditional EDC build approaches for these types of designs require a new casebook for each study part, a time-consuming and labor-intensive process
that creates an operationally inefficient EDC build, risks downstream complications when study arms are added or dropped, and incurs greater (up to 4x) software pass-through costs as well as overall services costs. The company needed a flexible electronic data capture (EDC) build solution that would allow them to collect the data from multiple study arms within complex master protocols in a more streamlined manner, avoiding time delays as compared with the traditional EDC approach, without the additional software costs.