Complex Clinical Trial Protocol Designs – Part II

Complex clinical trials can accelerate drug development, offering patients timely access to transformative therapies. At the same time, these studies can present challenges for trial management. Part I of this blog series explored data around complex studies plus various complex trial designs. Then, Part II addressed the site experience and the importance of having a […]

Protecting Patients, Protecting Your Study: The Benefits Of A Well-Run Data Monitoring Committee

Everything rests on having the right Data Monitoring Committee (DMC) in place. A well-run DMC protects patient safety and ensures data integrity. A poorly run one puts patients—and the trial itself—at risk. DMCs are independent groups of experts, typically clinicians and statisticians, who monitor patient safety and sometimes treatment efficacy data during a clinical trial. […]

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