Unlock The Full Potential Of Every Trial

Clinical trials are central to making scientific advancements for human health. They give hope to patients with serious illnesses, and they hold the promise of new breakthroughs in the treatment of disease. In turn, patients who participate in trials play a vital role in this critical process for developing and testing new therapies.

Despite serving as the gold standard of clinical evidence, clinical trial data contains only a slice of a trial participant’s health journey. This siloed data artificially limits the breadth of questions clinical researchers can answer. For example, clinical trial data is often inadequate to support explanation of adverse events, or super-responders and non-responders. Patients lost to follow-up are impossible to track, causing delays and risk of study failure. And the time and cost pressures of running trials can create too-short observation periods that preclude better understanding of the long-term impact on clinical outcomes.