The FDA emphasizes the importance of ECG evaluation early in development, stating:
"Drugs are expected to receive a clinical electrocardiographic evaluation beginning early in clinical development, typically including a single trial dedicated to evaluating their effect on cardiac repolarization ('thorough QT/QTc study')".
This regulatory perspective underscores the critical role of QT monitoring in ensuring drug safety.
The conventional reliance on 12-lead ECGs, while considered the gold standard for comprehensive cardiac monitoring, often necessitates on-site clinic visits. This imposes a logistical burden on patients and raises the risk of higher dropout rates and trial delays for sponsors. While indispensable for specific assessments, the routine use of these traditional methods can lead to unnecessary obstacles.
What if there was a way to supplement most trials with a solution that obtained all the essential cardiac data with far less burden?
This question is becoming increasingly relevant as the industry shifts towards more patient-centric trial designs, which drives broader adoption of digital health technologies. Significantly, portable 6-lead devices like the KardiaMobile® 6L are not just a future promise; they are reshaping cardiac monitoring in clinical trials today with their clinical utility, flexibility, and patient-centric design.