TABLE 5.
What is a hypothesis that could be tested in an international collaboration and its ideal framework? |
Is there a way to develop common signatures that can track patients noninvasively across clinical studies/trial cohorts? |
Can harmonisation of available data in U-BIOPRED and SARP cohorts expose novel mechanisms or identify predictors of clinical response in subgroups of patients with asthma? |
Is the IL-6 signature identified in the U-BIOPRED cohort similar to SARP? |
Does the timing of data collection for clinical studies have an impact on clinical data collection and outcome measures such as IL-6 and other circulating mediators? |
How can timing factors related to the circadian rhythm be identified and managed for accuracy? |
U-BIOPRED: Unbiased Biomarkers for the Prediction of Respiratory Disease Outcomes; SARP: Severe Asthma Research Program; IL-6: interleukin-6.