A clinical trial heading for disaster is not for the faint of heart. Finding out late in the trial that requested data is not forthcoming, and the reasons for the delays are unclear, is a nightmare for any project manager and sponsor. When the drug indeed does look promising, how do you understand what’s going on and how do you get the sites, trial, and teams on the same page once more?
In order to put the trial back on track you need high impact diagnostic tools and a highly experienced clinical team familiar with the particular challenges to conduct the rescue and to implement the necessary changes with confidence.
The InterRx platform provides the flexibility to adapt to any FDA-approved protocol quickly in a matter of days and even permit autonomous transfer of previously collected data. Each data item can be autonomously reviewed for defect identification. Additionally, our InterRx TrialDiscovery study team has extensive experience with the analysis and change execution involved in a rescue trial.
With an experienced risk-management field team to precisely pinpoint where critical problems lie, rescue trials can be bolstered and completed in weeks and not years.