The recent collapse of Medtronic's clinical trial for a blood pressure treatment device marks another watershed as the era of dynamic growth through invention comes to a close in the medical device industry.
Yes, it's just one patient trial for one product. But it's not every day that doubts about whether a medical device actually works take a billion-dollar acquisition down more or less to zero.
Fridley-based Medtronic has been measured in what it has said, just that it stopped its large pivotal trial of its Symplicity HTN-3 renal denervation product because the results so far showed that it "failed to meet its primary efficacy endpoint," or wasn't effective enough at treating hypertension. Medtronic got the product in a 2011 acquisition of a start-up called Ardian, so it added that a write-down of the value of the related assets is "likely."
Medtronic is still selling the product for use in some countries and may yet get something more out of the deal. It's appointing a panel of experts to look over the trial, so it's possible that the panel will find flaws in the trial itself and Medtronic will try again.
In conversations with investors and device executives in the last week, however, no one sounded particularly optimistic that Medtronic had anything here but a complete bust.
And if this can happen to Medtronic, the old assumptions about acceptable risk in medical technology need to be reconsidered and the already long road from invention to product launch just got a whole lot longer.
Companies like Medtronic and St. Jude Medical have been calculated risk takers, and the risk they don't usually take is technical risk. The device has to work.
But there's also an important distinction to be made between technical risk and clinical risk, and it was clinical risk that derailed the Symplicity device. All indications are that the devices do zap the renal nerves as designed, but doing so did not show enough effect on patient blood pressure.