It is easy for biotech investors to get antsy when it comes to approvals from the Food and Drug Administration. The odds are so heavily stacked against each drug candidate that successful phase 3 trial results are often accompanied by a big sigh of relief. Investors might think: “The therapy worked as planned, now all the FDA has to do is sign a few papers and we’re off!” Depending on the severity of safety concerns, that’s generally the case.
Not so for sugammadex, a next-generation anesthesia reversal agent from Merck & Co., Inc. (NYSE:MRK), which failed to gain FDA approval in its first submission in early 2008. Rejection came despite getting the nod in Europe and gaining a unanimous approval recommendation from an FDA Advisory Committee. Although it’s not rare to see varying opinions on drugs between the FDA and its European counterpart, I’m not sure of any other examples that have taken more than five years to be resubmitted.
There’s a first time for everything, I guess, as the company is expecting a decision on the drug in the second half of this year. Why does it matter? Sugammadex (marketed as Bridion) had worldwide sales of only $261 million in 2012, but several analysts at JPMorgan have estimated that sales could grow to almost $1 billion in 2020 with FDA approval. That would offset a sizable chunk of falling sales from former megablockbuster Singulair.
How it works
If you undergo surgery, then chances are you’ll get a healthy dose of anesthesia. The drugs in general anesthesia do several things, the most important of which is inducing a neuromuscular blockade — or paralysis of your muscles. This is necessary in surgical applications for obvious reasons.
Equally important in a surgeon’s toolbox is the ability to reverse the neuromuscular blockade. The problem with current methods is twofold: (1) They are outdated and have not been improved much in the last several decades, and (2) they come with elevated cardiovascular risks (remember, your heart is a muscle). Sugammadex selectively binds to rocuronium, the main neuromuscular blocking agent in anesthesia, while sparing other enzymes related to nerve function. Therefore, it comes with improved cardiovascular stability.