Highlights of the important and the interesting from the world of health care:
Tough times for biotech IPOs: The decision of Anthera Pharmaceuticals this week to delay its initial public offering signals rough going in the IPO market for biotech firms. Anthera’s underwriters declined to comment on the reason for decision, Reuters reports. But an analyst had a good idea why it happened: “Investors were likely concerned about Anthera’s inadequate funding, unclear timeline to commercialization and lack of collaboration agreements with larger pharmas.” Anthera’s postponement comes on the heels of an IPO by Ironwood Pharmaceuticals which netted the company far less than it had planned. Irownwood sought a price between $14 and $16 a share, but had to settle for $11.25.
A Deep-dive Into Specialty Pharma
A specialty drug is a class of prescription medications used to treat complex, chronic or rare medical conditions. Although this classification was originally intended to define the treatment of rare, also termed “orphan” diseases, affecting fewer than 200,000 people in the US, more recently, specialty drugs have emerged as the cornerstone of treatment for chronic and complex diseases such as cancer, autoimmune conditions, diabetes, hepatitis C, and HIV/AIDS.
Anthera’s postponement marks the seventh time a company has delayed an IPO this year. Worse, the 10 companies that have completed IPOs cut their prices by 30 percent on average, Bloomberg reports. To be clear, most of those companies weren’t biotechs. But the takeaway from recent events is that today’s market isn’t going to support the traditional biotech startup that has big dreams but no sales, FierceBiotech reports.
Investors are proving extremely hard-headed about the companies they back, and any biotech that isn’t counting revenue or at least close to an approval for a promising first-in-class therapy will find it very tough going – for now.
The FDA and EHRs–a match made in acronym heaven: Concerned about six deaths reportedly linked to electronic health records systems, the U.S. Food and Drug Administration is considering whether to bring health information technology under its regulatory purview, the Huffington Post reports. And those six deaths may be only “the tip of the iceberg,” an FDA official warns. The agency has received 260 reports of “adverse events” caused by health information technology over the last two years, and bear in mind that these are just voluntary reports so the numbers could be much higher.
The FDA says the adverse events generally had one of four causes: Errors involving the confusion of one patient’s records with another’s, or the mistaken combination of two patients’ medical files; the loss of information or the corruption of data; medication and/or dosing errors; and software incompatibility issues. For a rare and refreshing instance of a member of an industry actually welcoming regulation, and in turn unselfishly acknowledging the reality that regulation can actually be to the public’s benefit (even if it is to the industry’s detriment), I salute prominent tech blogger Health Care IT Guy:
Without stricter regulations like we have on medical devices, I’m afraid we won’t get the safety attention we need to bring to bear. Hospital IT systems can, do, and will kill when not used or implemented properly. It’s a shame that we need the government to improve quality but maybe just the fear of regulations can do the trick.
BioLabs Pegasus Park Cultivates Life Science Ecosystem
Gabby Everett, the site director for BioLabs Pegasus Park, offered a tour of the space and shared some examples of why early-stage life science companies should choose North Texas.
Stop pandering to your parties and start serving us. Stop jockeying for power and start fighting for what’s right. If you don’t, I think it’s just a matter of time before angry mobs with torches show up at your doorstep, before another shot is heard in a small town in Massachusetts and another revolution is joined.