DecisionView Looks to Help Speed Up Pharma’s Painfully Slow Trials

For years, real-time analytics have helped people to see patterns in data about traffic, weather, and the stock market. The pharmaceutical industry has plenty of ways it could benefit from real-time data feedback, and one of the obvious ones is in finding bottlenecks that slow down patient enrollment in the clinical trials that cost the industry $35 billion a year.

If a San Francisco-based software company called DecisionView is successful, it could end up teaching Big Pharma some powerful lessons about real-time data analytics, which could in turn enable drugmakers to get more of its studies done on time and budget.

DecisionView, a private software company with 40 employees, is releasing a new report on clinical trial enrollment patterns, based on a deep pool of data it has gathered on trials from top drugmakers like Merck, GlaxoSmithKline, and Roche. The report, which encompasses 730 trials conducted between 2005 and 2011, sums up data on patient enrollment at 35,000 clinical sites, across 14 different disease categories, in 85 countries.

There’s no single earth-shaking conclusion, CEO Linda Drumright says, but there are lots of fine-grained details for clinical trial planners to comb through. For example, when looking at Brazil, Russia, India and China, the analysis shows China enrolls significantly more patients per study, but takes the longest time to recruit. India and Brazil are the fastest at enrolling patients once studies are ongoing, in an average of 26 weeks. Trials get up and running the quickest in Russia (31 weeks on average), while Brazil takes the longest to get the trials started (55 weeks).

Linda Drumright, CEO of DecisionView

The report is intended to establish a benchmark that pharma companies can use to see how well they’re doing at organizing their own clinical trials. By drilling deeper into data on enrollment patterns of trials, site by site, disease by disease, and comparing each study’s performance to the data in the report, DecisionView is betting that pharma companies will be able to make mid-stream adjustments to trials that can keep studies from dragging on and wasting too much money. It’s a huge industry bugaboo, as an estimated 94 percent of industry-run trials finish behind schedule, and sponsors are said to lose an average of $8 million a day when a drug’s arrival on the market is delayed. Each year, about $35 billion is spent on clinical trials, and about 13,000 trials are enrolling in the U.S. at any given time, meaning there’s big business in helping things run more smoothly.

“It’s insufficient to make guesses when you are betting so much money,” Drumright says.

DecisionView, backed by Granite Ventures and Aeris Capital, has gradually built up some momentum for its offerings since it was founded in 2004. GlaxoSmithKline became its first major pharma customer in 2007. While DecisionView doesn’t disclose its annual revenues, Drumright says eight of the world’s top 10 pharma companies use its product, revenues have almost tripled since 2010, and the company expects to break even this year.

The idea at DecisionView is all about helping companies do a better job of planning the fastest, best possible trial of, say, a new rheumatoid arthritis drug at 100 sites around the world—and then make sure that such a train and all its moving parts remains on track. While there are companies out there with software designed to randomize patients in trials, or help manage data from clinical trials in an FDA-validated way, there wasn’t really a corporate software program specifically for getting patients enrolled on time, Drumright says. Companies were using Excel spreadsheets to track enrollment, or homebrewed software, and weren’t really getting real-time visibility into specific sites, regions, or countries, where enrollment had bogged down, she says.

To deal with that, the DecisionView program contains what

Author: Luke Timmerman

Luke is an award-winning journalist specializing in life sciences. He has served as national biotechnology editor for Xconomy and national biotechnology reporter for Bloomberg News. Luke got started covering life sciences at The Seattle Times, where he was the lead reporter on an investigation of doctors who leaked confidential information about clinical trials to investors. The story won the Scripps Howard National Journalism Award and several other national prizes. Luke holds a bachelor’s degree in journalism from the University of Wisconsin-Madison, and during the 2005-2006 academic year, he was a Knight Science Journalism Fellow at MIT.