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Janet Woodcock, MD, Director, CDER, FDA Bio and Contact Info
Listen (6:48) Is the FDA changing their approach?
Listen (4:34) Message to pharma: work together
Listen (5:08) How does a submission get breakthrough status?
Listen (2:29) It's a privilege to work somewhere you can really make a difference
Listen (2:47) What feedback lets you know you're doing a good job?
Recently named one of Fierce's 25 most influential people in biopharma, Janet Woodcock is changing things at the FDA. With her influential position as Director of CDER (Center for Drug Evaluation and Research) she is pushing for the use of more biomarkers and combination therapies. With targeted therapies, "it's easier to see that they work, and they require a smaller number of people in trials to demonstrate they're effective." This is not just talk from Woodcock. Last year the agency approved more drugs than in any of the previous 15 years. Woodcock speaks in the interview about her role as prod to the bio-pharma industry. She regularly urges them to work together and share more of their pre competitive work.
A couple weeks ago, Janet made headlines announcing the FDA's new "Breakthrough Status" program, a process for streamlining submissions with a special potential to make a big difference. In today's show, Janet explains what it take to get this designation, saying that potentially a drug could be approved after a Phase I trial. Woodcock has spent many years at the FDA and talks about the secrets to her success. "I have to use my own individual judgement about what is right for the people who are my customers, the patients."
Podcast brought to you by: Assay Depot - the world's largest cloud-based marketplace for research services. With Assay Depot, you can easily find the perfect research service provider and manage your project from anywhere in the world.
Marc Desgrousilliers, CTO, Clinovo Bio and Contact Info
Chapters: (Advance the marker)
1:26 Why does open source make sense for clinical trial software?
7:47 What are the objections to adopting open source?
11:12 Will adoption speed up clinical trials?
14:15 Is this the future?
18:16 Do FDA regulations pose special challenges?
22:04 BONUS: Swimming with sharks, literally
We've been tracking the open science movement here at Mendelspod with shows on open access publishing, platforms for collaboration and sharing data, and genome sharing for research. But what about open source software? Does this trend so strong in the IT world translate over to the life sciences. Marc Desgrousilliers, CTO of Clinovo says yes. Marc comes from the world of IT, spending several years at Microsoft where he led the development of Windows' network management. Marc is passionate about open source and the benefits that come from using software that is developed by the larger community. First of all the software has no licensing fees. (Clinovo makes their money on services that go along with the software.) Users are not dependent upon one software vendor. In addition, Marc points out, when software is designed by a large community free of charge, the user/designer volunteers tend to me very passionate about upgrades and development of the software. Are there special issues related to FDA regulation for open source software? Marc tells of his experience with the Clinovo software and of the validation they provide.
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Dr. Dave Albert, Founder, AliveCor Bio and Contact Info
Listen (8:43) Device cleared for medical community, not yet OTC
Listen (6:24) If I could, should I buy this device?
Listen (5:14) Fusing consumer health with traditional med device
Listen (5:09) Was this clearance a new exercise for the FDA?
Listen (4:40) How will you get around misaligned incentives for physicians?
Listen (1:49) Are there any downsides to piggy-backing on a smart phone?
Over the past year we've been closely following AliveCor, the new digital health pioneer. Cardiologist, David Albert, came up with a simple device that fits on the iPhone and can immediately give a person a readout of their ECG. His company, AliveCor, has generated a fair amount of buzz, not least of which is the notice they get from Steve Burrill in many of his talks. It's become a part of Steve's spiel about how healthcare is changing. Steve will stop, pull out his iPhone, put it on his chest and then watch the audience ooh and ah. The company has a stellar lineup of supporters/advisors. I mentioned Steve Burrill, who is an investor. Eric Topol, author of The Creative Destruction of Medicine, is a big fan.
Last week the company received the coveted FDA clearance to sell the device into the medical community. They'll now pursue an OTC clearance so that you and I could buy one for those scary days after a relationship break up or an earthquake and check our own heart stats. Is this company, a fusion of the new consumer health movement and traditional med device, an example of many companies to come? Dr Dave joins us to answer this question and others.
Mya Thomae, Founder and CEO, Myraqa Bio and Contact Info
Listen (9:22) What's least understood about the regulation of diagnostics?
Listen (2:22) How well is the FDA evolving from the old blockbuster drug model?
Listen (6:58) Regulatory advice fo diagnostics developers
Listen (9:32) How do you see the LDT issue playing out?
Listen (5:12) Are diagnostics way undervalued?
Listen (2:24) From music performance to regulatory affairs
Mya Thomae is an expert in the regulation of in vitro diagnostics. On today's show, she shares with us the advice that she gives her clients seeking FDA approval for their diagnostic products. Mya weighs in on the issue of LDTs: the FDA says it has the authority to regulate LDTs, but so far has issued no draft guidance. This is creating an unfair playing field for those producing CoDx, which are regulated. Has the FDA been waiting for the election to issue guidance? Does Obama's reelection or the recent 'Spygate' and meningitis outbreak really affect the FDA? Ms. Thomae travels often to Washington and offers her informed views.
Podcast brought to you by the upcoming Personalized Medicine World Conference taking place in Mountain View, CA, January 28-29. Over 100 speakers in three tracks will discuss how best to navigate the changing landscape of personalized medicine.
Walter Koch, PhD, Vice President, Head of Research, Roche Molecular Diagnostics Bio and Contact Info
Listen (4:07) Why hasn't the sequencing of the human genome led to more therapeutics?
Listen (8:48) Every drug in development at Roche has to have a biomarker strategy
Listen (4:53) Barriers to clinical adoption vary by disease area
Listen (6:33) Dealing with unlevel regulatory playing field for CoDx and LDTs
Listen (6:02) Whole genome tests and the FDA
Listen (2:32) Diagnostics undervalued
We often use the term 'big pharma.' Will we one day be writing about 'big diagnostics' as well? As part of our series Commercializing Diagnostics, we're joined by the head of global research at Roche Molecular Systems, Walter Koch. Walter joined Roche in 1998 when the first drafts of the human genome were coming out. In today's interview he admits to his naivety at the time the human genome sequence was completed about how soon we'd realize therapeutic results. Walter dives into Roche's drug development and companion diagnostic strategy and in the end looks forward to clinical genome sequencing. Walter was formerly at the FDA and puts in his two cents about how to deal with the unlevel playing field between the regulation of CoDx and LDTs.
Podcast brought to you by: Genia Technologies - Makers of integrated circuits for "Last Gen" DNA sequencing. Biology . . . meet the integrated circuit.
Deborah Kilpatrick, VP of Commercial, CardioDx Bio and Contact Info
Chapters: (Advance the marker)
0:40 Corus CAD™ - a diagnostic for a "huge cardiovascular market"
6:31 CardioDx - fusion between biotech, med device, high tech, and specialty pharma
10:11 The successful path toward reimbursement coverage
18:00 With Medicare approval and new funding, what is your focus now?
20:01 Diagnostics an answer to a troubled healthcare system
25:17 Selling to doctors with misaligned incentives
29:30 Personal journey from defense to diagnostics
Today we begin a series of shows about Commercializing Diagnostics. And we've chosen a company with some successes and great potential, CardioDx, based in Palo Alto, CA. They recently won Medicare coverage for their Corus CAD(™) test which can tell whether a blockage in your heart is causing symptoms such as chest pain or tiredness.
The challenge for diagnostic companies, according to Chief Commercial Officer, Deb Kilpatrick, is in demonstrating with data that the test is better than current methods. In this interview, Deb outlines the path that CardioDx took toward reimbursement and offers her insight for others pursuing what has become the holy grail for diagnostics companies. Indeed, there is now a conference devoted just to this issue of reimbursement. What next for CardioDx, we ask Deborah. This leads to a discussion about the role diagnostics companies can play in the challenges facing the healthcare system today. Will there be 'big diagnostics' along side 'big pharma?'
Don Jones, Vice President, Global Strategy and Market Development Qualcomm Life Bio and Contact Info
Listen (3:14) Why talk to Qualcomm on a life science media site?
Listen (2:32) What apps most excite you?
Listen (2:33) Consumers rather than patients
Listen (5:07) Qualcomm employee programs
Listen (5:44) Wireless can help us change our habits
Listen (1:34) Qualcomm as investor
Listen (1:54) The FDA challenge
Listen (3:45) Personal journey to wireless health
Listen (4:28) How do you currently interact with your doctor?
Every time you make a call on your cell phone, you’re using technology from Qualcomm. Now the chip maker is getting involved in healthcare. Don Jones, VP of global strategy and market development in wireless health, at Qualcomm is on a mission to bring wireless technologies to health and life sciences markets.
Jones was a founding board member of the West Wireless Health Institute, with Eric Topol and Gary and Mary West. It’s the world’s first and foremost Institute focused on the clinical efficacy and economic efficiencies of wireless technologies in healthcare. He founded Wireless Life Sciences Alliance, a local trade group based in San Diego.
Don shares his vision for where health is going in a world where more people have cell phones than have access to clean drinking water.
There has been a lot of whoop-ti-do about when the FDA will close enforcement discretion loopholes in regulations governing Laboratory Developed Tests. The FDA claims it has the authority, just hasn’t gotten around to rule making since 2006. CLIA and CAP regulations putatively cover these tests. Private health care payers and Medicare already reimburse for many of these tests under existing CPT codes.
Along with greater outcomes for patients, the movement now known as Personalized Medicine has also held great promise for new business.