Small-Cap Ideas with Double-Digit Growth Potential: Frederick "Rick" Wise                     TICKERS: ATRC, ISRG, STJ, SYK, UNIS, VOLC
                                            Source: George S. Mack of The Life Sciences Report  (4/5/12) 
            You can own large medtech and diversified medical supply companies for  low volatility and incremental upside in a trending economy (yawn. . .),  but small- and mid-cap companies offer the real double-digit growth  possibilities. In this exclusive interview with  The Life Sciences Report,  Analyst and Managing Director Frederick "Rick" Wise of Leerink Swann  shares small-cap ideas that could wake up investors' portfolios. 
                            Companies Mentioned:  AtriCure Inc.   -   Intuitive Surgical Inc.   -  St. Jude Medical Inc.   -  Stryker Corporation   -  Unilife Corporation   -  Volcano Corp.  
                            The Life Sciences Report: Back in early March you attended  the 2012 Society of American Gastrointestinal and Endoscopic Surgeons  (SAGES) meeting in San Diego. Were there topics or companies that the  physicians were especially interested in?
  Frederick Wise:  Whether in a consumer setting or a medical meeting, doctors are drawn to  what's new, just like consumers would be. Physicians want to see  innovative technologies and understand them. There is a competitive  element to it, and two of the biggest companies in the general surgery  space were there:  Covidien Ltd. (COV:NYSE ) and  Johnson & Johnson (JNJ:NYSE)  Ethicon Endo-Surgery. Both were displaying a number of new surgical  products. I would say that one of the most exciting innovations right  now in the medical technology space  is in robotics, and for that reason  there was a great deal of interest at SAGES in  Intuitive Surgical Inc. (ISRG:NASDAQ), which is in the earliest stages of taking its da Vinci robot into the field of general surgery. That's a hot topic for sure.
  TLSR:  You follow the large-cap diversified supply and device companies. Every  recession brings a shakeout that creates efficiencies in business. Have  you seen this occur? 
  FW: That is a crucial point when  thinking about this industry today. Virtually every large company I  follow has, in some way, shape or form, announced formal restructurings,  increases in efficiencies and headcount reduction. Many have combined  business units and are looking for efficiencies in terms of  manufacturing, distribution or sourcing among other factors. 
  TLSR:  When the economy and employment recover and when patients return for  the elective procedures they've been putting off, will these large  companies be better positioned than they were in the past?
  FW:  Yes, I think the large-cap mature companies are moving past many of the  obvious negatives and challenges, and are extremely well positioned to  show some positive sales and operating leverage as the global economy  gradually recovers. Most of these larger companies have market-leading  positions in their major markets. All of them are reshaping their  portfolios and focusing on more innovative, differentiated products and  markets with potentially better pricing, better demand and better  margins. We don't have to get back to 15% top-line growth to see  leveraged bottom-line growth. Maybe we can get to a point in the  recovery where incremental top-line growth of even 12% could produce  very positive, very leveraged impacts on the bottom line.
  TLSR:  With a few exceptions you're basically in the large-cap medical device  and diversified supply space. What case do you make for them?
  FW:  I've never been very fond of generalizing, but I think you have to  start from the point that this group has underperformed the broader  markets and often the rest of healthcare now for several years.  Multiples are low; dividend yields have risen; free cash flow yields are  actually at historically high levels. This is all understandable in the  context of a maturing industry. I'm inclined to think that in a stable  to improving economy, with procedures rebounding, tremendous cash flows,  the improved operating leverage I mentioned, and with virtually all  large-cap companies increasing dividend payouts, that these could be  very attractive total return stories without a lot of risk over the next  few years.
  TLSR: Clearly, recurring revenue is part of the story for the mega-caps like Johnson & Johnson (J&J),  Abbott Laboratories (ABT:NYSE) and even smaller large caps like  Baxter International Inc. (BAX:NYSE)  and Covidien. But these companies are so widely diversified in their  product portfolios that growth is difficult. Also, huge market caps like  $90 billion (B) are hard to double. What kind of edge can investors  get?
  FW: I don't know that there is an edge so to speak,  but again, I don't think you have a lot of downside with the large-caps  mega companies like J&J, with revenues approaching $70B, and Abbott,  approaching $40B. My theme has been to focus on the relatively smaller  large-cap companies. In particular, I'm thinking of  St. Jude Medical Inc. (STJ:NYSE) and  Stryker Corporation (SYK:NYSE)  (now followed by another Leerink colleague),  both of which have a  relatively smaller revenue bases that should be growable, especially  given their increasingly attractive portfolios—especially if the  business has been run well and if their pipelines are growing and  expanding. That happens to be the case with both of these companies.
  TLSR: Speaking now to the mid-cap and small-cap companies in your coverage, is consolidation part of your theme?
  FW:  As I said, one of my themes is the low-risk, total-return concept. A  second theme is buying the larger-cap companies with the best pipelines,  but with a relatively small revenue basis and that are able to grow  faster than the group average—like St. Jude Medical and Stryker. My last  major theme is in the direction you suggest: consolidation.
  TLSR: May we speak about some of your recommendations for investors? Let's talk about specific companies. 
  FW:  I'm going to start with two companies I just initiated coverage on that  I'm very excited about. These are at the opposite end of the spectrum  from J&J, Abbott,  Medtronic Inc. (MDT:NYSE),  Boston Scientific Corp.  (BSX:NYSE) and St. Jude. 
  First, I would like to mention  AtriCure Inc. (ATRC:NASDAQ), the market leader in the surgical treatment of atrial fibrillation (AF), with roughly half of the surgical AF market. 
  TLSR: We're talking about atrial ablation, correct?
  FW:  Right, but ablation in a surgical setting. Atrial fibrillation, as you  know, is a complex and very serious disease. The idea is that you burn  lines in the heart tissue to stop the cascade of heart cell  contractions, which is a harmful process that almost is like dominos  falling, but in a chaotic fashion. With these burn lines, or lines of  block, you prevent the electrical arrhythmias from running all over the  heart, and if you are successful, you force them back into more regular  patterns. Electrophysiologists do atrial ablation procedures as a  catheter-based procedure from inside the heart. But, cardiac surgeons  have a major opportunity to treat AF from outside the heart. And if  you're doing coronary artery bypass graft (CABG) or valve replacement or  repair procedures, with the chest open, you've got open access to treat  the AF.
  TLSR: What's the size of this market?
  FW:  In the U.S. alone, again just looking at the AF procedures done  surgically, atrial ablation done with open-heart procedures could easily  be a $250 million (M) market. In round numbers, there are about 350,000  (350K) CABGs done annually in the United States alone, and obviously a  lot more internationally. Probably a quarter of them—or about 85K—are  performed on patients who have AF, which is not surprising since older  people, ages 60–80, tend to have multiple co-morbidities, multiple  clinical issues. Of the 85K potential cases of AF, fewer than 20% of  them are actually treated during a surgical procedure, despite the fact  that it's very well documented in clinical studies that approximately  80–90% of these patients are cured if their AF is treated during  surgery. Patients can even stop taking anticoagulants, which are  expensive and produce complicating side effects that make it difficult  for physicians to manage other co-morbidities. This is a great  procedure.
  TLSR: Rick, in December Atricure received FDA  approval for an expanded AF indication for its Isolator Synergy Surgical  Ablation system. You have written that this should drive growth, but  the stock didn't react particularly favorably, or for that matter  unfavorably.
  FW: I'm glad you asked about that because  it's important to reflect on the challenges AtriCure faces, as well as  the opportunities. Historically, for a couple of reasons, the company  was not able to optimally train and educate doctors about its atrial  fibrillation treatment. Cardiac surgeons got excited about this approach  to AF in the days before AtriCure became public in August 2005. Then  the company faced a very challenging period from 2008 to 2010, when the  Department of Justice (DOJ) and the U.S. Food and Drug Administration  (FDA) stepped up enforcement on off-label promotion of medical products  and drugs for all healthcare companies. Unfortunately, AtriCure was one  of the first companies to feel the ramifications of this stepped-up  enforcement. They weren't doing anything terrible, and their products  were approved, but approved for general approaches to cardiac ablating  procedures, rather than for specific targeted procedures, and not  specifically for atrial fibrillation use. And so again the FDA decided  to raise the bar, not just for AtriCure, but for everybody. We've also  seen this same raising of the regulatory bar in the spine/orthopedic arm  of the industry, for example. For Atricure, this process understandably  changed the company's approach to training and education. The very good  news for the company is that this DOJ investigation was fully resolved  in 2010. Having been the first in, if you will, AtriCure is also now, in  a sense, the first out. Now Atricure is the only company with an AF  device specifically approved and labeled for educating and training  doctors in atrial ablation, etc.
  Having said all that, frankly, I  can understand why investors are in a "show me" mode relative to the  stock. Especially since I'm in that mode, too. But I believe the company  is well positioned to show me—and show the rest of the investment  community—that they have a real opportunity to drive surgical AF  procedure penetration. It's like baking a cake in a way. If you have got  all the ingredients—flour, sugar, butter, etc.—you can turn those  ingredients into something very special. Although it will take a few  quarters to see it show up in revenues, I think there's an above average  chance that we'll see all the ingredients coming together to bake up  something very tasty at AtriCure.
  TLSR: Training is a  major issue. It's important to get new modalities into teaching  institutions because established clinicians do not want to take up new  procedures. The cardiovascular surgeon wants to graft the new vessels  onto the myocardium and get out.
  FW: Well said and so  true. As in the evolution of all procedures and all technologies, the  docs are thinking about what they know from three, five or eight years  ago, about earlier generations of these AF products and earlier  experiences with less-evolved products and techniques. In the case of  surgical atrial ablation, my due diligence suggests that under the best  circumstances it can take only an additional five minutes of operating  room time to do this procedure successfully. AtriCure's challenge is to  bring that message more clearly, succinctly and directly to surgeons,  and to help them understand what's possible despite their existing  mindsets. This is trench warfare for Atricure—doctor by doctor, hospital  by hospital. You can't just put an ad on the screen at the Super Bowl  to make this process happen. It’s a doc-by-doc training and education  process.
  TLSR: What was the other company you just initiated coverage on?
  FW: The other small-cap company is  Unilife Corporation (UNIS:NASDAQ).  It's more of a hospital supply-type name, but a very special one.  Unilife  manufactures prefilled syringes for large pharmaceutical and  biotech companies that want to take both new pipeline products, as well  as products coming off patent, and package them attractively in a  user-friendly, safer way—and in the process meaningfully differentiate  their delivery system from others. There's also the important and  essential issue of preventing accidental needle sticks for health care  workers and patients alike. The company has something like 12 issued  patents on their safety and delivery technologies, with a core patent  covering the key feature in all of Unilife's safety syringes, revolving  around the method of needle retraction within an integrated device.
  TLSR:  Rick, because these are off-patent drugs and because only a device as  been added, can these syringes be approved through the 510(k) process?
  FW:  The simple answer is yes, but your premise isn't 100% correct. Some are  going to be drugs coming off patent, absolutely. But some are going to  be drugs in development that can go through all the clinical trials with  the Unilife device. Some devices will be approved as a 510(k), some  will be approved as part of a device/drug combination.
  TLSR:  Unilife is a small-cap company, and manufacturing prefilled syringes  sounds like a capital-intensive business. I'm curious to know about the  drug trials you just referenced. Are the pharma partners going to be  paying Unilife for these syringes during the trials? Is the company  capitalized well enough to withstand these costs?
  FW:  Excellent question, because the company has barely any revenue right  now. Unilife does have development/customization programs, and it does  get paid, but the business is capital-intensive to the extent that it  had to build a facility. You have to spend money on equipment to  manufacture prototype devices, and the company has done this. Will it  need additional capital going forward? The simple answer is probably  yes. The complex answer is that maybe it will depend on how the deals  are structured and how the cash flows are structured. 
  TLSR: What else are you talking to investors about currently, Rick?
  FW: On the smaller side we continue to like  Volcano Corp. (VOLC:NASDAQ).  Volcano sees itself today as a very high-level, precision guided  therapy company. Volcano already is the global market leader in  intravascular ultrasound (IVUS), as well as being one of two key players  in the rapidly growing fractional flow reserve (FFR) measurement  market. IVUS imaging is used inside the coronary artery before, during  and after procedures to better understand both the anatomy and the  nature of the blockages inside the artery during percutaneous coronary  intervention (PCI) (stent) procedures.
  Volcano has had an  excellent track record since it became public in 2006. The company has  steadily gained market share on a global basis and at the same time has  invested heavily in the future. Right now the company has a global  installed base of some 6,800 IVUS instruments alone in catheter labs  around the world. And at this point, particularly with its latest  generation platform, it has the opportunity to expand into other areas  of imaging.
  As I mentioned, right now both Volcano and St. Jude  Medical are benefiting from the very rapid growth and acceptance of  fractional flow reserve (FFR) technology, another important diagnostic  tool for the catheter lab. It allows for very effective, very simple  assessment of coronary artery blockages. Bottom line, right up front  doctors get more accurate diagnoses and measurements to determine which  patients should get a stent, and whether patients should be stented at  all.
  TLSR: Is Volcano an acquisition candidate?
  FW:  I definitely believe Volcano is an acquisition candidate. As a  reminder, the other major player in the global IVUS market is Boston  Scientific.
  TLSR: Is Medtronic in this market?
  FW:  Medtronic does not offer either IVUS or FFR. Looking at the stent  market, Abbott, Boston Scientific, and Medtronic are the three major  players in the global stent market. But, of the three, only Boston has  IVUS, not FFR, and again, Volcano has both an IVUS and an FFR offering,  as well as a full pipeline of new additions to its precision guided  therapy portfolio.  So, you'd think that could be an interesting  portfolio addition at some point.
  TLSR: Do you also follow Boston Scientific?
  FW:  I think it's fair to say it is one of the most controversial large-cap  stocks I follow. Boston Scientific has had a very difficult decade. The  headwinds that the entire industry has been facing have been doubly or  triply challenging for Boston Scientific for a host of reasons. The  company very famously paid top dollar for Guidant in April 2006, just as  the implantable cardioverter defibrillator (ICD) market slowed  precipitously and just as the FDA was raising standards. Expenses were  too high and revenues were slowing in a world that was changing  dramatically, and the company suddenly found itself overleveraged. It  has taken the company time to adapt to the changing environment and its  changed circumstances—a process that is far along but still underway.
  TLSR: You've got Boston Scientific rated Outperform. Why?
  FW:  Today, with an entirely new management team in place and with  significant restructuring, the last of the major rating agencies has  just returned the company's debt to investment grade from a junk rating.  The company is generating over $1B/year free cash flow, and the  business has now stabilized. It has made significant and important  external investments in new and emerging markets, and in products. It  very recently made an acquisition that brought with it some  differentiated and potentially very exciting ICD technology. I think  Boston has positioned itself for much better revenue and  earnings-per-share growth over the next three to five years. Its stock  has understandably been largely avoided, but over the next one to two  years people are going to say, "Wow, that's better than I thought," as  opposed to the opposite.
  TLSR: You alluded to the recent  (March) deal to acquire Cameron Health, which has developed a "leadless"  ICD system. How important is a leadless system?
  FW: This  is a fascinating idea. Cameron has been working to develop this  technology over the last decade, and Boston has been an investor from  the beginning and has had an option to buy the company for a long time.  There were very specific milestones, and Cameron must have met those  milestones, based on the decision Boston has made to buy it.
  For  general background, you need to first appreciate that one of the major  challenges in using ICDs is that the leads create many complications.  Every major company has had performance challenges with their leads.  Having thin wires inside a beating heart for years can take a toll on  the products. With traditional ICDs, once the leads are in place they  grow into the heart tissue, and it's hard to take them out without a  very invasive procedure. If you could develop a product that, for a  significant number of patients, could eliminate the need for a lead, the  implantation procedure would be made simpler, faster, easier and less  complicated. Cameron has done that. Boston has acquired them, and I  think Boston could be well ahead of the pack in this respect.
  TLSR: At minimum, then, you are thinking Boston Scientific's cardiac rhythm management division could be revived?
  FW:  A fully approved Cameron device would be transformative to Boston's  cardiac rhythm management business. The ability to talk about a unique,  and potentially game-changing, technology with hospitals and physicians  would enhance Boston's ability to sustain and even gain both market  share and physicians' mind share. All this could be quite positive for  the company's Customer Relationship Management division outlook.
  TLSR: Rick, many thanks to you. I've enjoyed this.
  FW: Thank you. My pleasure. 
  Prior to joining Leerink Swann in 2008,   Frederick "Rick" Wise  was a senior managing director and medical supplies and devices analyst  with Bear Stearns for 22 years. For the past 13 years, he has been a  member of the Institutional Investor All-America Research Team, most  recently with a runner-up ranking in the 2009 poll.  He was also ranked  #4 in the 2006, 2007, and 2008 Greenwich Associates U.S. Equity Analysts  poll. Prior to joining Bear Stearns, Wise served as an analyst at  Kidder, Peabody & Co. and at Forbes, Inc. Wise received a master's  degree and a bachelor's degree from the Manhattan School of Music. He is  also a Chartered Financial Analyst.
  Want to read more exclusive Life Sciences Report interviews like this?  Sign up  for our free e-newsletter, and you'll learn when new articles have been  published. To see a list of recent interviews with industry analysts  and commentators, visit our  Exclusive Interviews page. |