This Biotech Company has the Potential to Hit the $100 Per Share Mark
By: Paul Tracy
Editor, StreetAuthority Market Advisor
Learn more about the Market Advisor (click here)
Published: December 4, 2007

Genentech (NYSE: DNA, $72.78) is a biotechnology company that focuses on treatments for serious and debilitating diseases such as cancer, rheumatoid arthritis and diseases of the immune system.

The company's major drugs include Rituxan, originally a treatment for lymphoma. Rituxan was also recently granted approval by the FDA for treatment of rheumatoid arthritis. Another key drug is Avastin, a treatment for some forms of lung and colon cancer. Genentech is also seeking to expand the list of diseases Avastin is approved for.

Competitive Advantages
The biotechnology industry has major barriers to entry. Genentech holds patents on the drug compounds it develops, and these patents legally shelter the firm from generic competition for many years. As the company is essentially a monopolist on these certain drugs, it can charge higher prices. And since many of its treatments are relatively new, Genentech has years of patent protection remaining on many drugs before it has to worry about competing generics.

Of course, it is possible for another company to develop a drug targeting the same diseases that Genentech does. However, that's less of a risk for DNA as it focuses on developing drugs for serious diseases where there are few existing treatments. As such, in many of its key markets Genentech has the only approved treatment.

In addition, markets like cancer drugs are considered critical by the FDA. The process to gain approval as a treatment for such serious diseases is far lower than for other conditions. While gaining FDA approval is never easy, DNA has fewer hurdles to cross than many other drug and biotech companies.

Growth Drivers
Genentech has two key growth drivers: the introduction of new drugs and expanded uses for existing drugs. To the first point, DNA has a sizeable pipeline of new drugs in development, including new treatments for rheumatoid arthritis, various forms of cancer and multiple sclerosis.

These drugs are in various phases of clinical trials. Many of them won't ever be approved by the FDA and research will be abandoned. But it would only take one treatment with the market potential of Avastin or Rituxan to generate growth for Genentech. The firm has a total of six compounds in the latter stages of clinical trials; these promising drugs could be approved for use over the next two to three years.

On a near-term basis, DNA has more potential to grow by expanding the use (or labeling) for existing treatments. Basically, the FDA approves new drugs for treatment of specific diseases in specific dosages. But some drugs work as a treatment for multiple conditions.

For example, the company's Avastin drug has already been approved for the treatment of certain types of colon and lung cancers. But now DNA is also applying for approval to use the same drug as a treatment against breast cancer, prostate cancer, lymphoma and other conditions. As drugs are approved to treat new diseases, the size of the company's addressable market grows. The company is seeking expanded labels for Herceptin, Rituxan and Tarceva, among other existing drugs.

Valuation and Outlook
DNA shares trade at around 21 times 2008 earnings. But with the company's long-term earnings growth rate standing at +23%, DNA has a PEG ratio of just 0.9.

Other large biotech companies like Amgen (Nasdaq: AMGN) trade at closer to 1.2 times their long-term growth rate. Given Genentech's better-than-average growth rate, my staff and I believe the stock should trade at a premium valuation to the rest of the group. Based on a PEG ratio of 1.2, shares of DNA could easily trade near $100 per share over the coming year.
 


Paul Tracy
Editor
StreetAuthority Market Advisor

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About Paul Tracy

Paul Tracy co-founded StreetAuthority.com and became the firm's Chief Investment Strategist in 2001. He also co-founded TopStockAnalysts.com in 2006. Prior to that he spent several years as Managing Editor at a multi-million dollar financial publishing firm with over 150,000 subscribers. In addition to his role as managing editor and lead financial writer, he was also responsible for equity research and managing a team of seasoned professional financial writers, researchers and market commentators.

Paul's previous experience includes a position at Robert W. Baird & Co.'s full-service brokerage operations as well as economic research work on a Money and Banking project funded by the National Bureau of Economic Research. He has also spent time doing outside consulting and research for the University of Virginia, has appeared as a guest expert on several prominent financial radio shows, and has been a featured speaker at various investment conferences across the U.S.

Paul graduated with a B.S. in Finance and Management from the McIntire School of Commerce at the University of Virginia.

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