Four Biotech Ideas With Legs to Run

Streetwise is a member of The Motley Fool Blog Network -- entries represent the personal opinion of the blogger and are not formally edited.

By George S. Mack, The Life Sciences Report

For more interviews with sector experts and analysts, please sign up for our newsletter at www.thelifesciencesreport.com.

I had an opportunity to ask George Zavoico a few questions for The Life Sciences Report. Zavoico is senior biotechnology analyst at the boutique investment bank, MLV & Co. He originally got his career underway as a research scientist and worked in big pharma at Bristol-Myers Squibb, as well as small biotech firms Alexion Pharmaceuticals and T Cell Sciences (now Celldex Therapeutics). Zavoico is a guy loaded with knowledge about molecular biology, drug development and the needs of patients, and this was a great opportunity for me to get a few haunting esoteric questions off my mind.

The first thing on my mind was to find out if there is still more room for new cholesterol drugs in the marketplace. Specifically I wanted to know if Resverlogix Corp.’s (TSX: RVX) (Zavoico: Buy; Target CA$6.50) RVX-208 could make a dent. “There is a very large potential market in this space,” he says, “Despite the continuing widespread use of statins, which explains the high level of interest. Even with improved control over cholesterol levels with statins, many people still suffer or die from acute coronary events or strokes.” He is particularly positive about the product’s “unique mechanism of action” which makes it so interesting. He points out the fact that there have been “notable failures” in attempts to raise high density lipoprotein (HDL), the “good” cholesterol (HDL-C), and he references recent data from Resverlogix’s phase 2b SUSTAIN trial that RVX-208 “significantly” raised levels of both HDL-C and Apo A-1, the latter of which is an important constituent of HDL-C and which helps to move cholesterol from vessels. “That’s why RVX-208 is starting to get noticed,” he says.

Zavoico follows BioCryst Pharmaceuticals Inc. (NASDAQ: BCRX) (Zavoico: Buy; Target $9), and out of curiosity I wanted to know about a preclinical compound, which is not something investors usually have much interest in because they rarely add value to shares.  This case could be different. The compound is BCX5191 for hepatitis C (HCV), which is a nucleoside, not a nucleotide. “The fact that BCX5191 is a nucleoside could be an important advantage,” says Zavoico. “It is not a prodrug (an inactive chemical that is subsequently activated in the body by normal metabolic processes), as are the nucleotides, and it has shown high potency, as well as no notable toxicity, in preclinical studies.” BioCryst says that a phase 1 trial is expected to start before year end. “It is a new approach in this space,” he says. “But as far as monetizing this asset, I think it is too early right now.” True, the main value driver for the company today is its phase 2, ready for phase 3, compound ulodesine, a purine nucleoside phosphorylase (PNP) inhibitor, which is being studied in gout. “We expect BioCryst to announce a partnership deal for this asset long before it does so with BCX5191,” he says.

Spectrum Pharmaceuticals Inc. (NASDAQ: SPPI) (Zavoico: Buy; Target $28) recently acquired Allos Therapeutics Inc. (NASDAQ: ALTH), with one marketed product, Folotyn (pralatrexate), which generated $50.5 million in net sales last year. The price tag for Allos was $206 million. Is the new business a value driver for Spectrum? “I believe it is,” says Zavoico. Folotyn is approved for treatment of relapsed or refractory peripheral T-cell lymphoma (PTCL). “We think the company can integrate Folotyn sales and marketing within its existing infrastructure for Fusilev (levoleucovorin) and Zevalin (ibritumomab tiuxetan) at minimal cost,” he says.

Threshold Pharmaceuticals (NASDAQ: THLD) (Zavoico: Buy; Target $14.50) delivered some exciting data from its phase 2b study of TH-302 in pancreatic cancer back in February. Given that news, is there any possibility that an early approval could be in the cards? “Definitely,” he says, “But not based on the phase 2b trial by itself since it was not set up as a pivotal trial since overall survival was a secondary endpoint. I envision a phase 3 trial of similar design, and most likely involving one of the two TH-302 doses evaluated in the phase 2b. If you've got success in phase 2b, typically there is no reason to make big changes to the trial design.” Before year end Zavoico expects Threshold to deliver some overall survival data in pancreatic cancer from its phase 2 study of TH-302 plus gemcitabine.

 

To read the entire interview with George Zavoico, visit www.thelifesciencesreport.com.

 

DISCLOSURE:
1) George S. Mack personally and/or his family own shares of the following companies mentioned in this interview: None


StreetWiseReport has no positions in the stocks mentioned above. The Motley Fool has no positions in the stocks mentioned above. Try any of our Foolish newsletter services free for 30 days. We Fools may not all hold the same opinions, but we all believe that considering a diverse range of insights makes us better investors. The Motley Fool has a disclosure policy.If you have questions about this post or the Fool’s blog network, click here for information.

From time to time, Streetwise Reports LLC and its directors, officers, employees or members of their families, as well as persons interviewed for articles on the site, may have a long or short position in securities mentioned and may make purchases and/or sales of those securities in the open market or otherwise. Streetwise Reports does not accept stock in exchange for services or render general or specific investment advice and do not endorse or recommend the business, products, services or securities of any industry or company mentioned in this report. Streetwise Reports LLC does not guarantee the accuracy or thoroughness of the information reported.

blog comments powered by Disqus