GlaxoSmithKline plc (ADR) (GSK), Sanofi SA (ADR) (SNY), Theravance Inc (THRX): This Week in Biotech

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With the SPDR S&P Biotech Index up 38% over the trailing-12-month period, it’s evident that investment dollars are willingly flowing into the biotech sector. Keeping that in mind, let’s have a look at some of the rulings, studies, and companies that made waves in the sector last week.

With the American Society of Clinical Oncology’s annual meeting right around the corner, we were privy to plenty of clinical data (both good and bad), a three-month early drug approval from the Food and Drug Administration, and a head-scratcher of a deal in the biotech sector.

GlaxoSmithKline plc (ADR)Starting in reverse, Elan Corporation, plc (ADR) (NYSE:ELN) surprised investors on Monday by coming out of the bleachers and entering into a $1 billion royalty deal with Theravance Inc (NASDAQ:THRX). If you recall, Theravance Inc (NASDAQ:THRX) and development partner GlaxoSmithKline plc (ADR) (NYSE:GSK) received FDA approval for their long-acting COPD maintenance inhaled treatment Breo Ellipta last week. The companies are also working on Breo Anoro which is also under FDA review and two additional compounds. The deal by Elan Corporation, plc (ADR) (NYSE:ELN) entitles it to receive 21% of Theravance Inc (NASDAQ:THRX)’s royalties and assumes that the remainder of respiratory treatments will be quite successful. While a fantastic deal for Theravance Inc (NASDAQ:THRX) shareholders, it’s a hefty price to pay for Elan, which appears to be wildly reaching for growth ideas.

On the clinical data front, Sanofi SA (ADR) (NYSE:SNY) delivered positive news to investors on Friday with its JAK2 inhibitor SAR302503. The drug, which is meant to treat myelofibrosis, met its primary endpoint in late-stage trials of reducing spleen volume by greater than 35% after 24 weeks in both dosage groups. The side effects of SAR302503 were consistent with phase 1 trials, and Sanofi SA (ADR) (NYSE:SNY) could file for regulatory approval relatively soon.

Roche also reported positive initial data for its chronic lymphocytic leukemia drug, GA-101 (also known as obinutuzumab), on Thursday. When combined with chlorambucil, GA-101 demonstrated a statistically significant 86% reduction in disease progression, relapse, or death. Median progression-free survival also more than doubled to 23 months from just the 10.9 months associated with taking chlorambucil by itself. Roche noted that it will present its full data set on GA-101 at ASCO.

Things didn’t go nearly as well for Oncothyreon Inc (USA) (NASDAQ:ONTY), which announced the full, and disappointing, results from its unresectable, locally advanced non-small-cell lung cancer drug, L-BLP25. While delivering a median overall survival of 25.6 months, it wasn’t statistically significant next to the median OS of 22.3 months for the placebo group. Oncothyreon Inc (USA) (NASDAQ:ONTY) also revealed initial results from two mid-stage studies of PX-866 in patients with glioblastoma and castration-resistant prostate cancer. Both results proved decent, but not enough to excite investors would were disappointed by L-BLP25’s failure.

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