Wyeth Undergoes Revision As Teva Launches Generic Protonix

By Matthew Williams
19:03, December 24th 2007
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Wyeth Undergoes Revision As Teva Launches Generic Protonix

Wyeth announced on Monday that it would revise the business plan after rival Teva Pharmaceuticals Industries Ltd launched a drug similar to Protonix, Wyeath’s anti-acid medicine. Due to this fact Wyeth fell in the last four months in New York trading.

Wyeth said that it will sue the company, which is based in Israel, for its lost profits and damages, Reuters reports. The trial will begin in the second half of the next year.

Wyeth executives said that Teva will stop shipments for the drug for the next 30 days as the two companies will try to reach an agreement.

Meanwhile, Wyeath began to examine everything in the company in order to cut costs so as to prepare for the impact of Protonix’s generic launch, which triggered sales of about $1.4 billion in the first nine months of the year.

Bernard Poussot, Wyeth chief operating officer, said at a conference call: “We will look at every area of investing and spending.”

He also said that the company is thinking of making partnerships with other drug companies.

Today, at 10:57 a.m., Wyeth fell 3.6 percent, to $45.16 in New York Stock Exchange composite trading.

Petah Tikva, Israel-based Teva, the biggest producer of generic drugs, raised 3.7 percent, to $46.84, according to Bloomerg.com.

On September 6 a judge ruled that Teva can sell a low-cost version of Protonix before the latter expires in 2010.

For months the companies have tried to reach an agreement.

Poussot said to investigators: “It is impossible to ascertain exactly how much of Teva's product has entered or may enter the market. We continue to explore settlement possibilities but only if this makes sense for Wyeth and shareholders.”

Also today Wyeth announced that the U.S. Food and Drug Administration rejected for the second time its experimental medicine for the prevention of post-menopausal osteoporosis

FDA asked for more details about the drug, bazedoxifene, but according to Wyeth the agency wasn’t satisfied with the answers.

In a statement the company said: "The FDA has requested further analyses and discussion concerning the incidence of stroke and venous thrombotic events.”

 



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