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Amylin, Alkermes Long-Acting Diabetes Drug Wins FDA Approval on Third Try

By Molly Peterson
January 27, 2012 5:26 PM EST

Amylin Pharmaceuticals Inc. (AMLN) and Alkermes Plc (ALKS) succeeded in their third attempt to gain U.S. clearance for Bydureon, a once-weekly version of Amylin’s diabetes shot.

The Food and Drug Administration approved the drug for adults with Type 2 diabetes, the agency said today in a letter posted on their website.

Bydureon is a long-acting form of Byetta, a twice-daily injection that San Diego-based Amylin developed with Eli Lilly & Co. in a partnership that ended last year. Amylin lost almost half its market value on Oct. 20, 2010, after the FDA rejected Bydureon for a second time and sought a study on cardiac effects. The companies refiled for approval last year after the trial didn’t tie the drug to dangerous heart-rhythm changes.

“Bydureon is now the first and only weekly diabetes therapy approved in the United States,” Amylin Chief Executive Officer Daniel Bradbury said today on a conference call. The drug will be available in pharmacies next month, he said.

Amylin rose 15 percent to $14 in extended trading at 5:11 p.m. New York time. Alkermes, based in Dublin, gained 4.7 percent to $20. Trading on both companies was halted earlier pending the FDA’s announcement.

Amylin must complete a post-marketing clinical trial by 2018 to determine whether the treatment increases diabetes patients’ cardiovascular risks, the FDA said in the letter.

‘Execution Risk’

Bydureon’s U.S. revenue may surpass $1 billion in 2015, said Robyn Karnauskas, an analyst with Deutsche Bank in New York. Alkermes has said it will receive 8 percent of the drug’s net sales.

“We remain positive on Bydureon but significant execution risk remains,” Karnauskas, who has a “hold” rating on Amylin shares, said Jan. 24 in a note to investors. “We view Amylin’s capital structure as poor, with $2 billion of debt and $210 million in cash. However, more attractive financing options should open up” with FDA approval of the drug.

About 25.8 million people in the U.S. have diabetes, mostly the Type 2 form tied to being overweight and sedentary, according to the Centers for Disease Control and Prevention in Atlanta. The disease costs the nation an estimated $174 billion a year in medical expenses and lost productivity.

Diabetes is caused by an inability to use insulin to break down blood sugar into energy and can increase risks of heart disease, stroke and kidney damage. Medicines are used to reduce blood sugar.

Gila Monster

The active ingredient in Byetta and Bydureon, known as exenatide, stimulates pancreas cells to produce insulin when blood sugar is high. It is a synthetic version of a substance found in the saliva of the Gila monster. Bydureon uses technology developed by Alkermes to slowly release exenatide into the bloodstream with one dose a week. The drug won European Commission approval in June.

“Bydureon’s approval in the U.S. will not solve Amylin’s current issues,” said Michael King, an analyst at Rodman & Renshaw in New York who rates the shares “market underperform.”

Amylin took on a “tremendous financial burden” when it severed ties with Indianapolis-based Lilly and acquired the global marketing rights to exenatide for $1.45 billion, King said today in a note to investors. Amylin also faces competition from “established diabetes franchise players” including Bagsvaerd, Denmark-based Novo Nordisk A/S (NOVOB), he said.

Novo’s Victoza

Novo Nordisk, the world’s biggest insulin maker, sells Victoza, a once-daily shot that’s in the same medication class as exenatide. Victoza, cleared by the FDA in 2010, earned 2.32 billion kroner ($413 million) that year for the company.

While Bydureon’s weekly dosing may be more convenient for patients, its market potential may be hampered by data from a trial known as Duration-6 that found it didn’t work as well as Victoza, according to a Bloomberg Industries report.

Byetta, the twice-daily shot approved by the FDA in 2005, earned $559 million for Amylin and $151 million for Indianapolis-based Lilly in 2010, according to data compiled by Bloomberg. The two companies ended their decade-long partnership in November to resolve a legal dispute.

Amylin had sued in May to prevent Lilly from using the same sales force to market exenatide and linagliptin, a drug Lilly is developing with Boehringer Ingelheim GmbH (BING).

Revenue-Sharing

While Lilly won’t market Bydureon or Byetta in the U.S. under the deal that dissolved the partnership, the company will receive future revenue-sharing payments of as much as $1.2 billion from Amylin for both drugs. Amylin also agreed to make a one-time payment of $250 million to Lilly.

“With staggering debt, questionable execution skills, and the pincers of competition closing in, Amylin could soon be in a fight for its corporate life,” King said. “The only way out, in our view, is if the company quickly re-partners the exenatide franchise, a concept that is not entirely out of the question.”

Primary-care doctors may prefer Bydureon’s weekly dosing to diabetes drugs injected once or twice a day, said Ian Somaiya, an analyst with Piper Jaffray & Co. in New York.

“We believe the market continues to discount Bydureon’s approval and its billion-dollar market opportunity,” Somaiya said Jan. 25 in a note that recommended buying Amylin shares.

To contact the reporter on this story: Molly Peterson in Washington at mpeterson9@bloomberg.net

To contact the editor responsible for this story: Adriel Bettelheim at abettelheim@bloomberg.net.

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