New Hypertension Drug Wins FDA Approval

The US based drug manufacturers Gilead Sciences have won FDA approval for a new drug to treat a life-threatening lung disease. Key words: pulmonary arterial hypertension, liver injury, birth defect risks, death, heart failure, breath, rare disease, impotence pill, Viagra, endothelin, receptor, antagonists, relaxing, blood vessels, ambrisentan, Letairis. US-based biotechnology company Gilead Sciences said late Friday that the Food and Drug Administration (FDA) approved 5-milligram and 10-milligram tablets of its hypertension drug Letairis.

The drug, also called ambrisentan, is a once-daily treatment for pulmonary arterial hypertension.

Because of liver injury and birth defect risks, the drug will be available through the Letairis Education and Access Program, a restricted distribution program aimed at helping patients learn about the risks involved.

Pulmonary arterial hypertension is marked by extremely high blood pressure in the arteries that supply blood to the lungs. That makes it hard for people to breathe or exert themselves. It also puts a strain on the heart that eventually leads to heart failure and death. The disease affects about 100,000 Americans, according to the FDA.

It can cause severe shortness of breath and heart failure and, if untreated, leads to death in about three years, Gilead said.

The approval of Letairis is a big step in an effort by Gilead, one of the largest biotechnology companies, to diversify beyond its successful drugs for H.I.V. and AIDS into drugs for heart and lung diseases. Its AIDS drugs accounted for about 70 percent of its $3 billion in revenues last year.

Although pulmonary arterial hypertension is a fairly rare disease, there are already several treatments available for it, including Pfizer’s Revatio, which contains the same ingredient as its impotence pill, Viagra.

Gilead’s Letairis is likely to compete most directly against Tracleer, a drug sold by the Swiss-based Actelion. Both drugs are so-called endothelin receptor antagonists, which work by relaxing blood vessels. The drug Thelin, developed by the Houston-based Encysive, works the same way.

As it happened Encysive Pharmaceuticals learned yesterday that its drug would not be approved yet.

The F.D.A. had recommended instead another clinical trial to prove the drug’s efficacy.

This is the third time the F.D.A. has declined to give the go-ahead to Thelin, which is approved in Europe and Canada. Because of the multiple delays, Encysive lost a big lead over Gilead in the race for approval.

Gilead said its clinical trials showed that Letairis caused fewer cases of liver damage than Actelion’s drug. Nevertheless, the F.D.A., warning about liver damage and birth defects, is requiring Gilead to control carefully the distribution of the drug. Patients who use it are supposed to have blood tests for liver damage every month.

Gilead said Letairis, a once-a-day pill, will cost $3,940 a month, about the same as Tracleer, which is also known as bosentan. The company said it was establishing programs to help uninsured or underinsured patients obtain the drug.

The available drugs, including Letairis, can improve the ability of people to perform daily chores but do not restore normal health. In clinical trials Letairis improved the distance people could walk in six minutes by an average of 20 to 60 meters, or roughly 5 percent to 20 percent. The drug also slowed the disease.

The approval of Letairis was announced after the close of trading. Gilead’s shares rose 19 cents, to $80.83, in regular trading and then more than $1.50 after hours. Encysive shares fell 50 cents, to $4.10, in regular trading and another 25 cents after hours.

Source-Medindia
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