Anti-clotting drug up for approval in US | Northern Rivers Health | Fitness and Medical News in Northern Rivers

Ricardo Alonso-Zaldivar | 8th January 2009

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IN what would be a scientific first, an anti-clotting drug made from the milk of genetically engineered goats moved closer to US government approval on Wednesday after experts at the Food and Drug Administration reported that the medication works and its safety is acceptable.

Called ATryn, and already approved for use in Europe, the drug is intended to help people with a rare hereditary disorder that makes them vulnerable to life-threatening blood clots.

Its approval in the US would be a major step toward new kinds of medications made not from chemicals, but from living organisms genetically manipulated by scientists. Similar drugs could be available in the next few years for a range of human ailments, including haemophilia.

ATryn was developed by a biotechnology company GTC Biotherapeutics by altering the genes of goats so they would produce milk rich in antithrombin, a protein that in humans acts as a natural blood thinner.

About 1 in 5,000 Americans do not produce enough of the protein, putting them at risk of developing blood clots in their veins. Such clots can be extremely painful.

If they break loose and travel through the bloodstream to the lungs or the brain, the consequences can be catastrophic. Pregnant women with the disorder are at high risk of miscarriage or stillbirth, because of blood clots in the placenta.

In their everyday lives, patients with the disorder are managed with conventional blood thinners. That would not change. ATryn is for use only when patients are undergoing surgery or having a baby, times when the risk of dangerous clots is particularly high.

Those patients would receive the drug by intravenous infusion for a limited time before and after their procedures.

Scientific advisers to the FDA will weigh the risks and benefits of the drug at a meeting on Friday and make a recommendation on approval. The FDA will make the final decision.

"It's the first time we've held an advisery committee meeting on any product from a genetically engineered animal," said FDA spokeswoman Siobhan DeLancey. If ATryn is approved, the FDA may require follow-up monitoring to make sure that patients' immune systems don't start making antibodies in reaction to the medication.

"I think this is an important tipping point," said Geoffrey Cox, chairman of GTC, the drug maker. "The real dramatic thing that is happening here is that we've been able to reduce some very clever science to the practical level of producing a drug that's safe and efficacious. Those things aren't trivial."

To make the drug, scientists at GTC put DNA for the human antithrombin protein into single cell embryos of goats. Goat embryos with the gene were then inserted into the wombs of surrogate mothers who gave birth to baby goats carrying the new trait.

The first of these goats were called the "founders." Their offspring also carry the gene. The females produce high levels of antithrombin in their milk, from which the protein is collected and purified.

GTC's production comes from a herd of about 200 goats on a farm in central Massachusetts, milked twice a day. "If you saw these animals, you wouldn't be able to tell any difference between them and any other goat," said Cox.

Up to now, antithrombin has been produced from blood products collected from human donors. Making the protein from goats may be better for humans, said Dr Stephan Moll, a haematologist at the University of North Carolina, Chapel Hill, who consults for the company. It would ensure a steady supply and reduce concerns about infection.

"It's a new mechanism by which drugs could be produced in pretty large volume in the future," said Moll, who is also a top medical adviser to the National Alliance for Thrombosis and Thrombofilia, a group that represents patients with the blood disorder.

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