Posts Tagged ‘FDA’

Antigen Express synthetic H1N1 flu vaccine in the works

Friday, September 25th, 2009

By Julie Donnelly

Julie Donnelly

Worcester-based synthetic vaccine company Antigen Express Inc. is hard at work making the next generation of vaccines against both avian and swine flu.

The company wasn’t among the five pharmaceutical giants to be approved to produce the H1N1 vaccine that will be distributed throughout the U.S. in the next few weeks. In fact, Antigen Express is still waiting for the FDA to approve protocols for clinical trials of its H1N1 vaccine — company President Eric von Hofe said he expects those conversations to happen in the next few weeks. Von Hofe said the company is currently doing trials in Lebanon and is seeking approval to do clinical trials from European Union regulators as well.

The FDA has never approved a synthetic vaccine for prophylactic use. But von Hofe said that he thinks the regulator is starting to warm up to the novel technology.

“Back when there was the H5N1 (avian flu) scare, the FDA was very skeptical of synthetic vaccines. But then they tried to make a vaccine out of eggs and they just couldn’t do it because it was so toxic. Now I think they may be more open new technologies,” von Hofe said.

Antigen Express uses a combination of three peptides, which are strands of linked amino acids, to develop its vaccines. Von Hofe said the company discovered that one of the peptides the company is using for its H5N1 vaccine, also in development, is from a part of the virus that is identical with H1N1. So now the company has to identify the other two peptides for the combination, get approval from U.S. and/or EU regulators to start trials and do the trials. This whole process should take more than a year, which means the company won’t be a player in this year’s fight against pandemic flu.

… Unless things go horribly, horribly wrong. Von Hofe said that if the swine flu mutates halfway through the season, and the vaccines being manufactured now are ineffective, the government could push up the time lines for other vaccines in development, including, perhaps, Antigen Express’ vaccine.

NewsFlash Roundup: Genzyme, NMT Medical, Ocean Spray

Monday, July 6th, 2009

In today’s NewsFlash Roundup, gadgets, biotech manufacturing and, as always, fruit juices.  

• Genzyme drug shortage aided by Israeli firm

The U.S. Food and Drug Administration has contacted Israel-based Protalix BioTherapeutics Inc. about the possibility of initiating a treatment protocol for use of its Phase 3 drug target for Gaucher’s disease. The drug has not yet been approved for use in the U.S. but would be used to blunt the effect that the Cerezyme shortage is having on patients, who have no other approved treatment options.

NMT Medical eyes conservative plans amid slow sales

The Boston-based company (Nasdaq: NMTI) said revenue for the second quarter that ended June 30 will be around $3.2 million, down from the $3.8 million to $4.3 million predicted in May.

From the print edition: Ocean Spray, Welch’s pursuing scientific claims of fruits

Ocean Spray Cranberries Inc. has won a patent for a method of extracting oil from the tiny seeds of cranberries, which the patent claims can be used for “treating or reducing the occurrence of breast cancer,” among other diseases. It’s a bold claim, but when asked if he believes the yellowish oil that smells and tastes faintly of cranberries could really have that power, inventor Wassef Nawar says, “Absolutely.” (more…)

Palomar wins FDA approval for wrinkle laser

Friday, June 5th, 2009

The Globe reports that Burlington-based Palomar Medical Technologies has won FDA approval for its laser, designed for use in the home to treat wrinkles around the eyes. What could go wrong?

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