Townhall.com, Where Your Opinion Counts
Talk Radio:   Bill Bennett   Mike Gallagher   Dennis Prager   Michael Medved   Hugh Hewitt   
TOP NEWS   LeftArrow - Townhall.com   RightArrow - Townhall.com  
Columns, funnies & more in your inbox!
Thursday, July 17, 2008
Family sues co. for muscular dystrophy drug
By FREDERIC J. FROMMER
Vote on It:
Average Vote:
[+] Text [-]
 
Poll
Prediction: Who will John McCain pick as his VP?








A Minnesota family is trying to force a New Jersey drug company to give their son an experimental drug for a fatal form of muscular dystrophy, saying he'll die without it.

The boy's mother, Cheri Gunvalson, who helped persuade Congress to significantly boost spending to find a cure for the disease, filed a lawsuit along with her husband and son in federal court in New Jersey this week.

Jacob Gunvalson, 16, suffers from Duchenne muscular dystrophy, a genetic, degenerative disease that mostly affects young boys. Typically, those who suffer from it die in their 20s because of weakness in their heart and lung muscles. There is no known cure, but the Gunvalson family believes the experimental drug holds hope.

The family claims that PTC Therapeutics of South Plainfield, N.J., repeatedly promised them Jacob would have access to the drug, known as PTC124, but then broke its word. The company denied ever making that assurance.

Jacob, who lost his ability to walk about a year ago, said in an interview that he thought he was going to get the drug many times.

"To think you can get help, and then just in the last second it's pulled out _ that's like getting your whole future hopes and all that smashed," he said Thursday.

Jacob hopes to one day become a psychiatrist or psychologist to help people facing "tough times."

"But it takes a lot of schooling to get done with that," he said, "and I don't know how much longer I have."

Chip Baird, PTC Therapeutics' chief financial officer, said the company sympathizes with the Gunvalsons and other families suffering from the disease, but that PTC has always communicated with the Gunvalsons "in a clear and consistent manner."

In 2001, Cheri Gunvalson teamed with the late Sen. Paul Wellstone, D-Minn., for passage of the MD CARE Act, which increased federal funding to study the disease. The legislation established several "centers of excellence" _ since renamed "Wellstone Centers" _ for muscular dystrophy research.

The family claims the company discouraged the Gunvalsons from enrolling Jacob in a preliminary, 28-day trial in 2005, saying it wouldn't hurt his chances of getting into a later study. It then used his absence from that original trial as a reason to disqualify him from a current study. Continued...

1 2
| Full Article & Comments | Next >
Share:
Vote on It:
Average Vote:
 
Sign Up to Post Your CommentsSign Up to Post Your Comments
If you are already registered, click here to login. Otherwise, please take a few seconds to register with Townhall.com. Once you sign up, you’ll be able to post your comments immediately, use the action center, get podcasts, and more!
Note: Fields marked with a red asterisk (*) are required.
Salutation:
First Name:
*
Last Name:
*
Email:
*
Nickname:
*
Note: Nick name will be shown when you post comments.
Address 1:
*
Address 2:
City:
*
State:
*
Zip:
*
Phone:
      
Your daily dose of conservative columns, editorial cartoons, talk radio, news, and more!
(Bi-Weekly) We highlight the best opportunities from our partners for surveys, action items and more.