SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Biotech / Medical : T/FIF Portfolio -- Ignore unavailable to you. Want to Upgrade?


To: Henry Niman who wrote (530)2/8/1999 6:29:00 PM
From: scaram(o)uche  Read Replies (1) | Respond to of 1073
 
I just posted the header and time stamp, Henry.

Thursday December 31, 1:38 PM (EST)

Gene therapy with molecular switch opens new possibilities

WASHINGTON, Dec 31 (AFP) - Using a unique combination of cutting-edge
technologies, scientists
have introduced a new gene therapy that will make a number of new
treatments possible, a report
in Science magazine said Thursday.

The novel therapy introduces therapeutic genes into the body and then
controls them with a drug
given as a simple pill.

What the research shows is an entirely new form of drug delivery through
a harmless virus
acting as a carrier of a molecular switch that can control the gene.

Reeseachers at the University of Pennsylvania Medical Center and ARIAD
Pharmaceuticals in
Cambridge, Massachusetts, developed the technique which has been
successfully tested on monkeys
and mice.

"It's a very precise gene switch, a kind of molecular rheostat," Dr
James Wilson of
Pennsylvania Medical Center explained. A common rheostat is the dimmer
switch used in household
lights.

"We're excited about these results, because they create new
opportunities for experimental and
then clinical applications of gene threapy that we couldn't consider
before," said Wilson,
director of the Institute for Human Gene Therapy at Penn, and senior
author of the Science
report.

The system couples advances at Penn allowing long-term introduction of
genes into the body with
ARIAD's patented technology to regulate gene activity.

"The ability to achieve dosage control of a drug in the context of gene
therapy is going to be
critical to making a number of new treatments possible," Michael Gilman,
chief scientific
officer at ARIAD said.

The new method has distinct advantages over current drug delivery
systems, Gilman said.

With oral or injectable drugs, the patient has peaks and valleys in the
amount of drug in the
blood.

"One of the real advantages of using gene therapy to deliver drugs is
that you can deliver them
in a steady trickle that can be adjusted through administration of a
pill," Gillman added.

The next step, researchers say, will be clinical trials.

pa/smb/ld



To: Henry Niman who wrote (530)2/8/1999 6:34:00 PM
From: scaram(o)uche  Respond to of 1073
 
>> I based the conclusion of the facts that I was given <<

No, Henry, you made a conclusion based on an incorrect assumption and on incomplete data. You not only made a conclusion, you also made an accusation. You owe me an apology rather than more rationale.