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Biotech / Medical : ARIAD Pharmaceuticals -- Ignore unavailable to you. Want to Upgrade?


To: Mike McFarland who wrote (395)1/1/1999 6:39:00 AM
From: Henry Niman  Respond to of 4474
 
Mike, I just skimmed the patent and didn't see Epogen mentioned, but the patent is fairly broad.



To: Mike McFarland who wrote (395)1/1/1999 7:25:00 AM
From: Henry Niman  Respond to of 4474
 
I think that I skimmed the patent too quickly. It is quite broad.



To: Mike McFarland who wrote (395)1/1/1999 7:50:00 AM
From: Henry Niman  Respond to of 4474
 
Mike, I started of Transcription Regulation table under New Therapeutics at biocognizance.com
So far it just has the Science abstract, Bloomberg comments, and Aria patent, but will have more soon.



To: Mike McFarland who wrote (395)1/1/1999 12:28:00 PM
From: scaram(o)uche  Read Replies (1) | Respond to of 4474
 
Mike:

Thanks very much for raising this question. It's going to be an important one to have asked.

Here's claim one......

We claim:
1. A composition, comprising:

(a) recombinant AAV virions which comprise an AAV vector containing a nucleic acid molecule
encoding erythropoietin operably linked to control elements that direct the transcription and
translation thereof; and
(b) a pharmaceutically acceptable excipient.


This language clearly covers the ARIA work. I was surprised to see that the priority date was '96, sort of a fresh one.

OTOH, here's the abstract.....

The use of recombinant adeno-associated virus (AAV) virions for
delivery of DNA molecules to muscle cells and tissue in the treatment
of anemia is disclosed. The invention allows for the direct, in vivo
injection of recombinant AAV virions into muscle tissue, e.g., by
intramuscular injection, as well as for the in vitro transduction of
muscle cells which can subsequently be introduced into a subject for
treatment. The invention provides for sustained, high-level expression
of a delivered nucleotide sequence encoding erythropoietin, and for in
vivo secretion thereof from transduced muscle cells such that
systemic delivery is achieved.


Clearly, "sustained, high-level expression
of a delivered nucleotide sequence" is not in the spirit of the ARIA work. It'll be interesting!

Rick