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September 04, 2010, 08:34:52 PM
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Three products now FDA-approved!
- Cinryze, approved to prevent HAE attacks.
- Berinert, approved for treating acute facial and abdominal HAE attacks
- Kalbitor, approved for treating acute attacks in patients 16 yrs and older. The product is delivered through subcutaneous injections

Please contact the HAEA's Patient Services group for more information

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| | |-+  DX-88 (ecallantide)
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Author Topic: DX-88 (ecallantide)  (Read 360 times)
lmgardner
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Posts: 2

« on: November 01, 2009, 08:30:37 AM »

I have been involved in the clinical trials with DX-88 for years and have been anxiously awaiting its FDA approval.  Now my study coordinator has informed me that it will not be approved for home administration.  I am so disappointed and discouraged.  When I have an abdominal attack the last thing that I want to do is leave the comforts of home and head to my MD office or ER. 

I sent two letters to Paul Fletcher of Dyax but have not received a response.  I was not able to attend the conference in Orlando.  Was there any new information released regarding DX-88?  Is my information accurate?  Is there anything that I can do to challenge this decision?
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