Advance AP24534 and Innovative Oncology Pipeline 
ARIAD expects to report clinical proof-of-concept data in 2009 for its second 
oncology product candidate, AP24534, currently being evaluated in a 
multi-center Phase 1 trial of patients with drug-resistant and refractory 
hematological malignancies, including chronic myeloid leukemia (CML) and acute 
myeloid leukemia (AML). AP24534 is an oral, multi-targeted kinase inhibitor 
that is designed for use in a variety of cancer types. Preclinical data of 
AP24534 reported last year show that this product candidate potently inhibits 
the kinase targets associated with drug-resistant CML, including all known 
mutant variants of the target protein, Bcr-Abl, as well as targets associated 
with AML. The potential of AP24534 in specific solid tumors will also be 
explored through additional clinical studies.

--- On Mon, 12/15/08, educatorsusan <[email protected]> wrote:


From: educatorsusan <[email protected]>
Subject: [CMLHope] trials and drugs
To: "CMLHope" <[email protected]>
Date: Monday, December 15, 2008, 9:39 PM



Okay, I have lurked long enough.  I want to respond to everyone and
just kept quiet.  My husband and I ventured out for my bi-annual sixth
month check up from Miami, Florida to Portland, Oregon to see Dr.
Druker.  Of course, my status remains super.  I listen to your stories
of woe and wonder what I would do if I was in your shoes.

Jeff, in regards to this trial...I would ask or go see Dr. Druker if
you have the 1315 mutation.  While we were out there, Dr. Druker was
estatic!  Since last Spring, he was working on a drug that was thought
to only work in combination with another drug, whether it was gleevec
or dastinab or nilotinab, etc.  However, his drug is working on
mutations by itself!!!  This is wonderful news he says to those who
have mutations.

I am happy that I am doing so well.  I was also told I would never
need another BMB/BMA as long as my numbers stay the same!

I still get eyebleeds, and a little swelling.  I have had all the side
effects from Gleevec.  So if you ever need to write me for the answers
that Dr. Druker and Carolyn (Dr. Druker's assisant/nurse) gave to me
please email me at [email protected].  I would be please to help
you out.  I had everything BUT the rash!!!  When I say everything, I
mean everything.  Dr. Druker says that I was his top 10% for all
patients to have so many reactions.

Now, I am really fairing pretty nicely!

Hugs,
Susan Rosenthal Miami, Florida
dx. January 8th, 2003
Began Gleevec: 4/10/2003
Ceased Gleevec: 4/21/2003
"Rebegan" Gleevec: 4/25/2003
Tranfusion dependent: May 2004-November 2005
Gleevec reduced to 400mg: 8/2004
Gleevec reduced to 300mg: 8/2005
Gleevec reduced to 200/300 alternating days: November 7, 2006 to
present day except now I am taking 250 every day now...
Still undetectable 9/24/2008
March 27, 2008 BMB/BMA PCRU!!! FISH 0% YEAH!!!!!
Next appointment with Dr. Druker:  Thursday, October 23, 2008
Gleevec PK Level taken every 3 months monitored by Novartis and Dr.
Druker.
PCR-in June was a weak positive but Dr. Druker felt that it was the
same as undetectable...but will repeat PCR sooner in August 2008
I was told that I would not need another BMB as long as my numbers
stay where they are!!! YIPEEEE!




      
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