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To: Jibacoa who wrote (617)1/25/2007 1:09:58 PM
From: zeta1961Respond to of 802
 
You were reading my mind..I was wondering what would it take for INGN to commence combo Avastin trials..I also imagined the negotiations with Nance and DNA execs-g-

Thanks..very much looking forward to it..Looking forward to sharing un cafe with these folk-g-

cyclingnews.com

Elisabeth



To: Jibacoa who wrote (617)1/26/2007 2:29:08 PM
From: zeta1961Read Replies (1) | Respond to of 802
 
Bernard, I found the actual paper for the Mda7-Avastin mice studies..I'm more impressed than yesterday..caveat, I rarely get to read full length preclinicals so I don't have much to compare..Avastin was given by intraperitoneal route..

nature.com

In fact, the tumors in all of the Ad-mda7 plus bevacizumabtreated
mice completely regressed within the first 4 weeks (28
days) of initiation of treatment, and all of the mice remained
tumor free for an additional 48 days, at which time the
experiment was terminated. The tumor regression was consistent
in all animals treated with the combination, whereas no
complete regressions were observed in any other treatment
group. Moreover, adverse effects such as body weight loss,
morbidity, or death were evaluated for each agent and
combination. No decrease in body weight or morbidity was
observed, indicating that all treatments were tolerated. An
alternate method for evaluating effects of anticancer agents is to
analyze tumor growth delay (TGD), i.e., compare the time
required for tumors to achieve 200mm3.20 Both PBS and Ad-luc
controls gave a TGD of 8 days, whereas Ad-mda7 or
bevacizumab monotherapy produced a TGD of 12 days. The
combination of Ad-luc plus bevacizumab also demonstrated a
TGD of 12 days whereas Ad-mda7 plus bevacizumab treatment
produced a TGD of greater than 76 days. From our previous
experience with this model, if animals are tumor free for more
than 40 days, they do not regrow tumors and are cured.
These
results showed that treatment of lung tumors with Ad-mda7 plus
bevacizumab produces synergistic antitumor activity in vivo,
resulting in complete and prolonged tumor regression.