percent; no patient achieved an objective
response. The median PFS was 2.3 months. Three patients had a >6 month PFS.
The disease control and median PFS are similar to results achieved in this
patient population for approved agents (panitumumab or cetuximab
monotherapy).
Safety data were qualitatively similar to that of irinotecan and a
fluoropyrimidine with neutropenia, diarrhea, nausea, vomiting and fluid
loss events (dehydration and hypokalemia) being the most common. The 210
unit/m2 dose produced more toxicities than seen in the CPX-1 Phase 1
clinical trial, resulting in only 40 percent of patients receiving >80
percent of the planned dose intensity. Treatment will be initiated at a
lower dose in future studies.
"The efficacy results in this study are very encouraging, particularly
compared to historical data," said Arthur Louie, M.D., chief medical
officer of Celator. "These data support that drug ratios may play an
important role when combining drugs to treat patients. This study shows
that well established drugs with proven activity may offer greater clinical
benefit when a synergistic ratio is identified and the individual drugs are
locked into a drug delivery vehicle able to deliver and maintain the
desired ratio in patients. Our goal is to substantially improve clinical
outcomes by using our proprietary CombiPlex(TM) technology."
About Celator
Celator Pharmaceuticals, Inc., is a privately held pharmaceutical
company working to develop new and more effective therapies to treat
cancer. CombiPlex(TM), the company's drug ratio technology platform,
represents a revolutionary new approach that identifies a ratio of drugs
that will deliver a synergistic benefit, locks the desired ratio in a drug
delivery vehicle and maintains the ratio in patients with the goal of
improving clinical outcomes. The company pipeline includes: CPX-1 (a
liposomal formulation of irinotecan:floxuridine), currently in a Phase 2
trial in patients with colorect
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SOURCE Celator Pharmaceuticals Copyright©2008 PR Newswire. All rights reserved | |
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