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Aeterna Zentaris
AEZS today presented encouraging
preclinical results for disorazol Z cytotoxic conjugates, such as
AEZS-125, in ovarian cancer. Results showed the compound's high
potential for the treatment of luteinizing hormone-releasing hormone
(LHRH) receptor positive tumors. Data were presented by the Company's
Director of Preclinical Development, Babette Aicher, PhD, during a
poster presentation at the 24th EORTC-NCI-AACR (ENA) Symposium on "Molecular Targets and Cancer
Therapeutics", currently held in Dublin, Ireland. The study is funded
through a grant from the German Ministry of Education and Research.
Juergen Engel, PhD, Aeterna Zentaris President and CEO stated,
"Disorazol Z cytotoxic conjugates such as AEZS-125, are an extension of
our AEZS-108 innovative LHRH receptor targeted platform in oncology.
These encouraging results presented at the ENA Symposium will enable us
to select a specific drug candidate for further preclinical development
expected to start in the first quarter of 2013."
Conclusions
All conjugates of D-Lys6 -LHRH and disorazol Z analyzed, demonstrated high potential
regarding the treatment of LHRH-receptor positive tumors;
For all conjugates, including AEZS-125, proof-of-concept could be
demonstrated in an
LHRH-receptor positive A2780 ovarian cancer xenograft model;
Experiments are currently under way addressing:
Correlation of tumor LHRH-receptor expression and treatment efficacy;
Evaluation
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