Advertisement EntreMed gets FDA's nod for clinical trials of antitumor drug - Pharmaceutical Business review
Pharmaceutical Business review is using cookies

ContinueLearn More
Close

EntreMed gets FDA’s nod for clinical trials of antitumor drug

EntreMed has received FDA's approval of investigational new drug application for its aurora kinase or angiogenesis inhibitor, ENMD-2076.

ENMD-2076 is a novel, dual-acting, kinase inhibitor with potent activity against Aurora A and tyrosine kinases linked to promoting cancer and inflammatory diseases. The company claims that ENMD-2076 has demonstrated substantial, dose-dependent efficacy as a single agent in multiple xenograft models, including tumor regression in breast, colon, and leukemia models. Importantly, ENMD-2076 is an oral agent that has shown an acceptable toxicity profile in preclinical studies without cardiovascular effects.

Carolyn Sidor, vice president and chief medical officer of EntreMed, said: “Acceptance of the IND application for ENMD-2076 initiates the clinical program for our first compound that targets kinases. We plan to initiate several clinical studies with ENMD-2076 that include Phase I trials in both solid and hematological cancers in 2008.”