Advaxis doses first patient in FDA-approved stage II CIN trial Advaxis.

Advaxis doses first patient in FDA-approved stage II CIN trial Advaxis, Inc., , the live, attenuated Listeria monocytogenes biotechnology company, has dosed the first patient in its US Food and Medication Administration -approved, phase II scientific trial in cervical intraepithelial neoplasia , known as cervical dysplasia commonly. The dosing was administered at the website of Dr . Keith Aqua, M.D. Of the Institute for Women’s Wellness & Body. Dosing the 1st patient is a significant milestone for our firm, commented Advaxis Chairman/CEO Thomas A. Moore. It really is a highly awaited development amongst all Advaxis and immunotherapy fans, at large; following a recent Dendreon Company FDA approval.

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