Once an IND is filed, FDA has 30 days to comment before the Company can begin Phase I trials The FDA has regularly been very helpful. It is important for Advaxis to comprehend the regulatory perspective, and the assistance we have received provides improved our advancement program in many ways, commented Advaxis Executive Vice President John Rothman. Because each brand-new construct is based on live attenuated Listeria monocytogenes, every successful interaction with the FDA strengthens the regulatory framework because of this entire new class of immunotherapies. .. Advaxis completes ADXS-PSA prostate cancer construct pre-IND ending up in the FDA Advaxis, Inc., , a head in developing the next generation of immunotherapies for malignancy and infectious illnesses, has completed a pre-IND meeting with the FDA on August 10 to go over the development arrange for ADXS-PSA, a construct for the treating prostate tumor.‘It really is apparent that accelerated partnerships are critical to making sure elimination goals, because of Dr. Roly Gosling and the Global Health Group at UCSF because of this timely insight,’ Chesire concludes . This content was reprinted from kaiserhealthnews.org with permission from the Henry J. Kaiser Family members Foundation. Kaiser Health News, an editorially independent information service, is an application of the Kaiser Family members Foundation, a nonpartisan health care policy research organization unaffiliated with Kaiser Permanente.