CHOP Cancer Trials Support Unit Phase II Supplemental Payments

The Institution shall carry out the clinical trial research studies set forth in the above research protocol. The Study shall be conducted at the institution under the directionof PI named on Page 4 herein. The PI will oversee the regulatory aspects of the study at the institution by submitting protocols, amendments and safety reports to the IRB in a timely nammer, and ensure that all regulatory requirements are met. All regulatory documentation must be completed prior to enrollment of research subjects.