Food and Drug Administration

BIOLOGICAL RESPONSE MODIFIERS ADVISORY COMMITTEE

October 26, 2001

Briefing Information

Food and Drug Administration

A Phase 1 Open-Label Clinical Trial of the Safety and Tolerability of Single Escalating Doses of Autologous T Cells Transduced with VRX496 in HIV Positive patient-Subjects: Cover Sheet, Contents  pdf

RAC Review of Protocol #0107-488, Nancy M. P, King, JD   pdf   htm

Protocol 0107-488, A Phase 1a, randomized study of escalating single doses of VRX496 in subjects with AIDS, R. R. MacGregor   pdf   htm

Review of 0107-488, PI: Rob Roy MacGregor MD, Sponsor: VIRxSYS Corp "A phase I open-label clinical trial of the safety and tolerability of single escalating doses of autologous CD4 T cells transduced with VRX496 in Hiv positive subjects,"  M. Louise Markert, MD, PhD.   pdf   htm

Protocol 0107-488, A Phase 1a, randomized study of escalating single doses of VRX496 in subjects with AIDS, R R MacGregor   pdf   htm

Reply to Dr. King's comments our Protocol #01-07-488. "A phase 1 open label clinical trial of the safety and tolerability of single escalating doses of autologous T cells transduced with VRX496 in HIV positive patients." Rob Roy MacGregor, MD, Carl H June, MD, Boro Dropulic PhD   pdf   htm

Proposed protocol: Ex-vivo gene transfer of VRX496 into HIV-infected patient-subjects   pdf

A Phase 1 Open Label Clinical Trial of the Safety and Tolerability of Single Escalating Doses of Autologous T Cells Transduced with VRX496 in HIV Positive Patients, Patient Consent Form   pdf

September 25, 2001 letter to Boro Dropulic, PhD, VIRxSYS Corporation from  Amy P. Patterson, MD, Director, Office of Biotechnology, NIH re: Public RAC Discussion of Protocol #0107-488   pdf   doc

VIRxSYS Corporation Investigational New Drug Protocol, VRX496-01-01, Final, Date Prepared:  September 5, 2001   pdf

Transcript of September 6, 2001, Afternoon Session, pages 201-325, "Discussion of Human Gene Transfer Protocol #01007-488 Entitled: A Phase I, Open-Label Clinical Trail of the Safety and Tolerability of Single Escalating Doses of Autologous CD4 T Cells Transduced with VRX496 in HIV-Positive Subjects"   pdf   htm

VIRxSYS Corporation

Disclaimer

The statements contained in this document(s) are those of the product's sponsor, not FDA, and FDA does not necessarily agree with the sponsor's statements. FDA has not made a final determination about the safety or effectiveness of the product described in this document.

Briefing Document   pdf

October 26, 2001 Letter to The Editor, Molecular Therapy from Boro Dropulic, VIRxSYS Corporation   pdf