Phase 1 Dose Escalation Study of Autologous T-cells Genetically Modified at the CCR5 Gene by Zinc Finger Nucleases in HIV-Infected Patients

Status:	Completed
Conditions:	HIV / AIDS
Therapuetic Areas:	Immunology / Infectious Diseases
Healthy:	No
Age Range:	18 - Any
Updated:	3/1/2014
Start Date:	December 2009
End Date:	May 2014
Contact:	Ya-Li Lee
Email:	ylee@sangamo.com

A Phase 1 Dose Escalation, Single Dose Study of Autologous T-Cells Genetically Modified at the CCR5 Gene by Zinc Finger Nucleases SB-278 in HIV-Infected Patients Who Have Exhibited Suboptimal CD4+ T-Cell Gains During Long-Term Antiretroviral Therapy

This research study is being carried out to study a new way to possibly treat HIV. This
agent is called a "Zinc Finger Nuclease" or ZFN for short. ZFNs are proteins that can
delete another protein named CCR5. This CCR5 protein is required for certain types of HIV
(CCR5 tropic) to enter into and infect your T-cells. T cells are one of the white blood
cells used by the body to fight HIV. The most important of these are called "CD4 T-cells."

Some People are born without CCR5 on their T-cells. These people remain healthy and are
resistant to infection with HIV. Other people have a low number of CCR5 on their T-cells,
and their HIV disease is less severe and is slower to cause disease (AIDS).

Even with no detectable levels of HIV in the blood, HIV remains in some tissues in the body,
primarily the gut tissue. HIV infects the CD4+ T-cells including in the blood and gut. The
new treatment to be studied will involve removing white blood cell from the blood that
contains CD4+ T-cells. The extracted CD4+ T-cells are then genetically modified by the ZFNs
to be resistant to infection by HIV by removing the CCR5 gene from the surface of the CD4+ T
cell where HIV enters the cell. Additional genetically modified cells are manufactured and
then re-infused back into you. Researchers hope that these genetically modified cells will
be resistant to infection by HIV and will be able to reproduce additional resistant CD4+
T-cells in your body.

Laboratory studies have shown that when CD4+ T-cells are modified with ZFNs, HIV is
prevented from killing the CD4+ T-cells. On the basis of these laboratory results, thre is
the potential that ZFNs may work in humans infected with HIV and improve their immune system
by allowing their CD4+ T-cells to survive longer.

The purpose of this research study is to find out whether "zinc finger" modified CD4+
T-cells are safe to give to humans and find how "zinc finger" modified T-cell affects HIV.

Inclusion Criteria:

- Documented HIV infection prior to study entry

- Must be willing to comply with study-mandated evaluations; including not changing
their antiretroviral regimen (unless medically indicated) during the study period.

Cohort 1, 2 and 3 (Enrollment Completed)

Cohort 5:

- Must have received HAART therapy, and had undetectable viral loads for at least 1
year.

- HIV-1 RNA < 50 copies/mL obtained within 60 days prior to study entry performed with
an ultrasensitive HIV-1 PCR assay.

- CD4+ T cell count >350 cells/mm3

- Heterozygous for the CCR5 delta-32 mutation

- On stable antiretroviral medication (no changes to treatment within 4 weeks of
screening and willing to discontinue current antiretroviral therapy during the
structured therapy interruption

Cohort 4

- On stable antiretroviral medication (no changes to treatment within 4 weeks of
screening and willing to continue on current antiretroviral therapy through week 8
after infusion

- CD4+ T cell count >350 cells/mm3.

- HIV-1 >1,000 copies/mL at screen and not responding to current antiviral therapy
(i.e. HIV-RNA plasma levels > 1000 copies/ml after at least 12 weeks of stable,
unchanged ARV therapy).

Exclusion Criteria:

- Acute or chronic hepatitis B or hepatitis C infection

- Active or recent (in prior 6 months) AIDS defining complication.

- Any cancer or malignancy within the past 5 years, with the exception of successfully
treated basal cell or squamous cell carcinoma of the skin or low grade (0 or 1) anal
or cervical dysplasia.

- Current diagnosis of NYHA grade 3 or 4 CHF, uncontrolled angina or uncontrolled
arrhythmias.

- History or any features on physical examination indicative of a bleeding diathesis.

- Previous treatment with any HIV experimental vaccine within 6 months prior to
screening, or any previous gene therapy using an integrating vector.

- Use of chronic corticosteroids, hydroxyurea, or immunomodulating agents (e.g.,
interleukin-2, interferon-alpha or gamma, granulocyte colony stimulating factors,
etc.) within 30 days prior to enrollment

- Breast-feeding, pregnant or unwilling to use acceptable methods of birth control for
6 months following the last infusion of SB-728-T cells.

- warfarin or any other medication that is likely to affect platelet function or other
aspects of blood coagulation during the 2 week period prior to leukapheresis.

- Active drug or alcohol use or dependence

- Serious illness requiring systemic treatment and/or hospitalization within 30 days
prior to study entry.

- Recent vaccination or intercurrent illness (within 5 weeks prior to infusion)

- Have an allergy or hypersensitivity to study product excipients (human serum albumin,
DMSO and Dextran 40).

- Subjects who are currently taking maraviroc or have received maraviroc within 6
months prior to screening.

Cohort 4 only:

- HIV-1 RNA >1,000 copies/mL at screen and not responding to current antiviral therapy

- CD4+ T cell count >350 cells/mm3

We found this trial at

sites

Central West Clinical Research, Inc.

St Louis, Missouri 63108

from

St Louis, MO