Stem Cell Mobilization in Diabetic Neuropathy Subjects Receiving SB-509

A Phase 2 Study of Stem-Cell-Mobilization in Subjects With Diabetic Neuropathy Receiving SB-509

Sponsors

Lead Sponsor: Sangamo Therapeutics

Source Sangamo Therapeutics
Brief Summary

The primary and secondary objectives of this study are:

Primary: To evaluate stem-cell-mobilization in subjects with diabetic neuropathy receiving SB-509. Stem cell mobilization will be assessed by evaluating the presence of stem cells circulating in peripheral blood.

Secondary: To evaluate the safety of SB-509 in subjects treated with SB-509 with diabetic neuropathy; and to compare the effect of SB-509 versus placebo on a pre-defined multi-endpoint analysis that includes visual analog scale for pain intensity (VASPI), total neuropathy score (TNS), evoked nerve conduction velocity (NCV) and quantitative sensory testing (QST)

Detailed Description

SB-509 contains the gene (DNA-a kind of biological "blueprint") for a protein. When a researcher injects SB-509 into your legs, the drug enters the muscle and nerve cells around the injection site and causes these cells to make a protein. This protein causes your cells to increase production of another protein called vascular endothelial growth factor (VEGF), which may improve the structure and function of nerves. In addition, there are changes in the levels of 28 additional proteins in your cells. These proteins function to promote the growth of cells, are structures in cells, help synthesize products, and affect immune cells, and some have unknown functions. This increase in your own VEGF proteins may protect and repair the damaged nerves caused by diabetic neuropathy.

This study is intended to further evaluate the mechanism of SB-509 action.

Overall Status Completed
Start Date January 2008
Completion Date October 2009
Primary Completion Date October 2009
Phase Phase 2
Study Type Interventional
Primary Outcome
Measure Time Frame
Stem cells circulating in peripheral blood One year
Secondary Outcome
Measure Time Frame
Safety and Efficacy of SB-509 One year
Enrollment 23
Condition
Intervention

Intervention Type: Drug

Intervention Name: SB-509

Description: Active drug

Arm Group Label: 1

Intervention Type: Drug

Intervention Name: SB-509

Description: Active drug

Arm Group Label: 2

Intervention Type: Drug

Intervention Name: Placebo

Description: Placebo

Arm Group Label: 3

Intervention Type: Drug

Intervention Name: SB-509

Description: Active drug

Arm Group Label: 4

Eligibility

Criteria:

Inclusion Criteria:

Key Inclusion Criteria:

- Have a clinical diagnosis of diabetes mellitus type I or II for at least 12 months prior to the study.

- Have received a diagnosis of sensorimotor diabetic neuropathy from a neurologist (a doctor who specializes in disorders of the nervous system) or endocrinologist (a doctor who specializes in diabetes).

- Have reduced nerve conduction velocity in any lower extremity nerve: peroneal, tibial or sural due to diabetic polyneuropathy

- If female and of childbearing potential, agree to use a medically acceptable physical barrier method during the study.

- Have blood pressure < 140/90 mm Hg

- Body mass index (BMI) < 38 kg/m2

Key Exclusion Criteria:

Subjects with the following are NOT eligible to participate in this study:

- Have moderate to severe ischemic heart disease, any history of congestive heart failure, or have had a myocardial infarction (heart attack) within the previous 6 months.

- Have chronic foot or leg ulcers for >1 month, gangrene in the legs, or any previous amputation of the lower extremity.

- Have a history of cancer within the past 5 years (except for curable non-melanoma cancer of the skin, superficial bladder cancer in complete remission, or any other cancer that has been in complete remission for at least 5 years).

- Have colon polyps. If patients have a history of benign colonic polyps that have been removed, they must have evidence of a normal colonoscopy within the last 12 months.

- Require any drug that depresses patients' immune systems (such as methotrexate, cyclophosphamide, or cyclosporine) when they receive the study drug and for 30 days afterwards.

- Have a known disorder that affects patients' immune systems (such as HIV/AIDS, hepatitis B virus [HBV], hepatitis C virus [HCV], sarcoidosis, tuberculosis, rheumatoid arthritis, or autoimmune disorders).

Gender: All

Minimum Age: 18 Years

Maximum Age: 70 Years

Healthy Volunteers: No

Location
Facility:
| La Jolla,, California, 92037, United States
| Walnut Creek, California, 94598, United States
| Houston, Texas, 77030, United States
| San Antonio, Texas, 78229, United States
Location Countries

United States

Verification Date

October 2012

Responsible Party

Name Title: Ely Benaim, M.D., Vice President, Clinical Affairs

Organization: Sangamo BioSciences, Inc.

Keywords
Has Expanded Access No
Condition Browse
Number Of Arms 4
Arm Group

Label: 1

Type: Experimental

Description: Cohort 1

Label: 2

Type: Experimental

Description: Cohort 2

Label: 3

Type: Placebo Comparator

Description: Cohort 3

Label: 4

Type: Experimental

Description: Cohort 4

Study Design Info

Allocation: Randomized

Intervention Model: Parallel Assignment

Primary Purpose: Treatment

Masking: Single (Participant)

Source: ClinicalTrials.gov