Gene Therapy for Painful Diabetic Neuropathy

• ClinicalTrials.gov Identifier: NCT01002235
• Recruitment Status: Completed
• First Posted: October 27, 2009
• Last Update Posted: October 24, 2019
• Sponsor: Helixmith Co., Ltd.
• Information provided by (Responsible Party): Helixmith Co., Ltd.

Study Description

Brief Summary:

The purpose of this study is to assess the safety and tolerability of injecting VM202 in the leg muscle in patients with painful diabetic neuropathy (DPN). The study will also assess the potential of VM202 to reduce the pain associated with DPN.

Condition or disease	Intervention/treatment	Phase
Painful Diabetic Neuropathy	Biological: VM202	Phase 1; Phase 2

Detailed Description:

Peripheral neuropathy is a serious complication of diabetes. This form of neuropathy carries a high risk of pain, trophic changes and autonomic dysfunction.

Currently, there are no approved drugs or interventional strategies known to halt or reverse the progression of DPN. Treatments target pain reduction, physical function improvement, reduction of psychological distress, and quality of life improvements.

There is currently no effective treatment for diabetic neuropathy, and good glycemic control is the only way to minimize the risk of occurrence. Clearly, it would be desirable to prevent, impede, or reverse the disrupting and often life-threatening manifestations of peripheral neuropathy by stimulating growth or regeneration of peripheral nerve axons.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 12 participants
• Allocation: Non-Randomized
• Intervention Model: Sequential Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Phase I/II, Open Label, Dose-Escalation Study to Assess the Safety and Tolerability of VM202 in Patients With Painful Diabetic Peripheral Neuropathy
• Study Start Date: February 2010
• Actual Primary Completion Date: April 2011
• Actual Study Completion Date: April 2012

Arms and Interventions

Arm	Intervention/treatment
Experimental: Cohort 1; Two divided doses of VM202 injected into the calf muscle on Day 0 and Day 14 for a total dose of 4 mg.	Biological: VM202; Intramuscular injections in the calf on Day 0 and Day 14.
Experimental: Cohort 2; Two divided doses of VM202 injected into the calf muscle on Day 0 and Day 14 for a total dose of 8mg.	Biological: VM202; Intramuscular injections in the calf on Day 0 and Day 14.
Experimental: Cohort 3; Two divided doses of VM202 injected into the calf muscle on Day 0 and Day 14 for a total dose of 16mg.	Biological: VM202; Intramuscular injections in the calf on Day 0 and Day 14.

Outcome Measures

Primary Outcome Measures :

1. Dose limiting toxicity [ Time Frame: Day 0 post-dose, Days 14, 21, 30, 60, 90, Month 6 and 12 ]
   Measurement of Adverse events and serum levels of HGF.

Secondary Outcome Measures :

1. Pain Levels [ Time Frame: Days 0, 14, 30, 60, 90, 180, 365 ]
   Change in pain level as measured by the VAS, SF-MPQ and BPI-DPN and the status of preexisting ulcers will also be reported.

Eligibility Criteria

• Ages Eligible for Study: 18 Years to 75 Years (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Criteria

Inclusion Criteria:

• Age ≥ 18 years to 75 years
• Documented history of Type I or II diabetes with current treatment control (glycosylated hemoglobin A1c of ≤ 10.0%)
• Diagnosis of painful diabetic peripheral neuropathy in both lower extremities
• The physical examination component of the Michigan Neuropathy Screening Instrument Score (MNSI) is ≥ 3 at Screening
• Visual analog scale (VAS) score of ≥ 4 cm at Screening (0 cm = no pain - 10 cm worst imaginable pain)
• Stable treatment of diabetes for at least 3 months with no anticipated changes in medication regimen, and no new symptoms associated with diabetes
• Lower extremity pain for at least 6 months
• If female of childbearing potential, negative pregnancy test at screening and using acceptable method of birth control during the study.

Exclusion Criteria:

• Peripheral neuropathy caused by condition other than diabetes;
• Other pain more severe than neuropathic pain;
• Progressive or degenerative neurological disorder;
• Myopathy;
• Inflammatory disorder of the blood vessels (inflammatory angiopathy, such as Buerger's disease);
• Active infection;
• Chronic inflammatory disease (e.g. Crohn's, Rheumatoid Arthritis)
• Positive HIV or HTLV at Screening
• Positive Hepatitis B or C as determined by Hepatitis B core antibody (HBcAB), antibody to Hepatitis B antigen (IgG and IgM; HbsAB), Hepatitis B surface antigen (HBsAg) and Hepatitis C antibodies (Anti-HCV), at Screening or known immunosuppression or on chronic treatment with immunosuppressive drugs, chemotherapy or radiation therapy
• Stroke or myocardial infarction within last 6 months;

• Ophthalmologic conditions pertinent to proliferative retinopathy or conditions that preclude standard ophthalmologic examination:

  • Cataract surgery within 6 months of trial;
  • Vascular lesions of the anterior segment of the eye (infection or ulceration of the cornea, rubeotic glaucoma, etc);
  • Vascular lesions of the posterior segment of the eye or proliferative retinopathy, macular edema, s/p photocoagulation for macular edema or proliferative retinopathy; sickle cell retinopathy, ischemic retinopathy due to retinal venous stasis or carotid artery disease;
  • Choroidal angiogenesis; and
  • Large elevated choroidal nevi, choroidal vascular tumors (choroidal hemangioma), or melanomas.
• Specific laboratory values at Screening including: Hemoglobin < 9.0 g/dL, WBC < 3,000 cells per microliter, platelet count <75,000/mm3, Creatinine > 2.0 mg/dL; GFR < 50, AST and/or ALT > 2 times the upper limit of normal or any other clinically significant lab abnormality which in the opinion of the investigator should be exclusionary;
• Use of gamma-linolenic acid (GLA), alpha lipoic acid or any other high dose dietary antioxidant supplement for symptomatic relief of DPN;
• Uncontrolled hypertension as defined as sustained systolic blood pressure (SBP) > 200 mmHg or diastolic BP (DBP) > 110 mmHg at baseline/screening evaluation;
• Patients with history of or new screening finding of malignant neoplasm except basal cell carcinoma or squamous cell carcinoma of the skin (if excised and no evidence of recurrence);
• Malignant tumors or abnormal screening test suspicious for cancer, or patients in whom screening exams indicate possible occult malignancy unless malignancy has been ruled out. Patients with family history of colon cancer in any first degree relative unless they have undergone a colonoscopy in the last 12 months with negative findings;
• Elevated PSA unless prostate cancer has been excluded;
• Subjects requiring > 81 mg daily of acetylsalicylic acid; If > 81 mg are taken at screening, subjects may be enrolled if willing/able to switch to another medication;
• Major psychiatric disorder in past 6 months;
• History of drug or alcohol abuse / dependence in the past 2 years;
• History of recent tobacco abuse (within past 5 years);
• BMI > 38 kg/m2;
• Use of an investigational drug or treatment in past 12 months; and
• Unable or unwilling to give informed consent.

Contacts and Locations

Locations

United States, California

Diablo Clinical Research Hospital

Walnut Creek, California, United States, 94598

United States, Illinois

Northwestern Memorial Hospital

Chicago, Illinois, United States

Sponsors and Collaborators

Helixmith Co., Ltd.

Investigators

• Principal Investigator: John Kessler, M.D.; Northwestern Memorial Hospital

More Information

• Responsible Party: Helixmith Co., Ltd.
• ClinicalTrials.gov Identifier: NCT01002235 History of Changes
• Other Study ID Numbers: VMDN-001/D
• First Posted: October 27, 2009
• Last Update Posted: October 24, 2019
• Last Verified: October 2019

Keywords provided by Helixmith Co., Ltd.:

Diabetic; Neuropathy; peripheral; diabetes

Additional relevant MeSH terms:

Peripheral Nervous System Diseases; Diabetic Neuropathies; Pain; Neuromuscular Diseases; Nervous System Diseases; Neurologic Manifestations; Signs and Symptoms; Diabetes Complications; Diabetes Mellitus; Endocrine System Diseases