Ad5.hAC6 Gene Transfer for CHF
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Purpose
This research study is designed to determine: 1) whether gene transfer using an agent called Ad5.hAC6 (adenovirus-5 encoding human adenylyl cyclase type 6) can be given safely to patients with congestive heart failure (CHF) and 2) whether this agent may be of benefit in heart failure. Gene transfer is an idea in which genes are introduced into cells and the cells then produce the specific protein that the gene directs, in this case, a protein known as adenylyl cyclase type 6 (AC6). The gene is carried into the heart cells by a modified virus. The virus that is modified is an adenovirus (Ad5), a virus that sometimes causes a brief cold. In extensive animal experiments, it was found that increased amounts of AC6 protein in heart cells appeared to make the heart pump more vigorously.
| Condition | Intervention | Phase |
|---|---|---|
|
Congestive Heart Failure |
Drug: Ad5.hAC6 |
Phase 1 Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Phase I/II Study AC6 Gene Transfer for Congestive Heart Failure |
- Combined: a) Exercise treadmill time; b) LV function by echocardiography before and during dobutamine infusion; c) Rate of LV pressure development and decline (dP/dt and -dP/dt) before and during dobutamine infusion. [ Time Frame: Before, 4w, 12w ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 72 |
| Study Start Date: | July 2010 |
| Estimated Study Completion Date: | December 2014 |
| Estimated Primary Completion Date: | December 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Ad5.hAC6
Will receive intracoronary adenovirus encoding human adenylyl cyclase type 6
|
Drug: Ad5.hAC6
Intracoronary delivery of Ad5.hAC6 or sucrose solution (placebo) in 3:1 randomization (Ad5.hAC6 : placebo) with dose escalation, starting at 3.2 x 10^9 vp to 3.2 x 10^12 vp in 6 dose groups
|
|
Placebo Comparator: sucrose solution
Will receive intracoronary sucrose solution
|
Drug: Ad5.hAC6
Intracoronary delivery of Ad5.hAC6 or sucrose solution (placebo) in 3:1 randomization (Ad5.hAC6 : placebo) with dose escalation, starting at 3.2 x 10^9 vp to 3.2 x 10^12 vp in 6 dose groups
|
Detailed Description:
This research study is designed to determine: 1) whether gene transfer using an agent called Ad5.hAC6 (adenovirus-5 encoding human adenylyl cyclase type 6) can be given safely to patients with congestive heart failure (CHF) and 2) whether this agent may be of benefit in heart failure. Gene transfer is an idea in which genes are introduced into cells and the cells then produce the specific protein that the gene directs, in this case, a protein known as adenylyl cyclase type 6 (AC6). The gene is carried into the heart cells by a modified virus. The virus that is modified is an adenovirus (Ad5), a virus that sometimes causes a brief cold. In extensive animal experiments, it was found that increased amounts of AC6 protein in heart cells appear to make the heart pump more vigorously.
Eligibility| Ages Eligible for Study: | 18 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
- Male or non-pregnant female patients aged 18-80 years of age
- ≥3-month history of heart failure
- Compensated (stable) CHF not on intravenous inotropes, vasodilators or diuretics, on optimal medical and device therapy as defined by AHA/ACC Guidelines
- LV ejection fraction (on optimal therapy) no greater than 40%
- Implanted cardiac defibrillator
- At least one major coronary artery (or graft) with <50% proximal obstruction
- Maximal exercise (in estimated METs) on treadmill testing must not exceed 65% of age-predicted maximum [ Predicted METs = 15 - (Age/10) ]. Patients unable to walk (spinal injury, orthopedic problems) can be enrolled if all other criteria are met.
- Women of child-bearing capacity must have a negative pregnancy test within 2 days of test substance administration, and female and male patients must be willing to use birth control during sex for 12w after test substance administration if the female partner is of child-bearing capacity.
- Subjects willingly provide informed consent consistent with ICH-GCP guidelines
Exclusion Criteria
- Unstable or Class IV angina
- Coronary revascularization planned or predicted in next 6 months
- Ischemic myocardium in 3 or more regions of a single perfusion bed, as assessed by stress echocardiography or jeopardized viable myocardium >15% on perfusion imaging.
- ≥50% occlusion of an "unprotected" left main coronary artery. If arterial or venous conduits provide blood flow to the distal left coronary circulation (ie, patent bypass grafts) then left main disease is "protected" and such patients are not excluded. The cardiologist performing the cardiac catheterization will make these decisions.
- 2° AV Block (Mobitz 2) or 3° AV block unless pacemaker is present
- Hospitalization for CHF requiring intravenous inotropes or vasodilators in the past 4 weeks
- History of biopsy proven myocarditis
- Myocardial infarction in previous 6 months
- Restrictive, hypertrophic or infiltrative cardiomyopathy or chronic pericarditis
- Previous or planned organ transplant recipient or donor.
- Thrombocytopenia (<100,000 platelets/µl) or bleeding diathesis
- COPD requiring supplemental oxygen at home
- AST > 2 times upper limit of normal or chronic liver disease such as cirrhosis or Hepatitis C Virus (HCV). Patients with HCV are eligible only if both of two conditions are met: a) liver function tests are normal; AND b) liver biopsy is normal or shows only mild fibrosis.
- Current or predicted hemodialysis within 12 months or estimated glomerular filtration rate (EGFR) <30 ml/min. On online EGFR calculator that uses sex, age, body weight and serum creatinine is available at: www.kidney.org/professionals/kdoqi/gfr_calculator.cfm. Use the higher of two EGFR results, which are based upon MDRD and CKD-EPI formulas.
- CVA or TIA <6 months prior to enrollment
- Patients who are immunosuppressed by medicines (corticosteroids, methotrexate, cyclophosphamide, cyclosporine), illnesses (AIDS, HIV), or neutrophil count <1000/mm3
- Patients receiving other investigational drug therapy within 30 days of enrollment including gene transfer
- Patients with diseases other than CHF that, in the opinion of the investigator, put the subject at risk or adversely affect the results
Contacts and Locations| Contact: H. Kirk Hammond, MD | 858-642-3542 | khammond@ucsd.edu |
| Contact: Eileen M D'Souza | 858-642-3542 | edsouza@vapop.ucsd.edu |
| United States, California | |
| Cedar-Sinai Medical Center | Recruiting |
| Beverly Hills, California, United States, 90211 | |
| Contact: Michelle Kittleson, MD 310-248-8300 michelle.kittleson@cshs.org | |
| Contact: Maria M Thottam, BS, CCRP 310-248-7136 maria.thottam@cshs.org | |
| Principal Investigator: Michelle Kettleson, MD | |
| Sub-Investigator: Jon Kobashigawa, MD | |
| Sub-Investigator: Jignesh Patel, MD | |
| Sub-Investigator: Michele Hamilton, MD | |
| Sub-Investigator: Jaime Moriguchi, MD | |
| Sub-Investigator: Lawrence Czer, MD | |
| Sub-Investigator: David Chang, MD | |
| Sub-Investigator: Antoine Hage, MD | |
| Sub-Investigator: Babak Azarbal, MD | |
| VA San Diego Healthcare System | Recruiting |
| San Diego, California, United States, 92161 | |
| Contact: William Penny, MD 858-642-1129 wpenny@ucsd.edu | |
| Contact: Tiffany M Hancock 858-642-1129 tiffany.hancock@va.gov | |
| Sub-Investigator: Alan Maisel, MD | |
| Sub-Investigator: Denise Barnard, MD | |
| Sub-Investigator: Dan Blanchard, MD | |
| Sub-Investigator: Robert S Ross, MD | |
| United States, Illinois | |
| Northwestern University Feinberg School of Medicine | Recruiting |
| Chicago, Illinois, United States, 60611 | |
| Contact: Clyde W Yancy, MD 312-926-2492 cyancy@nmff.org | |
| Contact: Daniel Roshevsky, CCRC 312-695-3264 droshevs@nmh.org | |
| Principal Investigator: Clyde W Yancy, MD | |
| Sub-Investigator: Ranya Sweis, MD | |
| Sub-Investigator: Keith Benzuly, MD | |
| Sub-Investigator: James Flaherty, MD | |
| Sub-Investigator: Robert Gordon, MD | |
| United States, Minnesota | |
| Minneapolis Heart Institute Foundation | Recruiting |
| Minneapolis, Minnesota, United States, 55407 | |
| Contact: Timothy D Henry, MD 612-863-7372 henry003@umn.edu | |
| Contact: Kathy Beattie, RN,BSN,CCRC 612-863-6289 kathy.beattie@allina.com | |
| Principal Investigator: Timothy D Henry, MD | |
| United States, Vermont | |
| Fletcher Allen Health Care | Recruiting |
| Burlington, Vermont, United States, 05401 | |
| Contact: Matthew W Watkins, MD 802-847-3734 matthew.watkins@vtmednet.org | |
| Contact: Linda Chadwick, RN 802-847-4744 linda.chadwick@vtmednet.org | |
| Principal Investigator: Matthew W Watkins, MD | |
| Sub-Investigator: Martin M LeWinter, MD | |
| Sub-Investigator: Peter C VanBuren, MD | |
| Sub-Investigator: David J Coyle, MD | |
| Sub-Investigator: Enkhtuyaa L Mueller, MD | |
| Sub-Investigator: Cameron W Donaldson, MD | |
| Sub-Investigator: Magdalena A Zeglin-Sawczuk, MD | |
| Study Director: | H. Kirk Hammond, MD | UCSD; VA San Diego Healthcare System; Veterans Medical Research Foundation |
| Principal Investigator: | William Penny, MD | UCSD; VA San Diego Healthcare System; Veteran's Medical Research Foundation |
| Principal Investigator: | Timothy D Henry, MD | Minneapolis Heart Institute Foundation |
| Principal Investigator: | Clyde W Yancy, MD | Bluhm Cardiovascular Institute, Northwestern Memorial Hospital |
| Principal Investigator: | Michelle Kittleson, MD | Cedar-Sinai Medical Center |
| Principal Investigator: | Matthew Watkins, MD | Fletcher Allen Health Care, University of Vermont |
More Information
No publications provided
| Responsible Party: | H Kirk Hammond, MD, Sponsor; UCSD; VA San Diego; Veterans Medical Research Foundation (VMRF), Veterans Medical Research Foundation |
| ClinicalTrials.gov Identifier: | NCT00787059 History of Changes |
| Other Study ID Numbers: | 365, P01HL066941 |
| Study First Received: | November 6, 2008 |
| Last Updated: | November 16, 2012 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Veterans Medical Research Foundation:
|
Adenylyl Cyclase AC6 adenovirus gene therapy |
congestive heart failure intracoronary nitroprusside |
Additional relevant MeSH terms:
|
Heart Failure Heart Diseases Cardiovascular Diseases |
ClinicalTrials.gov processed this record on May 21, 2013