Vaccine Therapy, Incomplete Freund's Adjuvant, and GM-CSF in Treating Patients With HIV

This study has been completed.
Sponsor:
Collaborator:
Information provided by:
National Institutes of Health Clinical Center (CC)
ClinicalTrials.gov Identifier:
NCT00381875
First received: September 26, 2006
Last updated: May 1, 2012
Last verified: May 2012
  Purpose

RATIONALE: Vaccines made from peptides may help the body build an effective immune response. Incomplete Freund's adjuvant may stimulate the immune system in different ways and may help the vaccine work better. Colony-stimulating factors, such as GM-CSF, may increase the number of immune cells found in bone marrow or peripheral blood. Giving vaccine therapy together with incomplete Freund's adjuvant and GM-CSF may be an effective treatment for patients with HIV.

PURPOSE: This clinical trial is studying how well giving vaccine therapy together with incomplete Freund's adjuvant and GM-CSF works in treating patients with HIV.


Condition Intervention Phase
Nonneoplastic Condition
Biological: E1M184V peptide vaccine
Biological: incomplete Freund's adjuvant
Biological: sargramostim
Other: immunoenzyme technique
Phase 1

Study Type: Interventional
Study Design: Primary Purpose: Treatment
Official Title: A Pilot Study to Investigate the Safety and Immunogenicity of a Peptide Vaccine for HIV Infected HLA-A2 Individuals Designed to Impede the Development of Antiretroviral Resistance

Resource links provided by NLM:


Further study details as provided by National Institutes of Health Clinical Center (CC):

Primary Outcome Measures:
  • Impact of treatment on immune response, in terms of the difference between cytotoxic T-lymphocyte effector frequency, as measured by enzyme-linked immunospot (ELISPOT) at baseline and at week 20 [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Effects of treatment on viral load [ Designated as safety issue: No ]
  • Sequencing of any resultant HIV strains [ Designated as safety issue: No ]
  • CD4 counts for assessment of effects on HIV disease [ Designated as safety issue: No ]

Estimated Enrollment: 40
Study Start Date: July 2006
Study Completion Date: February 2011
Primary Completion Date: February 2011 (Final data collection date for primary outcome measure)
Detailed Description:

OBJECTIVES:

Primary

  • Assess the safety of vaccination comprising E1M184V peptide with incomplete Freund's adjuvant in combination with sargramostim (GM-CSF) in patients with HIV who are HLA-A2 positive.
  • Assess, preliminarily, the ability of E1M184V peptide vaccine to induce a cytotoxic T-cell response, defined by ELISPOT assay, in these patients.

Secondary

  • Explore, preliminarily, the effect of this regimen on HIV viral load and CD4 count in these patients.
  • Explore, preliminarily, the development of lamivudine or emtricitabine resistance in patients who subsequently receive lamivudine or emtricitabine.
  • Explore, preliminarily, the ability of E1M184V peptide vaccine to induce a cytotoxic T-cell response as assessed by HLA-A2 class I tetramers and intracellular interferon gamma production after stimulation with E1M184V.

OUTLINE: This is a pilot study.

Patients receive vaccination comprising E1M184V peptide and incomplete Freund's adjuvant subcutaneously (SC) on day 1 in weeks 0, 4, 8, 12, and 16. Patients also receive sargramostim (GM-CSF) SC immediately after vaccination and once daily on days 1-4. Some patients do not receive GM-CSF after the first 2 doses of vaccine. Treatment continues in the absence of unacceptable toxicity.

Patients undergo blood collection at baseline and at 4, 12, 20, 36, and 52 weeks for biomarker/laboratory analysis. Assays may include immunoenzyme techniques and viral genotyping.

After completion of study treatment, patients are followed periodically for up to 2 years.

PROJECTED ACCRUAL: A total of 40 patients will be accrued for this study.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

DISEASE CHARACTERISTICS:

  • HIV-1 infection confirmed by Western blot and enzyme-linked immunosorbent assay
  • HLA-A2 positive by polymerase chain reaction-sequence specific primers
  • CD4 T-cell count ≥ 300/mm³
  • Must be receiving stable regimen of highly active antiretroviral therapy (HAART) that does not include lamivudine or emtricitabine for ≥ 1 month prior to study entry

    • Patients on HAART, including lamivudine or emtricitabine, for which there is a medically appropriate regimen that does not include lamivudine or emtricitabine, are eligible if willing to change antiretrovirals
  • Viral load < 50 copies/mL for 1 month prior to study entry

PATIENT CHARACTERISTICS:

  • See Disease Characteristics
  • ECOG performance status 0-1
  • Life expectancy ≥ 6 months
  • Hemoglobin ≥ 9 g/dL
  • WBC ≥ 1,000/mm³
  • Absolute neutrophil count ≥ 750/mm³
  • Platelet count ≥ 75,000/mm³
  • PT and PTT ≤ 120% of control unless lupus anticoagulant detected
  • Bilirubin ≤ 1.5 times upper limit of normal (ULN) (≤ 7.5 mg/dL with direct fraction ≤ 0.7 mg/dL if on protease inhibitor therapy or due to Gilbert's syndrome)
  • AST and ALT ≤ 2.5 times ULN
  • Creatinine ≤ 1.5 mg/dL OR creatinine clearance ≥ 60 mL/min
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • No hepatitis B surface antigen (HBsAg) or a prior history of HBsAg while on lamivudine or emtricitabine

    • Prior treatment with tenofovir and currently HBsAg negative allowed
  • No evidence of a severe or life-threatening infection other than HIV within the past 6 months
  • No opportunistic infections requiring systemic therapy within the past month
  • No active malignancy, except for basal cell carcinoma
  • No known hypersensitivity to incomplete Freund's adjuvant or incomplete Freund's adjuvant VG (vegetable-grade), E1M184V peptide, or sargramostim (GM-CSF)
  • No other abnormality that would be scored as ≥ grade 3 toxicity, except any of the following (if asymptomatic):

    • Hyperuricemia of grade 4 (without physiologic consequences)
    • Elevation of lactate dehydrogenase ≥ grade 3
    • Elevation of creatine phosphokinase (CPK) ≥ grade 3
    • Hypophosphatemia ≥ grade 3 (if patient is on tenofovir)
    • Elevation of alkaline phosphate of grade 3
    • Hyperamylasemia of ≥ grade 3 allowed if any of the following criteria are met:

      • Macroamylasemia
      • Lipase ≤ 2 times ULN
    • Lymphopenia grade 3
  • No other condition that, in the opinion of the investigator, would preclude compliance with study requirements

PRIOR CONCURRENT THERAPY:

  • See Disease Characteristics
  • No systemic corticosteroids within the past 3 weeks

    • Concurrent systemic corticosteroids allowed in the short term only
    • Physiologic replacement doses of steroids allowed
  • No prior vaccination with a vaccine that includes all or part of the reverse transcriptase of HIV-1
  • No other concurrent investigational drugs or vaccinations
  • No concurrent lamivudine or emtricitabine
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00381875

Locations
United States, Maryland
Warren Grant Magnuson Clinical Center - NCI Clinical Trials Referral Office
Bethesda, Maryland, United States, 20892-1182
Sponsors and Collaborators
Investigators
Investigator: Kathleen M. Wyvill, BSN, RN NCI - HIV and AIDS Malignancy Branch
  More Information

Additional Information:
No publications provided

ClinicalTrials.gov Identifier: NCT00381875     History of Changes
Other Study ID Numbers: 060211, 06-C-0211, NCI-P6066, NCI-6958, CDR0000495768
Study First Received: September 26, 2006
Last Updated: May 1, 2012
Health Authority: United States: Food and Drug Administration

Keywords provided by National Institutes of Health Clinical Center (CC):
HIV infection

Additional relevant MeSH terms:
Freund's Adjuvant
Adjuvants, Immunologic
Immunologic Factors
Physiological Effects of Drugs
Pharmacologic Actions

ClinicalTrials.gov processed this record on April 17, 2014