A Safety and Immunogenicity Study of a Plasmid DNA Prime and MVA Boost Vaccine in HIV-1 Infected Adults on ART

GeoVax

Status and phase: Completed; Phase 1

Conditions: HIV-1 Infection

Treatments: Biological: JS7 plasmid DNA and MVA62B vaccine

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT01378156

GV-TH-01

Details and patient eligibility

About

GV-TH-01 is an open label Phase 1 study of 9 HIV-1 infected adults with suppressed viremia who started anti-retroviral therapy (ART) within 18 months of a negative HIV antibody test. This study has 3 phases. The first phase is the vaccination phase, where patients are vaccinated with pGA2/JS7 (JS7)DNA and MVA62B vaccines on a prime/boost regimen. The second phase of the study is a treatment interruption phase, whereby ART is interrupted for a 12 week period approximately 8 weeks following the last vaccination. The third phase occurs after the 12 week treatment interruption phase and is called the treatment reinstitution phase, because subjects reinstitute ART and are followed for an additional 24 weeks. The primary objective is to evaluate the safety of the vaccines during the three phases of the study. A secondary objective is to evaluate the immunogenicity of the vaccines during the vaccination phase of the study.

Full description

GV-TH-01 is an open label Phase 1 study of 9 HIV-1 infected adults with suppressed viremia who started anti-retroviral therapy (ART) within 18 months of a negative HIV antibody test. This study has 3 phases. The first phase is the vaccination phase, where patients are vaccinated with pGA2/JS7 (JS7)DNA and MVA62B vaccines on a prime/boost regimen at weeks 1 and 9 (JS7 DNA vaccine) and weeks 17 and 25 (MVA62B). Both vaccines express Gag, Pol, and Env. The second phase of the study is a treatment interruption phase, whereby ART is interrupted for a 12 week period approximately 8 weeks following the last vaccination. The third phase occurs after the 12 week treatment interruption phase and is called the treatment reinstitution phase, because subjects reinstitute ART and are followed for an additional 24 weeks. The primary objective is to evaluate the safety of the vaccines during the three phases of the study. A secondary objective is to evaluate the immunogenicity of the vaccines during the vaccination phase of the study.

Enrollment: 9 patients

Sex: All

Ages: 18 to 50 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 18-50 yrs.

• ART started within 18 mo. of last documented negative HIV Ab test, or within 13 mo. of last negative detuned HIV-1 Ab assay, or within 18 mo. of evolution of Western blot from indeterminate to positive in the presence of a positive Ab test

• No changes to ART treatment within 4 wks. of study entry

• Documentation of level of plasma HIV-1 RNA and CD4+ counts prior to ART

• On stable suppressive ART [HIV-1 RNA < 50 copies/mL (PCR) or < 75 copies/mL (bDNA) for at least 6 mo. prior to starting vaccination]

• No history of virologic failure

• CD4+ > 500 cells/µL

• Nadir CD4+ > 350 cells/µL unless measured in the setting of acute infection

• Laboratory values:

  • Hemoglobin ≥ 10g/dL (male) or 9g/dL (women)
  • ANC > 1000 cells/µL
  • ALT, AST ≤ 2.5 ULN
  • Total bilirubin < 1.5 x ULN (≤ 5 x ULN on atazanavir)
  • Fasting glucose ≤ 125 mg/dL
  • Serum creatine < 1.5 x ULN
  • Creatinine clearance ≥ 60 mL/min (Cockcroft-Gault)
  • Serum creatine phosphokinase (CPK) ≤ 1.5 x ULN
  • UA negative for hemoglobin and glucose and no greater than 1+ protein
  • Any abnormalities must be assessed by the investigator as not clinically significant

• ECG without evidence of current or past MI, or ischemic heart disease

• Willing to provide signed informed consent

• Females: a negative serum or urine β-HCG pregnancy test at screening

• Female subjects of reproductive potential who engage in sexual activity that could lead to pregnancy must agree to avoid pregnancy and agree to consistently use contraception for at least 21 days prior to first vaccination until the last protocol visit.

• Male subjects participating in the study must agree to not attempt to impregnate a female, or participate in sperm donation programs

• Males engaging in sexual activity that could lead to pregnancy must use a condom from the date of receipt of the first study vaccine until the last protocol visit

• Agreement to use condoms for protection against HIV-1 transmission throughout the study

• Participants must be willing to comply with all study requirements and expected to be available for the duration of the study

• Participants must be willing to temporarily discontinue antiretroviral therapy for up to 12 wks. post-vaccinations

Exclusion criteria

• Known infection with HIV-1 subtype other than Clade B
• Chemotherapy for active malignancy in the past 12 mo.
• Prior vaccinations with any HIV-1 vaccine
• Prior vaccination against smallpox within the last 15 yrs.
• History of or known cardiac disease
• History of myositis
• Diagnosis of HIV-associated nephropathy
• Evidence of active HBV or HCV infection
• Framingham Global Risk Assessment Score consistent with high short-term (10 yr.) cardiac risk
• Receipt of immunomodulatory agents, systemic corticosteroids (including nonprescription street steroids), gamma globulin, or investigational agents (other than H1N1 influenza vaccine) within 6 mo. of screening
• Any immunization within 1 mo. of screening and within 2 wks. of any inoculation in this study
• Creatine supplements within 14 days of baseline and unwillingness to discontinue use throughout the trial
• Changes in ART regimen prior to entry due to virologic failure (not including toxicity)
• Pregnancy or breastfeeding
• Any clinically significant diseases (other than HIV-1 infection) or clinically significant findings during the screening medical history or physical examination that, in the investigator's opinion, would compromise participant safety
• Active alcohol or substance abuses
• Allergy to chicken egg derived products
• Contraindication to intramuscular injection
• Unwilling to forego vigorous exercise 3 days prior to each vaccination

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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9 participants in 1 patient group

JS7 plasmid DNA and MVA62B vaccines

Experimental group

Description:

All subjects receive JS7 plasmid DNA (at 1 and 9 weeks) and MVA62B vaccines (17 and 25 weeks), followed (in 2 months after last vaccination) by a 12-week treatment interruption phase. Subjects reinstitute therapy after the treatment interruption and are followed for 6 months.

Treatment:

Biological: JS7 plasmid DNA and MVA62B vaccine