Safety of and Immune Response to a Modified Vaccinia Ankara (MVA) HIV Vaccine in HIV Uninfected Adults

HIV Infections Clinical Trial

Official title:

A Phase I Double-Blind, Randomized, Dose Escalating, Placebo-Controlled, Study of Safety and Immunogenicity of WRAIR/NIH Live Recombinant MVA-CMDR (HIV-1 CM235 Env/ CM240 Gag/Pol) Administered by Intramuscular (IM) or Intradermal (ID) Route In HIV-Uninfected Adults

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00376090
• Other study ID #: RV 158
• Secondary ID: A-12403WRAIR 114
• Status: Completed
• Phase: Phase 1
• First received: September 13, 2006
• Last updated: October 13, 2017
• Start date: July 2005
• Est. completion date: December 2008

Study information

• Verified date: October 2017
• Source: U.S. Army Medical Research and Materiel Command
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine the safety and the immune responses to the HIV vaccine candidate, MVA-CMDR. This vaccine was designed to induce immune responses to three HIV "passenger" genes encoded with the viral vector, MVA.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 48
• Est. completion date: December 2008
• Est. primary completion date: December 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

A participant must meet all of the following criteria:

• Low risk for HIV infection

• 18 to 40 years at the time of enrollment and vaccinia naive

• Good health

• Availability for 12 months of participation.

• Successful completion of the Test of Understanding

• Able and willing to give informed consent.

• HEMATOCRIT: WOMEN: 35 %-45 %; MEN 36 % - 49 %

• White cell count: 3,000 - 11,000 cells/mm3

• Platelets: 125,000 - 450,000 per mm3

• Normal cardiac enzyme level at second Screening Visit

• Urinalysis (UA) for protein and blood: negative or trace.

• Normal liver function tests to include ALT/AST, alkaline phosphatase, GGT (< 1.25x institutional upper limits of normal) and CPK (< 480) and creatinine (< 1.25 mg/dL)

• Negative serology for HIV infection

• Any female volunteer must have a negative serum or urine pregnancy test at the screening visit as well as immediately prior to each vaccine/placebo vaccination, as well as verbal assurance that adequate birth control measures have been followed for 60 days prior to the first vaccine/placebo vaccination and will continue to be followed for at least 3months after the final vaccine/placebo vaccination. This means using any of the following methods: Birth control drugs that prevent pregnancy given by pills, shots or placed under the skin, Male or female condoms with or without a cream or gel that kills sperm, diaphragm or cervical cap with a cream or gel that kills sperm, or Abstinence

Exclusion Criteria:

A volunteer will be excluded if one or more of the following conditions apply.

A woman who:

• Is pregnant.

• Is breast-feeding.

Anyone who:

• Is U.S. military personnel.

• Acknowledges engaging in highest-risk behavior within six months of study entry

• Has active tuberculosis or other systemic infectious process by review of systems and physical examination.

• Has history of or known cardiac disease including any of the following: prior myocardial infarction (heart attack), angina pectoris, congestive heart failure, conduction disturbances, repolarization (ST segment or T wave) abnormalities, serious cardiac arrhythmias (ventricular tachycardia or ventricular fibrillation), cardiomyopathy, pericarditis, stroke or transient ischemic attack, chest pain or shortness of breath with activity (e.g. climbing stairs), valvular heart disease including mitral valve prolapse, or other heart conditions under the care of a doctor.

• Has ECG on Screening Visit 2 with clinical significant findings, or features that would interfere with the assessment of myo/pericarditis (as determined by the contract ECG Lab) including any of the following: conduction disturbance (atrioventricular or intraventricular condition, left or right bundle branch block, AB block of any degree or QTc prolongation), repolarization (ST segment or T wave) abnormality, significant atrial or ventricular arrhythmia, frequent atrial or ventricular ectopy (e.g. frequent premature atrial contractions, 2 premature ventricular contractions in a row), ST elevation consistent with ischemia, or evidence of past or evolving myocardial infarction

• Has history of seizure disorder, immunodeficiency, chronic illness, autoimmune disease, diabetes mellitus active malignancy or use of immunosuppressive medications.

• Has evidence of psychiatric, medical and/or substance abuse problems during the past six months that the investigator believes would adversely affect the volunteer's ability to participate in the trial.

• Has occupational or other responsibilities that would prevent completion of participation in the study.

• Has received any live attenuated vaccine within 60 days of study entry.

• Has used experimental therapeutic agents within 30 days of study entry.

• Has received blood products or immunoglobulins in the past three months.

• Has history of anaphylaxis or other serious adverse reactions to vaccines.

• Has previously received an HIV vaccine or an MVA or vaccinia vaccine.

• Has chronic or active Hepatitis B or Hepatitis C virus infection or active syphilis (positive RPR and FTA).

• Has had an immediate type hypersensitivity reaction to eggs, egg products or neomycin/streptomycin (used to prepare MVA vaccine).

• Is a study site employee.

Related Conditions & MeSH terms

• HIV Infections

Intervention

Biological:
• MVA-CMDR
10^7 PFU IM, 1.0 mL
• Placebo
1.0 mL IM
• MVA-CMDR
10^6 PFU ID, 0.1 mL
• Placebo
0.1 mL ID
• MVA-CMDR
10^8 PFU IM, 1.0 mL
• MVA-CMDR
10^7 PFD ID, 0.1 mL

Locations

Country	Name	City	State
United States	US Military HIV Research Program	Rockville	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
U.S. Army Medical Research and Materiel Command

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety and Tolerability	Evaluate the safety and tolerability of MVA-CMDR (HIV-1 CM235 Env/CM240 Gag/Pol) administered by IM or ID injection to HIV uninfected adults	Study Day 0 through 8 months post-vaccination
Secondary	Immunogenicity	Evaluate the ability of MVA-CMDR (HIV-1 CM235 Env/CM240 Gag/Pol) to induce HIV antigen specific cellular and humoral immune responses	Study Day 0 through Study Day 280