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

NCT ID: NCT00376090

Last Updated: 2017-10-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-07-31

Study Completion Date

2008-12-31

Brief Summary

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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.

Detailed Description

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Conditions

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HIV Infections

Keywords

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MVA vector Immunogenicity HIV vaccine HIV preventative vaccine

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Group I Vaccine

Group Type EXPERIMENTAL

MVA-CMDR

Intervention Type BIOLOGICAL

10\^7 PFU IM, 1.0 mL

Group I Placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type BIOLOGICAL

1.0 mL IM

Group II Vaccine

Group Type EXPERIMENTAL

MVA-CMDR

Intervention Type BIOLOGICAL

10\^6 PFU ID, 0.1 mL

Group II Placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type BIOLOGICAL

0.1 mL ID

Group III Vaccine

Group Type EXPERIMENTAL

MVA-CMDR

Intervention Type BIOLOGICAL

10\^8 PFU IM, 1.0 mL

Group III Placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type BIOLOGICAL

1.0 mL IM

Group IV Vaccine

Group Type EXPERIMENTAL

MVA-CMDR

Intervention Type BIOLOGICAL

10\^7 PFD ID, 0.1 mL

Group IV Placebo

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type BIOLOGICAL

0.1 mL ID

Interventions

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MVA-CMDR

10\^7 PFU IM, 1.0 mL

Intervention Type BIOLOGICAL

Placebo

1.0 mL IM

Intervention Type BIOLOGICAL

MVA-CMDR

10\^6 PFU ID, 0.1 mL

Intervention Type BIOLOGICAL

Placebo

0.1 mL ID

Intervention Type BIOLOGICAL

MVA-CMDR

10\^8 PFU IM, 1.0 mL

Intervention Type BIOLOGICAL

MVA-CMDR

10\^7 PFD ID, 0.1 mL

Intervention Type BIOLOGICAL

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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U.S. Army Medical Research and Development Command

FED

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mary Marovich, MD, DTM&H

Role: PRINCIPAL_INVESTIGATOR

US Military HIV Research Program

Locations

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US Military HIV Research Program

Rockville, Maryland, United States

Site Status

Countries

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United States

References

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Currier JR, Ngauy V, de Souza MS, Ratto-Kim S, Cox JH, Polonis VR, Earl P, Moss B, Peel S, Slike B, Sriplienchan S, Thongcharoen P, Paris RM, Robb ML, Kim J, Michael NL, Marovich MA. Phase I safety and immunogenicity evaluation of MVA-CMDR, a multigenic, recombinant modified vaccinia Ankara-HIV-1 vaccine candidate. PLoS One. 2010 Nov 15;5(11):e13983. doi: 10.1371/journal.pone.0013983.

Reference Type DERIVED
PMID: 21085591 (View on PubMed)

Other Identifiers

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A-12403

Identifier Type: OTHER

Identifier Source: secondary_id

WRAIR 1143

Identifier Type: OTHER

Identifier Source: secondary_id

RV 158

Identifier Type: -

Identifier Source: org_study_id