- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00376090
Safety of and Immune Response to a Modified Vaccinia Ankara (MVA) HIV Vaccine in HIV Uninfected Adults
13. oktober 2017 opdateret af: U.S. Army Medical Research and Development Command
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
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.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
48
Fase
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Maryland
-
Rockville, Maryland, Forenede Stater, 20850
- US Military HIV Research Program
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
18 år til 40 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
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.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Group I Vaccine
|
10^7 PFU IM, 1.0 mL
10^6 PFU ID, 0.1 mL
10^8 PFU IM, 1.0 mL
10^7 PFD ID, 0.1 mL
|
|
Placebo komparator: Group I Placebo
|
1.0 mL IM
0.1 mL ID
|
|
Eksperimentel: Group II Vaccine
|
10^7 PFU IM, 1.0 mL
10^6 PFU ID, 0.1 mL
10^8 PFU IM, 1.0 mL
10^7 PFD ID, 0.1 mL
|
|
Placebo komparator: Group II Placebo
|
1.0 mL IM
0.1 mL ID
|
|
Eksperimentel: Group III Vaccine
|
10^7 PFU IM, 1.0 mL
10^6 PFU ID, 0.1 mL
10^8 PFU IM, 1.0 mL
10^7 PFD ID, 0.1 mL
|
|
Placebo komparator: Group III Placebo
|
1.0 mL IM
0.1 mL ID
|
|
Eksperimentel: Group IV Vaccine
|
10^7 PFU IM, 1.0 mL
10^6 PFU ID, 0.1 mL
10^8 PFU IM, 1.0 mL
10^7 PFD ID, 0.1 mL
|
|
Placebo komparator: Group IV Placebo
|
1.0 mL IM
0.1 mL ID
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Safety and Tolerability
Tidsramme: Study Day 0 through 8 months post-vaccination
|
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
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Immunogenicity
Tidsramme: Study Day 0 through Study Day 280
|
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
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Efterforskere
- Ledende efterforsker: Mary Marovich, MD, DTM&H, US Military HIV Research Program
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. juli 2005
Primær færdiggørelse (Faktiske)
1. december 2008
Studieafslutning (Faktiske)
1. december 2008
Datoer for studieregistrering
Først indsendt
13. september 2006
Først indsendt, der opfyldte QC-kriterier
13. september 2006
Først opslået (Skøn)
14. september 2006
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
16. oktober 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
13. oktober 2017
Sidst verificeret
1. oktober 2017
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- RV 158
- A-12403 (Anden identifikator: USAMRMC HSRRB)
- WRAIR 1143 (Anden identifikator: WRAIR HURC)
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .