- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01155037
Safety of and Immunogenicity to an H1N1 Influenza Vaccine in HIV-infected Adults (VIP-H1N1)
17. juli 2018 oppdatert av: Marilia Santini de Oliveira, Oswaldo Cruz Foundation
Phase 2 Study to Evaluate the Safety of and the Immunogenicity to an Adjuvanted A(H1N1)v Influenza Vaccine in HIV-Infected Adults
This is a randomized, open label, phase II trial to evaluate the safety and immunogenicity of two different schedules of vaccination against influenza A H1N1 in HIV-infected individuals, in which each of the randomized groups will be compared with HIV-negative volunteers vaccinated with the regimen indicated by the Brazilian National Immunization Program.
Will be included in the study HIV-infected patients, stratified by CD4 count (< 200 cells/mm3 or > 200 cells/mm3) at the time of screening for the study, not receiving antiretroviral therapy treatment or receiving stable treatment for at least 8 weeks, with no plans to change over the next 6 months, eligible to receive vaccine against influenza A H1N1.
The control group will be formed by HIV-negative individuals, confirmed by serology performed at screening, eligible to receive vaccine against influenza A H1N1. Patients infected with HIV will receive one of two possible vaccination regimens: 1) 3.75 µg in two applications 21 days apart, 2) 7.5 µg in two applications 21 days apart.
The volunteers in the control group will receive a single application of 3.75 µg dose of the vaccine.
The study's hypotheses are: 1) The vaccine against the H1N1 virus promotes antibody titers above the level specified for protection (seroconversion), being as safe and well tolerated in patients HIV-1 infected as in non HIV-infected volunteers; 2) The proportion of seroconversion for H1N1 virus vaccine at a dose of 3.75 µg in HIV-1-infected patients is similar to the proportion of seroconversion induced by the same vaccine at a dose of 7.5 µg; 3)The proportion of seroconversion with one dose of the vaccine against H1N1 virus is similar to the proportion after the second dose.
Studieoversikt
Status
Fullført
Forhold
Studietype
Intervensjonell
Registrering (Faktiske)
450
Fase
- Fase 2
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Rio de Janeiro, Brasil
- Instituto de Pesquisa Clinica Evandro Chagas (IPEC) - Fiocruz
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 59 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria - for all participants
- Both genders, aged between 18 and 59 years;
- Capacity to give informed consent voluntarily to participate in the study;
- Study participants with reproductive potential (defined as girls after menarche or women who have not reached menopause at least during 24 consecutive months, or who menstruated during the past 24 months, or have not undergone surgical sterilization) must have pregnancy test negative results, in blood or urine, at screening and in the vaccine application days. If they have sexual practices likely to promote pregnancy, the participants must use some form of contraception during the study period. At least one of the following methods MUST be properly used: Condoms (male or female, Hormonal contraceptive.
- Laboratory results in the study screening: hemoglobin > 8.0 g/dL; Direct bilirubin < 2.5 x the upper limit of normal; Alanine aminotransferase, ALT (SGPT) and aspartate aminotransferase, AST (SGOT) < 3 x the upper limit of normal; Platelet count > 100.000/mm3
Inclusion Criteria - unique to the participants with HIV infection:
- HIV-1 infection (as evidenced by rapid HIV testing or ELISA kit approved and confirmed by repeating the ELISA, IFA, Western blot, HIV-1 plasma viral load) at any time before entering the study.
- Without changing the antiretroviral treatment within 8 weeks prior to the screening for the study: If the volunteer is receiving HAART he/she is required to be using the same regimen within at least 8 weeks before screening. Changes in antiretroviral dosage within 8 weeks prior to entering the study are permitted. In addition, the exchange of pharmacological formulation (eg. the conventional formulation for combination formulations) is allowed. If the volunteer is not on regular antiretroviral treatment, he/she should not have received any dose of any antiretroviral within 8 weeks prior to screening, including for the prevention of HIV vertical transmission (previous prophylactic and therapeutic regimens are allowed)
- Without planning to change or start HAART in the next 6 months.
Inclusion criteria - unique to the participants without HIV infection (control group):
- HIV-negative test result documented by rapid test approved in Brazil
- Health professionals with indication of receiving H1N1 virus vaccine
Exclusion Criteria:
- Use of any systemic anticancer or immunomodulator treatment, corticosteroid, experimental vaccines, interleukins, interferons, growth factors or intravenous immunoglobulin (IVIG) within 45 days prior to entry into the study.
- Pregnancy or lactation.
- Allergy and/or sensitivity or any known hypersensitivity to residues present in the vaccine (egg, chicken protein, egg albumin, formaldehyde, gentamicin sulphate and sodium deoxycholate) and/or thimerosal.
- Use of alcohol or addiction or other conditions which in the opinion of the site's investigator, may interfere with compliance to the study requirements.
D5. Serious illness requiring systemic treatment and/or hospitalization within 45 days prior to entry into the study
- Severe febrile illness or acute infection at the time of screening for the study and/or days of vaccination
- Vaccination against seasonal influenza in the last 12 months prior to study entry
- Previous vaccination against influenza A H1N1
- History or family history of Guillain-Barré Syndrome (parents, siblings, half-siblings or children).
- Diagnosis of neurological condition including (but not limited to) the absence of deep tendon reflexes, Achilles and patellar, in both legs (four missing) in the last six months.
- Disproportionate force loss in lower limb(s) compared to the upper limbs in the last six months.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: 3.75 µg of the vaccine on days 0 and 21
Patients infected with HIV will receive 3.75 µg of an adjuvanted A H1N1 vaccine in two applications 21 days apart.
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Patients infected with HIV will receive 3.75 µg of an adjuvanted A H1N1 vaccine in two applications 21 days apart.
Patients infected with HIV will receive 7.5 µg of an adjuvanted A H1N1 vaccine in two applications 21 days apart.
Control group will receive 3.75 µg of an adjuvanted A H1N1 vaccine in one single application.
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Eksperimentell: 7.5 µg of the vaccine on days 0 and 21
Patients infected with HIV will receive 7.5µg of an adjuvanted A H1N1 vaccine in two applications 21 days apart.
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Patients infected with HIV will receive 3.75 µg of an adjuvanted A H1N1 vaccine in two applications 21 days apart.
Patients infected with HIV will receive 7.5 µg of an adjuvanted A H1N1 vaccine in two applications 21 days apart.
Control group will receive 3.75 µg of an adjuvanted A H1N1 vaccine in one single application.
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Aktiv komparator: 3.75 µg of the vaccine on day 0
The volunteers in the control group will receive a single application of 3.75 µg dose of the vaccine.
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Patients infected with HIV will receive 3.75 µg of an adjuvanted A H1N1 vaccine in two applications 21 days apart.
Patients infected with HIV will receive 7.5 µg of an adjuvanted A H1N1 vaccine in two applications 21 days apart.
Control group will receive 3.75 µg of an adjuvanted A H1N1 vaccine in one single application.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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proportions of seroconversion
Tidsramme: 21 days after vaccination regimen
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proportions of seroconversion for influenza A H1N1 in each of the four subsets of HIV-positive patients, and in the control group
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21 days after vaccination regimen
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proportions of seroprotection
Tidsramme: 21 days after vaccination regimen
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proportions of seroprotection for influenza A H1N1 in each of the four subsets of HIV-positive patients and in the control group
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21 days after vaccination regimen
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Safety of the A H1N1 vaccine at two different regimens in HIV-infected adults
Tidsramme: 1 months after vaccination
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Safety and tolerability of the vaccine against H1N1 virus in different doses and administration regimens in IV-infected adults
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1 months after vaccination
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Prevalence of A H1N1 influenza symptomatic disease in the study population
Tidsramme: 12 months after vaccination
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proportions of the vaccine's protective factor against influenza A H1N1 in each of the four subsets of HIV-positive patients and in the control group
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12 months after vaccination
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Persistence of antibodies against H1N1 virus
Tidsramme: 12 months after vaccination
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Evaluate the persistence of antibody titers against H1N1 virus after the vaccine series in HIV-infected patients and control group
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12 months after vaccination
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Changes in HIV viral load and CD4
Tidsramme: 12 months after vaccination
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Assess changes in HIV-1 viral load and CD4+ counts after the vaccine series.
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12 months after vaccination
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Cellular immune responses to H1N1 vaccination in HIV-infected patients
Tidsramme: 12 months after vaccination
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Determine the cellular immune responses and their correlation to the development and magnitude of responses to H1N1 virus, and compare the cellular immune responses
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12 months after vaccination
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Samarbeidspartnere
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. mars 2010
Primær fullføring (Faktiske)
1. mars 2012
Studiet fullført (Faktiske)
1. april 2012
Datoer for studieregistrering
Først innsendt
29. juni 2010
Først innsendt som oppfylte QC-kriteriene
29. juni 2010
Først lagt ut (Anslag)
1. juli 2010
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
18. juli 2018
Siste oppdatering sendt inn som oppfylte QC-kriteriene
17. juli 2018
Sist bekreftet
1. juli 2018
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- RNA-virusinfeksjoner
- Virussykdommer
- Infeksjoner
- Luftveisinfeksjoner
- Sykdommer i luftveiene
- Blodbårne infeksjoner
- Smittsomme sykdommer
- Seksuelt overførbare sykdommer, virale
- Seksuelt overførbare sykdommer
- Lentivirus infeksjoner
- Retroviridae-infeksjoner
- Immunologiske mangelsyndromer
- Sykdommer i immunsystemet
- Orthomyxoviridae-infeksjoner
- HIV-infeksjoner
- Influensa, menneske
- Fysiologiske effekter av legemidler
- Immunologiske faktorer
- Vaksiner
Andre studie-ID-numre
- VIP-H1N1
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .