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Zika Virus Purified Inactivated Vaccine (ZPIV) Accelerated Vaccination Schedule Study (Z001)

22. august 2018 oppdatert av: Kathryn Stephenson

A Phase 1, Randomized, Double-Blind Placebo-Controlled Clinical Trial to Evaluate the Safety and Immunogenicity of an Accelerated Vaccination Schedule With a Zika Virus Purified Inactivated Vaccine Plus Alum Adjuvant in Healthy Adults

This is a phase 1 trial of one or more administrations of Zika Virus Purified Inactivated Vaccine (ZPIV). The trial will be conducted under a placebo controlled, double-blind, randomized allocation of study product. There are four groups in the study. Each group is testing a different vaccine schedule.

Studieoversikt

Status

Fullført

Forhold

Studietype

Intervensjonell

Registrering (Faktiske)

36

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Massachusetts
      • Boston, Massachusetts, Forente stater, 02215
        • Center for Virology and Vaccine Research Clinical Trials Unit, Beth Israel Deaconess Medical Center

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 50 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  1. Age 18-50 years old.
  2. Ability and willingness to provide informed consent.
  3. Assessment of understanding: completion of a questionnaire prior to first screening procedure; verbally demonstrate understanding of all questionnaire items answered incorrectly.
  4. Available for the duration of the trial.
  5. Good general health as shown by medical history, physical exam, and screening laboratory tests.
  6. The following laboratory parameters:

    • Hematology

      • Hemoglobin ≥10.5 g/dL for women; ≥11 g/dL for men
      • Absolute Neutrophil Count (ANC): ≥1000/mm3
      • Platelets: 125,000 to 550,000/mm3
    • Chemistry

      • Creatinine: <1.1 x upper limit of normal (ULN)
      • AST: <1.25 x ULN
      • ALT: <1.25 x ULN
    • Normal urinalysis

      • Negative urine glucose.
      • Negative or trace urine protein.
      • Negative or trace urine hemoglobin (if trace hemoglobin is present on dipstick, a microscopic urinalysis within institutional range).
  7. All female participants must be willing to undergo serum or urine beta human chorionic gonadotropin pregnancy tests at time points indicated in the Schedule of Procedures and must test negative prior to vaccination.
  8. All sexually active males (unless anatomically sterile) must be willing to use an effective method of contraception (such as consistent condom use) from the day of first vaccination until Week 12.
  9. If a woman of child-bearing potential, committed to use an effective method of contraception when sexually active with men until Week 12, including:

    • Condoms (male or female) with or without spermicide.
    • Diaphragm or cervical cap with spermicide.
    • Intrauterine device.
    • Hormonal contraception.
    • Successful vasectomy in the male partner (considered successful if a woman reports that a male partner has [1] documentation of azoospermia by microscopy, or [2] a vasectomy more than 2 years ago with no resultant pregnancy despite sexual activity post-vasectomy).
    • Not be of reproductive potential, such as having undergone hysterectomy, bilateral oophorectomy, or tubal ligation.

Exclusion Criteria:

  1. History of known flavivirus infection or previous receipt of flavivirus vaccine.
  2. Positive serology for HIV-1, Hepatitis B surface antigen, or anti-hepatitis C virus antibodies prior to enrollment.
  3. Planned travel to areas with active Zika virus transmission during the study period.
  4. Recent (within 3 weeks) travel to an area with active Zika virus transmission.
  5. Current or planned participation in another clinical trial of an experimental agent during the study period.
  6. Pregnant or lactating.
  7. Any condition, including any clinically significant acute or chronic medical condition, for which, in the opinion of the investigator, participation would not be in the best interest of the subject (eg, compromise the well-being) or that could prevent, limit, or confound the protocol-specified assessments.
  8. Use of anticancer, antituberculosis or other medications considered significant by the investigator within the previous 6 months.
  9. Receipt of live-attenuated vaccine within the previous 60 days or planned receipt within 60 days after vaccination with Investigational Product (within 14 days for live attenuated influenza vaccine [LAIV]); or receipt of other vaccine (e.g., influenza, pneumococcal), allergy treatment with antigen injections or tuberculin skin test within the previous 14 days or planned receipt within 14 days after vaccination with Investigational Product
  10. Receipt of blood transfusion or blood-derived products within the previous 3 months.
  11. Previous severe local or systemic reactions to vaccination.
  12. History of splenectomy
  13. History of seizure in the last 3 years (participants with a history of seizures who have neither required medications nor had a seizure for 3 years are not excluded)
  14. Known autoimmune disease
  15. Asthma other than mild, well-controlled asthma. Exclude participants who:

    1. Use a bronchodilator (beta 2 agonist) daily, or
    2. In the past year have (any of the following):

    i. Had > 1 exacerbation of symptoms treated with oral steroids ii. Routinely used moderate to high dose inhaled corticosteroids (e.g., more than the equivalent of 250 mcg fluticasone; 400 mcg budesonide; 500 mcg beclomethasone; or 1000 mcg triamcinolone/flunisolide, as a daily dose) or theophylline iii. Needed emergency care, urgent care, hospitalization, or intubation for asthma c. Prophylactic bronchodilator use prior to exercise is not exclusionary

  16. Diabetes mellitus type 1 or type 2, including cases controlled with diet alone. (Not excluded: history of isolated gestational diabetes.)
  17. Thyroidectomy, or thyroid disease requiring medication during the last 12 months
  18. Angioedema within the last 3 years if episodes are considered serious or have required medication within the last 2 years
  19. Uncontrolled Hypertension:

    1. If a person has been diagnosed with hypertension during screening or previously, exclude for hypertension that is not well controlled. Well- controlled hypertension is defined as blood pressure consistently ≤ 140 mm Hg systolic and ≤ 90 mm Hg diastolic, with or without medication, with only isolated, brief instances of higher readings, which must be ≤ 150 mm
    2. If a person has NOT been diagnosed with hypertension during screening or previously, exclude for systolic blood pressure ≥ 150 mm Hg at enrollment or diastolic blood pressure ≥ 90 mm Hg at enrolment
  20. Bleeding disorder diagnosed by a doctor (e.g. factor deficiency, coagulopathy, or platelet disorder requiring special precautions)
  21. Malignancy (Not excluded: a participant with a surgical excision and subsequent observation period that in the investigator's estimation has a reasonable assurance of sustained cure or is unlikely to recur during the study period)
  22. Psychiatric condition that compromises safety of the participant or precludes compliance with the protocol, specifically excluding persons with psychoses within the past 3 years, ongoing risk for suicide, or history of suicide attempt or gesture within the past 3 years

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: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 4 Week Schedule
Zika Purified Inactivated Vaccine 5 mcg (or placebo) IM at Week 0 and Week 4
Eksperimentell: 2 Week Schedule
Zika Purified Inactivated Vaccine 5 mcg (or placebo) IM at Week 0 and Week 2
Eksperimentell: Single Vaccination Schedule
Zika Purified Inactivated Vaccine 5 mcg (or placebo) IM at Week 0 only

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Incidence, intensity, and relationship to vaccination of solicited local and systemic adverse events
Tidsramme: 7 days following each vaccination
7 days following each vaccination
Incidence, intensity, and relationship to vaccination of unsolicited local and systemic adverse events
Tidsramme: 28 days following each vaccination
28 days following each vaccination
Incidence, intensity, and relationship to vaccination of serious local and systemic adverse events
Tidsramme: 365 days following each vaccination
365 days following each vaccination

Sekundære resultatmål

Resultatmål
Tidsramme
ZIKV microneutralization Log10 MN50 titers
Tidsramme: 28 days following last vaccination, and at 6 months
28 days following last vaccination, and at 6 months
Zika Env-specific Log10 endpoint ELISA titers
Tidsramme: 28 days following last vaccination, and at 6 months
28 days following last vaccination, and at 6 months
Zika Plaque reduction neutralization test titer
Tidsramme: 28 days following last vaccination, and at 6 months
28 days following last vaccination, and at 6 months
IFN-γ ELISPOT responses to prM, Env, Cap, and NS1 peptides
Tidsramme: 28 days following last vaccination, and at 6 months
28 days following last vaccination, and at 6 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

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 (Faktiske)

8. desember 2016

Primær fullføring (Faktiske)

4. juni 2018

Studiet fullført (Faktiske)

4. juni 2018

Datoer for studieregistrering

Først innsendt

12. oktober 2016

Først innsendt som oppfylte QC-kriteriene

17. oktober 2016

Først lagt ut (Anslag)

18. oktober 2016

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

23. august 2018

Siste oppdatering sendt inn som oppfylte QC-kriteriene

22. august 2018

Sist bekreftet

1. august 2018

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

UBESLUTTE

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