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A Study Evaluating the Safety and Tolerability of a Seasonal Influenza Vaccine Containing LIQ001 (LIfT)

25. Februar 2013 aktualisiert von: Liquidia Technologies, Inc.

A Randomized, Observer-Blind, Controlled Phase 1/2a Study of the Safety, Tolerability and Immunogenicity of Fluzone Administered With and Without LIQ001 in Two Cohorts of Healthy Subjects: 18-49 Years of Age and 65 Years of Age or Older.

This study is designed to evaluate the safety, tolerability, and immune response of LIQ001 mixed with a commercially available seasonal influenza vaccine (Fluzone) in two populations of subjects; healthy adult subjects 18 to 49 years of age and healthy elderly subjects 65 years of age or older.

Studienübersicht

Detaillierte Beschreibung

Significant advances have been made in the design and delivery of vaccines for the prevention of influenza over the decades. However, two major hurdles remain in the global approach to influenza prevention. First, recent epidemiology research has demonstrated that immune response and protection in elderly populations are suboptimal resulting in significant seasonal influenza disease in this population every year. Second, while preparations for the emergence of pandemic influenza strains have progressed, current egg-based manufacturing methods have not provided sufficient global capacity. Furthermore, the genesis and scale-up of other manufacturing platforms will not rapidly solve this problem. Thus, safe and effective ways are needed to improve protection in the elderly as well as reduce the antigen dose in younger populations in preparation for global needs of pandemic vaccines.

Historically it is known that presentation of antigens in particulate form, for a wide range of pathogens, has clear advantages over the presentation of soluble antigen alone. A novel approach using highly uniform particles has been developed which utilizes size, shape, and composition to control the delivery and presentation of the vaccine antigen(s) to the immune system. Production of these highly uniform particles is possible because of a proprietary manufacturing approach called Pattern Replication in Non-wetting Templates (PRINT®).

The proposed approach is to use the PRINT process to make bioabsorbable particles to improve the immune response and efficacy of the seasonal influenza vaccine. It is proposed that mixing properly sized and charged particles with commercial trivalent influenza vaccine (TIV) will increase vaccine effectiveness and/or decrease the amount of antigen necessary to induce an immune response.

Studientyp

Interventionell

Einschreibung (Tatsächlich)

152

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

    • Florida
      • Melbourne, Florida, Vereinigte Staaten, 32935
        • Accelovance - Melbourne

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre und älter (Erwachsene, Älterer Erwachsener)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Age 18 to 49 years (Cohort 1) and age 65 or above (Cohort 2)
  • For subjects 18 to 49 years of age: in good health as determined by medical history, physical examination, and the clinical judgment of the Principal Investigator (PI)
  • For subjects 65 years of age and older: in stable good health as determined by medical history, physical examination, and the clinical judgment of the PI
  • Live in the community (including assisted living)
  • Available for duration of study (1 year)
  • If female, no child-bearing potential or using appropriate measures to prevent pregnancy
  • Negative urine pregnancy test for women presumed to be of child-bearing potential within 24 hours of vaccination
  • Be eligible for screening
  • Provide informed consent
  • Have working phone for contact by the study site personnel

Exclusion Criteria:

  • Known allergy to eggs or any other component of Fluzone (including natural latex) or inactivated influenza vaccines or the investigational vaccine
  • Received seasonal influenza or H1N1 vaccine in last 6 months
  • A diagnosis of influenza within the previous 12 months
  • Received any licensed vaccine within the past 1 month
  • Receiving nursing home or equivalent care
  • For women, breast-feeding or planning to become pregnant during the first three months post-vaccination
  • Chronic administration of immunosuppressant(s) or other medication that modifies immune function
  • Confirmed immunodeficiency syndrome or disease
  • Significant cardiovascular disease including class 3 or 4 congestive heart failure, recent history (last 6 months) of acute myocardial infarction, coronary artery bypass surgery or stent placement, unstable angina, uncontrolled arrhythmia, and for subjects 65 years of age and older, a resting heart rate greater than 100 bpm
  • Hypertension that is not well controlled by medication in the judgment of the investigator or is more than 150/95 at enrollment
  • Bleeding disorder diagnosed by a doctor or significant bruising or bleeding difficulties with IM injections or blood draws
  • Medically significant chronic lung disease, e.g., requiring chronic steroid treatment (oral doses >10 mg/day)
  • Asthma that is severe, unstable or required emergent care, urgent care, hospitalization or intubation during the past two years or that requires the use of oral, intravenous, or high dose inhaled corticosteroids (mild or intermittent asthma treated with inhaled steroids is acceptable)
  • Medically significant acute or progressive hepatic disease
  • Medically significant acute or progressive renal disease
  • Diabetes mellitus type 2 not under pharmacological control
  • A diagnosis of cancer with active treatment within the previous 5 years (except for a localized basal cell carcinoma of the skin)
  • History of autoimmune/inflammatory conditions (e.g., rheumatoid arthritis and diabetes mellitus type 1)
  • Medically significant acute or progressive neurological disease.
  • Seizure disorder that has required treatment within the last 3 years
  • History of Guillain-Barre Syndrome (GBS)
  • Administration of blood products, immunoglobulin, or investigational vaccine in the 3 months prior to immunization in this study
  • Use of investigational product (other than blood, immunoglobulin, or vaccine) in the past 60 days
  • Seropositive for HCV, HIV or positive for HBsAg
  • History of excessive alcohol use, drug abuse, or significant psychiatric illness
  • Unable to complete informed consent
  • Abnormal laboratory assessment meeting criteria for a mild, moderate, or severe adverse event
  • Any other condition or circumstance which, in the opinion of the PI, poses an unacceptable risk for participation in the study
  • Inability to operate and answer a telephone and lack of access to telephone
  • Temporary Exclusion Criteria: Presence of an oral temperature ≥99.5°F, and/or signs and symptoms of an acute infectious respiratory illness within 3 days prior to vaccination

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Verhütung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Verdreifachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Fluzone + 0.45 mg LIQ001
Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine) Administered with LIQ001 (0.45mg)
A single vaccination of Fluzone alone
Andere Namen:
  • seasonal influenza vaccination
  • seasonal influenza vaccine
  • seasonal flu vaccination
  • seasonal flu vaccine
A single vaccination of 0.45 mg LIQ001
Experimental: Fluzone + 1.8 mg LIQ001
Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine) Administered with LIQ001 (1.8mg)
A single vaccination of Fluzone alone
Andere Namen:
  • seasonal influenza vaccination
  • seasonal influenza vaccine
  • seasonal flu vaccination
  • seasonal flu vaccine
A single vaccination of 1.8 mg LIQ001
Aktiver Komparator: Fluzone
Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine)
A single vaccination of Fluzone alone
Andere Namen:
  • seasonal influenza vaccination
  • seasonal influenza vaccine
  • seasonal flu vaccination
  • seasonal flu vaccine

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
The rate of Adverse Events attributable to each of the doses of LIQ001 mixed with Fluzone compared to Fluzone alone.
Zeitfenster: 35 days post-vaccination
35 days post-vaccination

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
HAI response (Geometric Mean Titer) of each of the doses of LIQ001 mixed with Fluzone compared to the Fluzone alone response.
Zeitfenster: 21 days post-vaccination
21 days post-vaccination
HAI response (Percent with HAI titer greater than or equal to 1:40) of each of the doses of LIQ001 mixed with Fluzone compared to the Fluzone alone response.
Zeitfenster: 21 days post-vaccination
21 days post-vaccination
HAI response (Seroconversion rate) of each of the doses of LIQ001 mixed with Fluzone compared to the Fluzone alone response.
Zeitfenster: 21 days post-vaccination
21 days post-vaccination

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Studienleiter: Frank Malinoski, MD, PhD, Liquidia Technologies, Inc.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. September 2010

Primärer Abschluss (Tatsächlich)

1. Dezember 2011

Studienabschluss (Tatsächlich)

1. Dezember 2011

Studienanmeldedaten

Zuerst eingereicht

14. Oktober 2010

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

19. Oktober 2010

Zuerst gepostet (Schätzen)

20. Oktober 2010

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

1. März 2013

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

25. Februar 2013

Zuletzt verifiziert

1. Februar 2013

Mehr Informationen

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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