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

2013年2月25日 更新者: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.

調査の概要

詳細な説明

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.

研究の種類

介入

入学 (実際)

152

段階

  • フェーズ2
  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Florida
      • Melbourne、Florida、アメリカ、32935
        • Accelovance - Melbourne

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

はい

受講資格のある性別

全て

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:防止
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:トリプル

武器と介入

参加者グループ / アーム
介入・治療
実験的:Fluzone + 0.45 mg LIQ001
Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine) Administered with LIQ001 (0.45mg)
A single vaccination of Fluzone alone
他の名前:
  • seasonal influenza vaccination
  • seasonal influenza vaccine
  • seasonal flu vaccination
  • seasonal flu vaccine
A single vaccination of 0.45 mg LIQ001
実験的:Fluzone + 1.8 mg LIQ001
Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine) Administered with LIQ001 (1.8mg)
A single vaccination of Fluzone alone
他の名前:
  • seasonal influenza vaccination
  • seasonal influenza vaccine
  • seasonal flu vaccination
  • seasonal flu vaccine
A single vaccination of 1.8 mg LIQ001
アクティブコンパレータ:Fluzone
Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine)
A single vaccination of Fluzone alone
他の名前:
  • seasonal influenza vaccination
  • seasonal influenza vaccine
  • seasonal flu vaccination
  • seasonal flu vaccine

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
The rate of Adverse Events attributable to each of the doses of LIQ001 mixed with Fluzone compared to Fluzone alone.
時間枠:35 days post-vaccination
35 days post-vaccination

二次結果の測定

結果測定
時間枠
HAI response (Geometric Mean Titer) of each of the doses of LIQ001 mixed with Fluzone compared to the Fluzone alone response.
時間枠: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.
時間枠: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.
時間枠:21 days post-vaccination
21 days post-vaccination

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • スタディディレクター:Frank Malinoski, MD, PhD、Liquidia Technologies, Inc.

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始

2010年9月1日

一次修了 (実際)

2011年12月1日

研究の完了 (実際)

2011年12月1日

試験登録日

最初に提出

2010年10月14日

QC基準を満たした最初の提出物

2010年10月19日

最初の投稿 (見積もり)

2010年10月20日

学習記録の更新

投稿された最後の更新 (見積もり)

2013年3月1日

QC基準を満たした最後の更新が送信されました

2013年2月25日

最終確認日

2013年2月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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