이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

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

2013년 2월 25일 업데이트: 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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (실제)

152

단계

  • 2 단계
  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Florida
      • Melbourne, Florida, 미국, 32935
        • Accelovance - Melbourne

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

연구 대상 성별

모두

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 방지
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 삼루타

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Fluzone + 0.45 mg LIQ001
Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine) Administered with LIQ001 (0.45mg)
A single vaccination of Fluzone alone
다른 이름들:
  • seasonal influenza vaccination
  • seasonal influenza vaccine
  • seasonal flu vaccination
  • seasonal flu vaccine
A single vaccination of 0.45 mg LIQ001
실험적: Fluzone + 1.8 mg LIQ001
Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine) Administered with LIQ001 (1.8mg)
A single vaccination of Fluzone alone
다른 이름들:
  • seasonal influenza vaccination
  • seasonal influenza vaccine
  • seasonal flu vaccination
  • seasonal flu vaccine
A single vaccination of 1.8 mg LIQ001
활성 비교기: Fluzone
Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine)
A single vaccination of Fluzone alone
다른 이름들:
  • seasonal influenza vaccination
  • seasonal influenza vaccine
  • seasonal flu vaccination
  • seasonal flu vaccine

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
기간
The rate of Adverse Events attributable to each of the doses of LIQ001 mixed with Fluzone compared to Fluzone alone.
기간: 35 days post-vaccination
35 days post-vaccination

2차 결과 측정

결과 측정
기간
HAI response (Geometric Mean Titer) of each of the doses of LIQ001 mixed with Fluzone compared to the Fluzone alone response.
기간: 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.
기간: 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.
기간: 21 days post-vaccination
21 days post-vaccination

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 책임자: Frank Malinoski, MD, PhD, Liquidia Technologies, Inc.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작

2010년 9월 1일

기본 완료 (실제)

2011년 12월 1일

연구 완료 (실제)

2011년 12월 1일

연구 등록 날짜

최초 제출

2010년 10월 14일

QC 기준을 충족하는 최초 제출

2010년 10월 19일

처음 게시됨 (추정)

2010년 10월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (추정)

2013년 3월 1일

QC 기준을 충족하는 마지막 업데이트 제출

2013년 2월 25일

마지막으로 확인됨

2013년 2월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

Fluzone® (2010/2011 Inactivated Trivalent Influenza Vaccine)에 대한 임상 시험

구독하다