- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT00945893
A Study to Evaluate the Safety of H1N1 Monovalent Vaccine (MEDI3414) in Healthy Adults (MI-CP215)
6 september 2011 uppdaterad av: MedImmune LLC
A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety of MEDI3414 in Adults
The purpose of this study was to determine the safety and descriptive immunogenicity of the H1N1 influenza vaccine in healthy adults.
Studieöversikt
Status
Avslutad
Betingelser
Intervention / Behandling
Detaljerad beskrivning
The primary objective of this study was to assess the safety and descriptive immunogenicity of a monovalent influenza virus vaccine containing a new 6:2 influenza virus reassortant in healthy adults.
Studietyp
Interventionell
Inskrivning (Faktisk)
300
Fas
- Fas 4
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Florida
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Daytona Beach, Florida, Förenta staterna, 30060
- Covance Daytona Beach
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Miami, Florida, Förenta staterna, 33126
- Pharmax Research Clinic
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South Miami, Florida, Förenta staterna, 33143
- Miami Research Associates
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Missouri
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Kansas City, Missouri, Förenta staterna, 64114
- Center for Pharmaceutical Research
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Tennessee
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Nashville, Tennessee, Förenta staterna, 37203
- Clinical Research Associates, Inc.
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Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år till 49 år (Vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Male or female, 18 to 49 years of age (not yet reached their 50th birthday) at the time of randomization
- Healthy by medical history and physical examination
- Written informed consent and any locally required authorization (eg, Health Insurance Portability and Accountability Act [HIPAA] in the United States of America [USA], European Union [EU] Data Privacy Directive in the EU) obtained from the subject/legal representative prior to performing any protocol-related procedures, including screening evaluations
- Females of childbearing potential, (ie, unless surgically sterile [eg, bilateral tubal ligation, bilateral oophorectomy, or hysterectomy], has sterile male partner, is at least 1 year post menopause, or practices abstinence) must use an effective method of avoiding pregnancy (including oral, transdermal, or implanted contraceptives, intrauterine device, female condom with spermicide, diaphragm with spermicide, cervical cap, or use of a condom with spermicide by the sexual partner) for 30 days prior to the first dose of investigational product, and must agree to continue using such precautions for 60 days after the second dose of investigational product. In addition, the subject must also have a negative urine or blood pregnancy test at screening and, if screening and Day 1 do not occur on the same day, on the day of vaccination prior to randomization.
- Males, unless not sexually active, must use an effective method of birth control with a female partner and must agree to continue using such contraceptive precautions for at least 30 days after the second dose of investigational product (from Day 1 through Day 59 of the study)
- Subject is available by telephone
- Subject is able to understand and comply with the requirements of the protocol, as judged by the investigator
- Subject is able to complete follow-up period of 180 days after Dose 2 as required by the protocol
Exclusion Criteria:
- History of hypersensitivity to any component of the investigational product including egg or egg protein, gelatin or arginine, or serious, life-threatening, or severe reactions to previous influenza vaccinations
- History of hypersensitivity to gentamicin
- Any condition for which the inactivated influenza vaccine is indicated, including chronic disorders of the pulmonary or cardiovascular systems (eg, asthma), chronic metabolic diseases (eg, diabetes mellitus), renal dysfunction, or hemoglobinopathies that required regular medical follow-up or hospitalization during the preceding year
- Acute febrile (> 100.0°F oral or equivalent) and/or clinically significant respiratory illness (eg, cough or sore throat) within 14 days prior to randomization
- History of asthma
- Any known immunosuppressive condition or immune deficiency disease, including human immunodeficiency virus infection, or ongoing immunosuppressive therapy
- History of Guillain-Barré syndrome
- A household contact who is severely immunocompromised (eg, hematopoietic stem cell transplant recipient, during those periods in which the immunocompromised individual requires care in a protective environment); subject should additionally avoid close contact with severely immunocompromised individuals for at least 21 days after receipt of investigational product
- Receipt of any investigational agent within 30 days prior to randomization, or expected receipt through 30 days after the second dose of investigational product (use of licensed agents for indications not listed in the package insert is permitted)
- Expected receipt of antipyretic or analgesic medication on a daily or every other day basis from randomization through 14 days after receipt of each dose of investigational product
- Administration of intranasal medications within 14 days prior to randomization, or expected receipt through 14 days after administration of each dose of investigational product
- Receipt of any nonstudy vaccine within 30 days before or after Dose 1 or expected receipt of any nonstudy vaccine within 30 days before or after Dose 2
- Known or suspected mitochondrial encephalomyopathy
- Subject is pregnant or a nursing mother
- Any condition (eg, chronic cough, allergic rhinitis) that, in the opinion of the investigator, would interfere with evaluation of the investigational product or interpretation of subject safety or study results
- Subject or immediate family member of subject is an employee of the clinical study site or is otherwise in involved with the conduct of the study
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Fyrdubbla
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: MEDI3414 [Influenza A (H1N1) vaccine]
MEDI3414 - Monovalent vaccine was supplied in intranasal sprayers containing a total volume of 0.5mL of sucrose-phosphate buffer, egg allantoic fluid, and approximately 10^7 fluorescent focus units (FFU) of live, attenuated influenza virus reassortant A/California/7/2009 strain that was propagated in chicken eggs.
H1N1 monovalent influenza vaccine (MEDI3414) contained no preservatives and no adjuvants.
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0.5 mL; (intranasal sprayer)
Andra namn:
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Placebo-jämförare: Placebo
Placebo -Placebo was supplied in intranasal sprayers containing 0.5 mL of sucrose-phosphate buffer.
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(intranasal sprayers containing 0.5 mL of sucrose-phosphate buffer)
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Number of Participants With Fever Post Dose 1 (Days 1-8), Defined as an Oral Temperature ≥ 101°F (38.3°C).
Tidsram: Days 1-8
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The number of participants with fever between the two treatment groups was compared based on the upper limit of the two-sided 95% exact confidence intervals (CIs) for the rate difference (Vaccine minus Placebo).
The upper limit of the two-sided 95% CI was evaluated against the prespecified equivalence criterion of 10% which corresponded to the following hypotheses • H0 (null): rate difference ≥ 10% • HA (alternative): rate difference < 10%
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Days 1-8
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Number of Participants Who Experienced a Post Dose 1 (Day 15) Seroresponse Against the H1N1 Strain in All Participants Regardless of Baseline Serostatus
Tidsram: Day 1, Day 15
|
Seroresponse was defined as a ≥ 4-fold rise in hemagglutination inhibition (HAI) titer from baseline.
All immunogenicity analyses were based on the immunogenicity population.
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Day 1, Day 15
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Number of Participants Who Experienced a Post Dose 1 (Day 29) Seroresponse Against the H1N1 Strain in All Participants Regardless of Baseline Serostatus
Tidsram: Day 1, Day 29
|
Seroresponse was defined as a ≥ 4-fold rise in HAI titer from baseline.
All immunogenicity analyses were based on the immunogenicity population.
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Day 1, Day 29
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Number of Participants Who Experienced a Post Dose 2 (Day 57) Seroresponse Against the H1N1 Strain in All Participants Regardless of Baseline Serostatus
Tidsram: Day 1, Day 57
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Seroresponse was defined as a ≥ 4-fold rise in HAI titer from baseline.
All immunogenicity analyses were based on the immunogenicity population.
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Day 1, Day 57
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Number of Participants With Any Solicited Symptom Within 7 Days Post Vaccination, Dose 1
Tidsram: Days 1-8
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Solicited symptoms were events considered likely to occur post dosing.
For this study, other solicited symptoms included: Fever (> 100°F [37.8°C] oral), Runny nose, Sore throat, Cough, Vomiting, Muscle aches, Chills, Decreased activity (tiredness), and Headache.
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Days 1-8
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Number of Participants Reporting Adverse Events (AEs) Within 7 Days Post Vaccination, Dose 1
Tidsram: Days 1-8
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Days 1-8
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Number of Participants Using Anti-pyretic and Analgesic Agents Within 7 Days Post Vaccination, Dose 1.
Tidsram: Days 1-8
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Days 1-8
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Number of Participants With Any Solicited Symptom Within 14 Days Post Vaccination, Dose 1
Tidsram: Days 1-15
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Days 1-15
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Number of Participants Reporting AEs Within 14 Days Post Vaccination, Dose 1
Tidsram: Days 1-15
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Days 1-15
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Number of Participant Using Anti-pyretic and Analgesic Agents Within 14 Days Post Vaccination, Dose 1
Tidsram: Days 1-15
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Days 1-15
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Number of Participants With Any Solicited Symptom Within 7 Days Post Vaccination, Dose 2
Tidsram: Days 29-36
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Days 29-36
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Number of Participants Reporting AEs Within 7 Days Post Vaccination, Dose 2
Tidsram: Days 29-36
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Days 29-36
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Number of Participants Using Anti-pyretic and Analgesic Agents Within 7 Days Post Vaccination, Dose 2
Tidsram: Days 29-36
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Days 29-36
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Number of Participants With Any Solicited Symptom Within 14 Days Post Vaccination, Dose 2
Tidsram: Days 29-43
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Days 29-43
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Number of Participants Reporting AEs Within 14 Days Post Vaccination, Dose 2
Tidsram: Days 29-43
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Days 29-43
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Number of Participants Using Anti-pyretic and Analgesic Agents Within 14 Days Post Vaccination, Dose 2
Tidsram: Days 29-43
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Days 29-43
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Number of Participants With Serious Adverse Events (SAEs) Through 28 Days Post Vaccination, Dose 1
Tidsram: Days 1-29
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SAEs were those AEs that resulted in death; were immediately life threatening; resulted in inpatient hospitalization or prolongation of existing hospitalization; resulted in persistent or significant disability or incapacity; were a birth defect in the offspring of a participant; or were an important medical event that may not have resulted in death, threatened life, or required hospitalization and that, based on appropriate medical judgment, may have jeopardized the participant and may have required medical or surgical intervention to prevent one of the outcomes listed above.
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Days 1-29
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Number of Participants With New Onset Chronic Diseases (NOCDs) Within 28 Days Post Vaccination, Dose 1
Tidsram: Days 1-29
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An NOCD was a newly diagnosed medical condition that was of a chronic, ongoing nature and was assessed by the investigator as medically significant.
Examples of NOCDs included, but were not limited to, diabetes, asthma, autoimmune disease (eg, lupus, rheumatoid arthritis), and neurological disease (eg, epilepsy, autism).
Examples of events not considered NOCDs were mild eczema, diagnosis of a congenital anomaly present at study entry, or acute illness (eg, otitis media, bronchitis).
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Days 1-29
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Number of Participants With SAEs Through 28 Days Post Vaccination, Dose 2
Tidsram: Days 29-57
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SAEs were those AEs that resulted in death; were immediately life threatening; resulted in inpatient hospitalization or prolongation of existing hospitalization; resulted in persistent or significant disability or incapacity; were a birth defect in the offspring of a participant; or were an important medical event that may not have resulted in death, threatened life, or required hospitalization and that, based on appropriate medical judgment, may have jeopardized the participant and may have required medical or surgical intervention to prevent one of the outcomes listed above.
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Days 29-57
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Number of Participants With NOCDs Within 28 Days Post Vaccination, Dose 2
Tidsram: Days 29-57
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An NOCD was a newly diagnosed medical condition that was of a chronic, ongoing nature and was assessed by the investigator as medically significant.
Examples of NOCDs included, but were not limited to, diabetes, asthma, autoimmune disease (eg, lupus, rheumatoid arthritis), and neurological disease (eg, epilepsy, autism).
Examples of events not considered NOCDs were mild eczema, diagnosis of a congenital anomaly present at study entry, or acute illness (eg, otitis media, bronchitis).
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Days 29-57
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Number of Participants With SAEs Through 180 Days Post Final Dose
Tidsram: Days 1-209
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SAEs were those AEs that resulted in death; were immediately life threatening; resulted in inpatient hospitalization or prolongation of existing hospitalization; resulted in persistent or significant disability or incapacity; were a birth defect in the offspring of a participant; or were an important medical event that may not have resulted in death, threatened life, or required hospitalization and that, based on appropriate medical judgment, may have jeopardized the participant and may have required medical or surgical intervention to prevent one of the outcomes listed above.
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Days 1-209
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Number of Participants With NOCDs Through 180 Days Post Final Dose.
Tidsram: Days 1-209
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An NOCD was a newly diagnosed medical condition that was of a chronic, ongoing nature and was assessed by the investigator as medically significant.
Examples of NOCDs included, but were not limited to, diabetes, asthma, autoimmune disease (eg, lupus, rheumatoid arthritis), and neurological disease (eg, epilepsy, autism).
Examples of events not considered NOCDs were mild eczema, diagnosis of a congenital anomaly present at study entry, or acute illness (eg, otitis media, bronchitis).
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Days 1-209
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Number of Participants Who Achieved a Post Dose 1 (Day 15) HAI Titer ≥ 32 Against the H1N1 Strain in All Participants Regardless of Baseline Serostatus
Tidsram: Day 1, Day 15
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All immunogenicity analyses are based on the immunogenicity population.
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Day 1, Day 15
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Number of Participants Who Achieved a Post Dose 1 (Day 29) HAI Titer ≥ 32 Against the H1N1 Strain in All Subjects Regardless of Baseline Serostatus
Tidsram: Day 1, Day 29
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All immunogenicity analyses are based on the immunogenicity population.
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Day 1, Day 29
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Number of Participants Who Achieved a Post Dose 2 (Day 57) HAI Titer ≥ 32 Against the H1N1 Strain in All Participants Regardless of Baseline Serostatus
Tidsram: Day 1, Day 57
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All immunogenicity analyses are based on the immunogenicity population.
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Day 1, Day 57
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Serum HAI Geometric Mean Titers (GMTs) in All Participants Regardless of Baseline Serostatus, Dose 1 (Day 15)
Tidsram: Day 1, Day 15
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All immunogenicity analyses are based on the immunogenicity population.
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Day 1, Day 15
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Serum HAI GMTs in All Participants Regardless of Baseline Serostatus, Dose 1 (Day 29)
Tidsram: Day 1, Day 29
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All immunogenicity analyses are based on the immunogenicity population.
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Day 1, Day 29
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Serum HAI GMTs in All Participants Regardless of Baseline Serostatus, Dose 2 (Day 29)
Tidsram: Day 1, Day 57
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All immunogenicity analyses are based on the immunogenicity population.
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Day 1, Day 57
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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Samarbetspartners
Utredare
- Studierektor: Raburn Mallory, M.D., MedImmune LLC
Publikationer och användbara länkar
Den som ansvarar för att lägga in information om studien tillhandahåller frivilligt dessa publikationer. Dessa kan handla om allt som har med studien att göra.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart
1 augusti 2009
Primärt slutförande (Faktisk)
1 september 2009
Avslutad studie (Faktisk)
1 mars 2010
Studieregistreringsdatum
Först inskickad
23 juli 2009
Först inskickad som uppfyllde QC-kriterierna
23 juli 2009
Första postat (Uppskatta)
24 juli 2009
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
12 september 2011
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
6 september 2011
Senast verifierad
1 september 2011
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- MI-CP215
- HHS/ASPR (Annat bidrag/finansieringsnummer: HHSO100200900002I)
Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .