Status and phase
Conditions
Treatments
About
Background:
Influenza, also called flu, is a virus. It can cause mild symptoms such as fever, cough, sore throat, and aches. Sometimes, flu can cause serious complications. Researchers want to see how people s immune systems respond to the flu.
Objective:
To find the smallest dose of influenza H10N7 virus that may cause an uncomplicated mild to moderate flu infection in healthy people. This dose will be used in the future to test how well new flu vaccines work.
Eligibility:
Healthy adults age 18-50.
Design:
Participants will be screened with:
Physical exam with vital signs and weight
Medical and medicine review
Blood and urine tests
Electrocardiogram to measure the heart s electrical activity.
Screening tests will be repeated during the study.
Participants will be tested for SARS-CoV-2 and other respiratory infections. For this, a swab will be inserted into the back of the nose.
Participants will be admitted to an isolation room in the Clinical Center. They will stay in the hospital for at least 10 days. They will not have visitors.
Participants may have a heart ultrasound. They may have lung function tests. For this, they will blow into a tube to measure lung capacity.
One dose of the flu virus will be sprayed into participants nostrils. Participants will be monitored 24 hours a day. They will give nasal samples (using nasal washes and brushes) and blood samples almost every day. They will complete surveys about their symptoms.
Participants will be discharged after they have 2 consecutive negative tests for flu.
Participants will have at least 4 follow-up visits: 1 visit every 2 weeks for 8 weeks.
Full description
Study Description:
This is a dose-finding and pathogenicity study following human challenge with a low pathogenicity avian influenza A H10N7. Participants will be inoculated with 1 dose of challenge virus during the study and then followed for a minimum of 9 weeks after inoculation. Progressively increasing doses will be used according to a specific plan until either the maximum dose is reached or at least 60% of participants develop mild to moderate influenza disease (MMID).
Objectives:
Primary Objective:
Secondary Objective:
Exploratory Objective:
Endpoints:
Primary Endpoint:
Secondary Endpoints:
Exploratory Endpoints:
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
An individual must meet all of the following criteria to be eligible for study participation:
Greater than or equal to 18 and less than or equal to 50 years of age.
Able to provide consent.
Agrees to not use tobacco products, marijuana, or vaping products during participation in this study.
Willing to remain in isolation for a minimum of 10 calendar days (or for the duration of viral shedding) and to comply with all study requirements.
A male subject is eligible for the study if he meets one of the following criteria, beginning at least 4 weeks prior to enrollment and continuing until 10 weeks after administration of the human challenge virus and follow-up visit #4:
A female participant is eligible for this study if she is not pregnant or breastfeeding and meets one of the following criteria, beginning at least 4 weeks prior to enrollment and continuing until 10 weeks after administration of the human challenge virus and follow-up visit #4:
Willing to have samples stored for future research.
Human immunodeficiency virus (HIV) uninfected with a negative test within 60 days of inoculation (Day 0).
EXCLUSION CRITERIA:
An individual meeting any of the following criteria will be excluded from study participation:
Has self-reported or medically documented significant medical condition including but not limited to:
Has close or household (i.e., share the same apartment or house) high-risk contacts including but not limited to:
Persons greater than or equal to 65 years of age.
Children less than or equal to 5 years of age.
Residents of nursing homes.
Persons of any age with significant chronic medical conditions such as:
Has a body mass index (BMI) less than or equal to 18.5 or greater than or equal to 35.
Smokes more than 4 cigarettes or other tobacco products on a weekly basis or any type of vaping/e-cigarette use more than 4 times per week.
History of facial reconstructive procedures or nasopharyngeal malformation.
Positive for Hepatitis B or Hepatitis C infections.
Complete blood count (CBC) with differential outside of the NIH Department of Laboratory Medicine (DLM) normal reference range and deemed clinically significant by the PI.
Grade 2 or higher Hemoglobin for female participants or Grade 1 or higher Hemoglobin for male participants.
Chemistries in the acute care, mineral, and/or hepatic panels, and/or any of the following: lactate dehydrogenase (LDH), uric acid, creatine kinase, and total protein outside of the NIH DLM normal reference range and deemed clinically significant by the PI.
Urinalysis outside of the NIH DLM normal reference range and deemed clinically significant by the PI.
Clinically significant abnormality as deemed by the PI on ECG.
Clinically significant abnormality as deemed by the PI on ECHO.
Clinically significant abnormality as deemed by the PI on the PFT and/or spirometry.
Recent acute illness within 1 week of admission to the NIH CC.
Known allergy to any component of the interventional agent.
Known allergy to treatments for influenza (including but not limited to oseltamivir, nonsteroidals).
Known allergy to 2 or more classes of antibiotics (e.g., penicillins, cephalosporins, fluoroquinolones, or glycopeptides).
Receipt of influenza vaccine within 8 weeks prior to enrollment.
Receipt of blood or blood products (including immunoglobulins) within 3 months prior to enrollment.
Receipt of any unlicensed drug within 3 months or 5.5 half-lives (whichever is greater) prior to enrollment.
Receipt of any unlicensed vaccine within 6 months prior to enrollment.
Self-reported or known history of current alcoholism or drug abuse, or positive urine/serum test for drugs of abuse (i.e., amphetamines, cocaine, benzodiazepines, opiates, or metabolites, but not tetrahydrocannabinol or metabolites).
Self-reported or known history of psychiatric or psychological issues deemed by the PI to be a contraindication to protocol participation
Known close contact with anyone known to have influenza in the past 7 days.
Known close contact with anyone known to have COVID-19 in the past 14 days.
History of COVID-19-related complications, including, but not limited to: inpatient hospitalization, required the use of oxygen, and/or on-going sequelae.
Non-English speaking participants.
Any condition that, in the judgment of the PI, is a contraindication to protocol participation or impairs the volunteer s ability to give informed consent.
Primary purpose
Allocation
Interventional model
Masking
200 participants in 1 patient group
Loading...
Central trial contact
Matthew J Memoli, M.D.; Rani S Athota, Ph.D.
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal