Safety Study of a Human Metapneumovirus Challenge Virus in Healthy Adults
NCT01109329 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 21
Last updated 2013-01-03
Summary
Human metapneumovirus (HMPV) is a virus that can cause respiratory illness. In older adults, those with asthma, infants, and children, illness can be severe, but in healthy adults the virus frequently causes no symptoms. The National Institute of Allergy and Infectious Diseases (NIAID) is working to develop a vaccine for HMPV that could be given to infants. Before potential vaccines can be tested, information about how HMPV affects healthy adults is needed. This study will examine the effects of exposure to HMPV in healthy adults.
Conditions
- Human Metapneumovirus
Interventions
- BIOLOGICAL
-
HMPV challenge virus
Single dose of 10\^6 plaque forming units (PFU) of recombinant HMPV small hydrophobic genes (rHMPV-SHs)
Sponsors & Collaborators
-
National Institute of Allergy and Infectious Diseases (NIAID)
lead NIH
Principal Investigators
-
Ruth Karron, MD · Johns Hopkins University, Bloomberg School of Public Health
Study Design
- Allocation
- NA
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 49 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2010-06-30
- Primary Completion
- 2010-12-31
- Completion
- 2010-12-31
Countries
- United States
Study Locations
More Related Trials
-
Inpatient Challenge Study of rRSV A/Maryland/001/11, a Human Respiratory Syncytial Virus Challenge Strain, Administered to Healthy Adult Volunteers
NCT03624790 ·Status: COMPLETED ·Phase: PHASE1
-
Antiviral Activity, Clinical Outcomes, Safety, Tolerability, and Pharmacokinetics of Oral Lumicitabine Regimens in Hospitalized Adult Participants Infected With Human Metapneumovirus
NCT03502694 ·Status: WITHDRAWN ·Phase: PHASE2
-
RSV Challenge in Healthy Adults
NCT00100373 ·Status: COMPLETED ·Phase: NA
-
MEDI-557 Adult Dosing
NCT01562938 ·Status: COMPLETED ·Phase: PHASE1
-
Intranasal Challenge of Healthy Adults With Respiratory Syncytial Virus (RSV)
NCT01475305 ·Status: TERMINATED ·Phase: PHASE1
-
Safety and Immunogenicity of mRNA-1653, a Combined Human Metapneumovirus (hMPV) and Parainfluenza Virus Type 3 (PIV3) Vaccine, in Healthy Adults, and Children 12 to 59 Months of Age With Serologic Evidence of Prior Exposure
NCT04144348 ·Status: COMPLETED ·Phase: PHASE1
-
Study of a Human Metapneumovirus/Respiratory Syncytial Virus mRNA Vaccine Candidate Encapsulated in a Lipid Nanoparticle-based Formulation in Adults Aged 60 Years and Older
NCT06686654 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1/PHASE2
-
Study of a Respiratory Syncytial Virus/Human Metapneumovirus Vaccine Candidate
NCT06134648 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Study on the Safety and Immunogenicity of Influenza, Respiratory Syncytial Virus, Human Metapneumovirus and Parainfluenza Vaccines in Adults 18 to 49 Years of Age.
NCT06850051 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Safety and Ability of the Vaccine to Induce Antibodies Against the Respiratory Syncytial Virus in Healthy Adults
NCT02298179 ·Status: COMPLETED ·Phase: PHASE1
-
Challenge Infection of Healthy Adult Volunteers With RSV A2
NCT03388645 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Evaluate the Human Infection of the Lower Respiratory Tract in Children at High Risk
NCT00192439 ·Status: COMPLETED
-
Safety Study of Anti-Influenza Virus Monoclonal Antibody to Treat Influenza
NCT01390025 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluating the Safety and Immune Response to a Respiratory Syncytial Virus (RSV) Vaccine in Adults, RSV-Seropositive Children, and RSV-Seronegative Infants and Children
NCT01459198 ·Status: COMPLETED ·Phase: PHASE1
-
Safety of and Immune Response to Recombinant Live Attenuated Parainfluenza Type 3 Virus Vaccine in Healthy Infants and Children
NCT01021397 ·Status: COMPLETED ·Phase: PHASE1
-
Intranasal AD4-H5-VTN as an Adenovirus Vaccine
NCT01806909 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase I, Randomized, Double-Blind, Single-Dose, Dose Escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI-557
NCT00578682 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Learn About New COVD-19 RNA Vaccine Candidates for New Variants in Healthy Individuals
NCT05997290 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
The Development of a Human Model of Respiratory Syncytial Virus Infection
NCT01349543 ·Status: COMPLETED ·Phase: NA
-
Safety, Reactogenicity, and Immunogenicity of mRNA-1653 in Healthy Adults
NCT03392389 ·Status: COMPLETED ·Phase: PHASE1
-
A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate Safety of MEDI-559 in Healthy 1 to <24 Month-Old Children
NCT00767416 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Study to Describe the Safety and Immunogenicity of a RSV Vaccine in Healthy Adults
NCT03529773 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Investigate the Immunogenicity and Safety of mRNA-1345 Vaccine Targeting Respiratory Syncytial Virus (RSV) in High-risk Adults
NCT06067230 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
A Phase 1b/2a Randomized, Double-Blind, Placebo-controlled, Dose-escalation Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI8897, a Monoclonal Antibody With an Extended Half-life Against Respiratory Syncytial Virus, in Healthy Preterm Infants
NCT02290340 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Safety, Tolerability and Immunogenicity of Ad26.RSV.FA2 Followed by Ad35.RSV.FA2 in Healthy Adult Volunteers
NCT02561871 ·Status: COMPLETED ·Phase: PHASE1