Collection of Plasma From People Who Recovered From or Were Vaccinated to Emerging Infectious Diseases
NCT02338986 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 10
Last updated 2025-05-16
Summary
Background:
\- There are more emerging infectious diseases recently. Some could affect many people. Some like Severe Acute Respiratory Syndrome (SARS) or Middle East Respiratory Syndrome (MERS) are caused by new germs. Sometimes known germs suddenly infect new and large areas, like Ebola. Many of these diseases don t have good treatments available. Researchers may be able to develop a treatment by using antibodies against these infections.
Objective:
\- To collect antibodies from people with high levels of antibodies to the diseases being studied.
Eligibility:
\- Ages 18-70 years old who weigh at least 110 pounds. They may have been infected with or vaccinated for one of the new infections researchers are studying.
Design:
* Participants will be screened with medical history and blood tests. Researchers will determine if the participant can have apheresis.
* Participants will have apheresis. First, they will be interviewed. Then, a needle will be placed in a vein. Blood will be drawn, and a machine will separate the blood cells from the antibodies and protein. The blood cells will then be returned to the participant through another vein. It takes about 60 minutes for the actual collection.
* Participants will be asked to have the procedure at least 3 times. They can participate in up to 20 sessions total as part of this study. There must be at least 7 days between sessions.
Conditions
- Communicable Diseases
- Communicable Diseases, Emerging
- Emerging Infectious Diseases
- Infection
Interventions
- DRUG
-
Plasma
Plasma
Sponsors & Collaborators
-
National Institute of Allergy and Infectious Diseases (NIAID)
lead NIH
Principal Investigators
-
Richard T Davey, M.D. · National Institute of Allergy and Infectious Diseases (NIAID)
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2015-03-04
- Primary Completion
- 2025-05-15
- Completion
- 2025-05-15
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
B-cell Immunity to Influenza (SLVP017) - Years 2 (2010) & 3 (2011)
NCT03020498 ·Status: COMPLETED ·Phase: PHASE4
-
B-cell Immunity to Influenza (SLVP017)- Year 1, 2009
NCT02133781 ·Status: COMPLETED ·Phase: PHASE4
-
Development of Immune Globulin Treatment for Avian Flu
NCT00383071 ·Status: TERMINATED ·Phase: PHASE2
-
Phase I Open-Label Study of Recombinant DNA Plasmid Vaccine, VRC-AVIDNA036-00-VP, Encoding for Influenza Virus H5 Hemagglutinin Protein Given Intradermally
NCT00489931 ·Status: COMPLETED ·Phase: PHASE1
-
Screening for LID Clinical Studies Unit Healthy Volunteer Protocols
NCT01386424 ·Status: RECRUITING
-
Pandemic Influenza Plasmid DNA Vaccines (Needle)
NCT00709800 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of mRNA-1020 and mRNA-1030 Seasonal Influenza Vaccines in Healthy Adults
NCT05333289 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Pilot Study of Influenza Viruses Isolated From Immunocompromised Children and Adolescents
NCT02352389 ·Status: COMPLETED
-
A Study to Assess the Safety and Efficacy of a New Influenza Candidate Vaccine MVA-NP+M1 In Healthy Adults
NCT00993083 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Immunogenicity of Live Influenza A Vaccine for Avian Influenza H7N7
NCT00922259 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluation of Human Immune Responses to Influenza Virus Vaccination in Healthy Volunteers
NCT02385123 ·Status: TERMINATED ·Phase: PHASE4
-
A Study of mRNA-based Influenza and SARS-CoV-2 (COVID-19) Multi-component Vaccines in Healthy Adults
NCT05827926 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Protective Mechanisms Against a Pandemic Respiratory Virus (SLVP024)
NCT03023683 ·Status: COMPLETED ·Phase: PHASE4
-
VRC 309: A Multi-Center, Open-Label, Randomized Phase I Study of an Investigational Influenza DNA Vaccine Followed by 2009/2010 Seasonal Influenza Trivalent Inactivated Vaccine (TIV) Compared to Two Injections of TIV in Adults 45-70 Years
NCT00995982 ·Status: COMPLETED ·Phase: PHASE1
-
Influenza in People With Normal and Weakened Immune Systems
NCT00533182 ·Status: COMPLETED
-
Studying Cell Immune Responses to a Live Flu Vaccine in Healthy Adults
NCT01730144 ·Status: COMPLETED
-
Screening Volunteers for Clinical Trials
NCT01375530 ·Status: RECRUITING
-
Safety, Reactogenicity, and Immunogenicity of Inactivated Influenza A/H7/N7 Vaccine in Healthy Adults
NCT00546585 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
PET-CT Scans in Healthy Volunteers After Flu Vaccination
NCT00769002 ·Status: TERMINATED ·Phase: NA
-
Vaccine Responses to SARS-CoV-2 and Other Emerging Infectious Diseases
NCT05078905 ·Status: RECRUITING
-
The Safety and Immunogenicity Evaluation of Live Attenuated Influenza Vaccine
NCT05284851 ·Status: UNKNOWN ·Phase: PHASE2
-
Comparing the Efficacy and Safety of High-Titer Versus Low-Titer Anti-Influenza Immune Plasma for the Treatment of Severe Influenza A
NCT02572817 ·Status: COMPLETED ·Phase: PHASE3
-
VRC 308: An Open-Label Phase I Study of the Safety and Immunogenicity of an Investigational H1 DNA Influenza Vaccine, VRC-FLUDNA057-00-VP, in Healthy Adults 18-70 Years Old
NCT00973895 ·Status: COMPLETED ·Phase: PHASE1
-
A Study To Learn About The Study Vaccine (Called Self-Amplifying Ribonucleic Acid (RNA)) For The Prevention of Influenza
NCT05227001 ·Status: COMPLETED ·Phase: PHASE1
-
A Phase I Study Priming With an Inactivated A/H7N9 Influenza Virus Vaccine With or Without MF59 Adjuvant Followed by Live Attenuated A/H7N9 Influenza Virus Vaccine
NCT02251288 ·Status: COMPLETED ·Phase: PHASE1