Viral Specific T-cells for Treatment of COVID-19
NCT04406064 · Status: WITHDRAWN · Phase: PHASE2 · Type: INTERVENTIONAL
Last updated 2021-01-19
Summary
The purpose of this research study is to learn more about the use of viral specific T-lymphocytes (VSTs) when given in the presence of COVID-19 signs and symptoms, caused by the virus SARS-CoV-2. VSTs are cells specially designed to fight viral infections. These cells are created from a blood sample collected from a donor who has recovered from COVID-19 infection. VSTs are investigational meaning that they are not approved by the Food and Drug Administration (FDA).
COVID-19 is a new virus and treatment options are evolving rapidly. VSTs have been successfully used to treat many different viral infections and may be beneficial in treating COVID-19 in the absence of other treatments.
Conditions
Interventions
- BIOLOGICAL
-
Viral Specific T-cells (VSTs)
VSTs will be infused into study participants who have evidence of SARS-CoV-2 infection.
Sponsors & Collaborators
-
Hoxworth Blood Center
collaborator OTHER -
Children's Hospital Medical Center, Cincinnati
lead OTHER
Principal Investigators
-
Adam Nelson, MBBS, FRACP · Children's Hospital Medical Center, Cincinnati
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 1 Day
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-01-31
- Primary Completion
- 2024-06-30
- Completion
- 2025-06-30
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Stem Cell Educator Therapy Treat the Viral Inflammation in COVID-19
NCT04299152 ·Status: UNKNOWN ·Phase: PHASE2
-
Study of RV521 in the Treatment of Adult Subjects Who Have Undergone HCT With an URTI With RSV
NCT04267822 ·Status: WITHDRAWN ·Phase: PHASE2
-
R-MVST Cells for Treatment of Viral Infections in Children and Young Adults
NCT06926894 ·Status: RECRUITING ·Phase: PHASE1
-
Human COVID-19 Immunoglobulin (COVID-HIG) Therapy for COVID-19 Patients
NCT05173441 ·Status: UNKNOWN ·Phase: PHASE2
-
Study of TB006 in Outpatient Patients With Mild to Moderate COVID-19
NCT04801056 ·Status: WITHDRAWN ·Phase: PHASE1
-
R-MVST Cells for Treatment of Viral Infections
NCT05183490 ·Status: RECRUITING ·Phase: PHASE1
-
A Study of the Safety and Efficacy of A-60444 in Adults With Respiratory Syncytial Virus (RSV) Infection Following HSCT
NCT00232635 ·Status: COMPLETED ·Phase: PHASE2
-
Trial to Evaluate the Safety, Tolerability, and Pharmacokinetics of MEDI-524 in Healthy Adults
NCT00192465 ·Status: COMPLETED ·Phase: PHASE1
-
Study Evaluating IGSC 20% Flexible Dosing in Treatment-Experienced and Treatment-Naive Subjects With Primary Immunodeficiency
NCT03814798 ·Status: WITHDRAWN ·Phase: PHASE3
-
Delayed Heterologous SARS-CoV-2 Vaccine Dosing (Boost) After Receipt of EUA Vaccines
NCT04889209 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Safety of and Immune Response to Recombinant Live-Attenuated Parainfluenza Type 1 Virus Vaccine
NCT00641017 ·Status: COMPLETED ·Phase: PHASE1
-
Outpatient Treatment With Anti-Coronavirus Immunoglobulin
NCT04910269 ·Status: RECRUITING ·Phase: PHASE3
-
PROSPECTIVE OPEN LABEL CLINICAL TRIAL TO ADMINISTER A BOOSTER DOSE OF PFIZER/BIONTECH OR MODERNA COVID-19 VACCINE IN HIGH-RISK INDIVIDUALS
NCT05279365 ·Status: UNKNOWN ·Phase: PHASE2/PHASE3
-
Study of VYD2311 for the Prevention of COVID-19
NCT07298434 ·Status: RECRUITING ·Phase: PHASE3
-
Remdesivir for the Treatment of Upper Respiratory Tract Infection Due to RSV in Immunocompromised Individuals
NCT06817889 ·Status: RECRUITING ·Phase: PHASE2
-
PUL-042 Treatment in Patients With Parainfluenza Virus (PIV), Human Metapneumovirus (hMPV) or Respiratory Syncytial Virus (RSV)
NCT06665100 ·Status: RECRUITING ·Phase: PHASE2
-
A Study to Assess the Safety and Immunogenicity of a COVID-19 Vaccine Booster in Healthy Adults
NCT05389319 ·Status: RECRUITING ·Phase: PHASE1
-
Study of the Infectivity, Safety and Immunogenicity of Two Recombinant, Live-Attenuated, B/HPIV3 Vectored Vaccines Expressing the Fusion Glycoprotein of HMPV Delivered by Nasal Spray to HPIV3-Seropositive Children 24 to <60 Months of Age
NCT06546423 ·Status: COMPLETED ·Phase: PHASE1
-
Evaluating the Safety and Immune Response to Two Admixtures of a Tetravalent Dengue Virus Vaccine
NCT01436422 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of the Investigational Monoclonal Antibody, VYD2311, in Healthy Participants
NCT06523153 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1
-
Safety, Tolerability, and Efficacy of Anti-Spike (S) SARS-CoV-2 Monoclonal Antibodies for the Treatment of Ambulatory Adult and Pediatric Patients With COVID-19
NCT04425629 ·Status: TERMINATED ·Phase: PHASE3
-
A Randomized, Open-label, Dose-ranging Study in Adults and Pediatric Individuals ≥ 12 Years of Age to Assess the Safety, Immunogenicity, Pharmacokinetics, and Pharmacodynamics of AZD7442, for Pre-exposure Prophylaxis of COVID-19
NCT05375760 ·Status: TERMINATED ·Phase: PHASE2
-
A Study of Immune Responses to the Virus That Causes COVID-19
NCT04431414 ·Status: COMPLETED
-
Presatovir in Hematopoietic Cell Transplant Recipients With Respiratory Syncytial Virus Infection of the Upper Respiratory Tract
NCT02254408 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Preliminary Immunogenicity Study of Inactivated Vaccine for Prevention of Rotavirus Infection
NCT04626856 ·Status: UNKNOWN ·Phase: PHASE1