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Antibody persistence and immune memory response following primary  vaccination and boosting with live attenuated SA 14-14-2 Japanese  encephalitis vaccine (CD-JEV) in Bangladesh: A phase 4 open-label clinical  trial - ScienceDirect
Antibody persistence and immune memory response following primary vaccination and boosting with live attenuated SA 14-14-2 Japanese encephalitis vaccine (CD-JEV) in Bangladesh: A phase 4 open-label clinical trial - ScienceDirect

NIH begins clinical trial evaluating second COVID-19 booster shots in  adults | National Institutes of Health (NIH)
NIH begins clinical trial evaluating second COVID-19 booster shots in adults | National Institutes of Health (NIH)

Safety, immunogenicity and antibody persistence of a bivalent  Beta-containing booster vaccine against COVID-19: a phase 2/3 trial |  Nature Medicine
Safety, immunogenicity and antibody persistence of a bivalent Beta-containing booster vaccine against COVID-19: a phase 2/3 trial | Nature Medicine

PRACT: a pragmatic randomized adaptive clinical trial protocol to  investigate a culturally adapted brief negotiational intervention for  alcohol use in the emergency department in Tanzania | Trials | Full Text
PRACT: a pragmatic randomized adaptive clinical trial protocol to investigate a culturally adapted brief negotiational intervention for alcohol use in the emergency department in Tanzania | Trials | Full Text

Safety and immunogenicity of heterologous versus homologous prime-boost  schedules with an adenoviral vectored and mRNA COVID-19 vaccine (Com-COV):  a single-blind, randomised, non-inferiority trial - The Lancet
Safety and immunogenicity of heterologous versus homologous prime-boost schedules with an adenoviral vectored and mRNA COVID-19 vaccine (Com-COV): a single-blind, randomised, non-inferiority trial - The Lancet

Vaccines
Vaccines

COVID vaccinations: questions and answers about the rollout in North  Yorkshire - NHS North Yorkshire CCG
COVID vaccinations: questions and answers about the rollout in North Yorkshire - NHS North Yorkshire CCG

How To Improve Patient Recruitment In Clinical Trials? | Credevo Articles
How To Improve Patient Recruitment In Clinical Trials? | Credevo Articles

Cohort Profile:The Danish National Cohort Study of Effectiveness and Safety  of SARS-CoV-2 vaccines (ENFORCE) | BMJ Open
Cohort Profile:The Danish National Cohort Study of Effectiveness and Safety of SARS-CoV-2 vaccines (ENFORCE) | BMJ Open

Virology Research Clinic - University of Washington
Virology Research Clinic - University of Washington

Evaluation of BNT162b2 Covid-19 Vaccine in Children Younger than 5 Years of  Age | NEJM
Evaluation of BNT162b2 Covid-19 Vaccine in Children Younger than 5 Years of Age | NEJM

Ongoing booster vaccine trial seeks vaccinated volunteers | Newsroom
Ongoing booster vaccine trial seeks vaccinated volunteers | Newsroom

Safety and immunogenicity of a bivalent SARS-CoV-2 protein booster vaccine,  SCTV01C, in adults previously vaccinated with mRNA vaccine: a randomized,  double-blind, placebo-controlled phase 1/2 clinical trial - eBioMedicine
Safety and immunogenicity of a bivalent SARS-CoV-2 protein booster vaccine, SCTV01C, in adults previously vaccinated with mRNA vaccine: a randomized, double-blind, placebo-controlled phase 1/2 clinical trial - eBioMedicine

Home | COV-Boost
Home | COV-Boost

Immunogenicity and safety of NVSI-06-07 as a heterologous booster after  priming with BBIBP-CorV: a phase 2 trial | Signal Transduction and Targeted  Therapy
Immunogenicity and safety of NVSI-06-07 as a heterologous booster after priming with BBIBP-CorV: a phase 2 trial | Signal Transduction and Targeted Therapy

Department of Health and Social Care on Twitter: "Everyone aged 16 and over  is eligible for the #COVID19 booster from three months after their second  dose. Book an appointment online or find
Department of Health and Social Care on Twitter: "Everyone aged 16 and over is eligible for the #COVID19 booster from three months after their second dose. Book an appointment online or find

Pfizer seeks authorization for new Covid booster, without fresh clinical  data
Pfizer seeks authorization for new Covid booster, without fresh clinical data

Immunogenicity and reactogenicity of BNT162b2 booster in ChAdOx1-S-primed  participants (CombiVacS): a multicentre, open-label, randomised,  controlled, phase 2 trial - The Lancet
Immunogenicity and reactogenicity of BNT162b2 booster in ChAdOx1-S-primed participants (CombiVacS): a multicentre, open-label, randomised, controlled, phase 2 trial - The Lancet

Frontiers | Review of Clinical Trials of COVID-19 Vaccination Booster in  SARS-CoV-2 Variants Era: To Take It or Not To Take It
Frontiers | Review of Clinical Trials of COVID-19 Vaccination Booster in SARS-CoV-2 Variants Era: To Take It or Not To Take It

UK volunteers to receive Moderna Omicron COVID-19 booster vaccine in  clinical study | NIHR
UK volunteers to receive Moderna Omicron COVID-19 booster vaccine in clinical study | NIHR

RNAimmune receives FDA approval for trial of Covid-19 booster
RNAimmune receives FDA approval for trial of Covid-19 booster

Protocol for a multicentre randomised controlled trial examining the  effects of temporarily pausing Bruton tyrosine kinase inhibitor therapy to  coincide with SARS-CoV-2 vaccination and its impact on immune responses in  patients with
Protocol for a multicentre randomised controlled trial examining the effects of temporarily pausing Bruton tyrosine kinase inhibitor therapy to coincide with SARS-CoV-2 vaccination and its impact on immune responses in patients with

Immunobridging trials: Bringing medicines to patients faster
Immunobridging trials: Bringing medicines to patients faster

Effects of temporarily suspending low-dose methotrexate treatment for 2  weeks after SARS-CoV-2 vaccine booster on vaccine response in  immunosuppressed adults with inflammatory conditions: protocol for a  multicentre randomised controlled trial and ...
Effects of temporarily suspending low-dose methotrexate treatment for 2 weeks after SARS-CoV-2 vaccine booster on vaccine response in immunosuppressed adults with inflammatory conditions: protocol for a multicentre randomised controlled trial and ...

COVID-19 Boosters: Why You Should Schedule One Now
COVID-19 Boosters: Why You Should Schedule One Now

Efficacy and immunogenicity of R21/Matrix-M vaccine against clinical  malaria after 2 years' follow-up in children in Burkina Faso: a phase 1/2b  randomised controlled trial - The Lancet Infectious Diseases
Efficacy and immunogenicity of R21/Matrix-M vaccine against clinical malaria after 2 years' follow-up in children in Burkina Faso: a phase 1/2b randomised controlled trial - The Lancet Infectious Diseases

Pneumococcal conjugate vaccine 13 delivered as one primary and one booster  dose (1 + 1) compared with two primary doses and a booster (2 + 1) in UK  infants: a multicentre, parallel
Pneumococcal conjugate vaccine 13 delivered as one primary and one booster dose (1 + 1) compared with two primary doses and a booster (2 + 1) in UK infants: a multicentre, parallel

Adopting a New Agile Approach to CRO Clinical Trial Management - Clinical  Trial Services, UK | PHARMExcel
Adopting a New Agile Approach to CRO Clinical Trial Management - Clinical Trial Services, UK | PHARMExcel

NIH clinical trial evaluating Moderna COVID-19 variant vaccine begins |  National Institutes of Health (NIH)
NIH clinical trial evaluating Moderna COVID-19 variant vaccine begins | National Institutes of Health (NIH)