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Phase 3 Safety and Efficacy of AZD1222 (ChAdOx1 nCoV-19) Covid-19 Vaccine |  NEJM
Phase 3 Safety and Efficacy of AZD1222 (ChAdOx1 nCoV-19) Covid-19 Vaccine | NEJM

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)

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

A Bivalent Omicron-Containing Booster Vaccine against Covid-19 | NEJM
A Bivalent Omicron-Containing Booster Vaccine against Covid-19 | NEJM

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

GCT to Perform Booster Visits in Russia
GCT to Perform Booster Visits in Russia

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

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

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 ...

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

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

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

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

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

Vaccines
Vaccines

Immunogenicity of a single-dose compared with a two-dose primary series  followed by a booster dose of ten-valent or 13-valent pneumococcal  conjugate vaccine in South African children: an open-label, randomised,  non-inferiority trial -
Immunogenicity of a single-dose compared with a two-dose primary series followed by a booster dose of ten-valent or 13-valent pneumococcal conjugate vaccine in South African children: an open-label, randomised, non-inferiority trial -

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

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

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

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

Volunteers needed for COVID-19 booster trial | KPWHRI
Volunteers needed for COVID-19 booster trial | KPWHRI

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

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

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