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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

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

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

Getting a Flu Vaccine and a COVID-19 Vaccine at the Same Time | CDC
Getting a Flu Vaccine and a COVID-19 Vaccine at the Same Time | CDC

Looking beyond COVID-19 vaccine phase 3 trials | Nature Medicine
Looking beyond COVID-19 vaccine phase 3 trials | Nature Medicine

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

Homologous and Heterologous Covid-19 Booster Vaccinations | NEJM
Homologous and Heterologous Covid-19 Booster Vaccinations | NEJM

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

Quadrivalent meningococcal tetanus toxoid-conjugate booster vaccination in  adolescents and adults: phase III randomized study | Pediatric Research
Quadrivalent meningococcal tetanus toxoid-conjugate booster vaccination in adolescents and adults: phase III randomized study | Pediatric Research

Monitoring Visits in Clinical Trials
Monitoring Visits in Clinical Trials

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 -

UC Davis and Pfizer partner on two new COVID-19 booster vaccine clinical  trials
UC Davis and Pfizer partner on two new COVID-19 booster vaccine clinical trials

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

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 ...

Effect of a 2-week interruption in methotrexate treatment versus continued  treatment on COVID-19 booster vaccine immunity in adults with inflammatory  conditions (VROOM study): a randomised, open label, superiority trial - The  Lancet
Effect of a 2-week interruption in methotrexate treatment versus continued treatment on COVID-19 booster vaccine immunity in adults with inflammatory conditions (VROOM study): a randomised, open label, superiority trial - The Lancet

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

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)

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

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

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

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

Safety and immunogenicity of seven COVID-19 vaccines as a third dose ( booster) following two doses of ChAdOx1 nCov-19 or BNT162b2 in the UK (COV- BOOST): a blinded, multicentre, randomised, controlled, phase 2 trial -
Safety and immunogenicity of seven COVID-19 vaccines as a third dose ( booster) following two doses of ChAdOx1 nCov-19 or BNT162b2 in the UK (COV- BOOST): a blinded, multicentre, randomised, controlled, phase 2 trial -

Bivalent Omicron BA.1–Adapted BNT162b2 Booster in Adults Older than 55  Years | NEJM
Bivalent Omicron BA.1–Adapted BNT162b2 Booster in Adults Older than 55 Years | NEJM

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

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

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

Participants sought for COVID-19 vaccine trial for booster and variant  protection
Participants sought for COVID-19 vaccine trial for booster and variant protection

Coronavirus (COVID-19) Vaccines | CardioSmart – American College of  Cardiology
Coronavirus (COVID-19) Vaccines | CardioSmart – American College of Cardiology

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