Explore Vaccination Progress by U.S. State
With dozens of COVID-19 vaccines now in clinical trials, it is important to understand the accelerated timelines for development, the different types of vaccines available, and the facts related to vaccine safety and efficacy. Additionally, as vaccines are approved, we will track data on vaccination efforts.
Explore how U.S. states delivered their supplies of COVID-19 vaccines to their residents at vastly different speeds that led to vastly different results.
An interactive tool from our vaccine experts that explores how a vaccine is developed and the differences between a typical timeline and an accelerated timeline.
VIEW-hub is a publicly available interactive tool that displays up-to-date information on vaccine characteristics, and vaccine introduction and use globally. Vaccines include COVID-19 as well as many childhood vaccines in routine immunization programs.
COMIT, the COVID-19 Maternal Immunization Tracker, provides a global picture of national public health policies that influence access to COVID-19 vaccines for pregnant and lactating people.
The Johns Hopkins International Vaccine Access Center provides free, online training to equip people with knowledge to debunk false claims about vaccinations.
Emergency use authorization for Pfizer/BioNTech’s vaccine for U.S. children is unlikely to lead to widespread vaccinations among the nation’s 28 million 5-to-11-year-olds.
Nearly 60% of the U.S. population is fully vaccinated. All of Africa: just 6%. Yet the United States is expanding boosters and authorizing vaccines for children age 5 to 11 years old – and hoarding and wasting additional doses.
This series of brief reports will shed light on COVID-19 vaccine development, allocation and deployment in the United States and globally. Topics will include ensuring the safety and efficacy of Covid-19 vaccines, principles for vaccine allocation, strategies for deployment and delivery of Covid-19 vaccines, vaccine confidence and demand, and the economics of Covid-19 vaccines.
COVID-19 VACCINE MATTERS: A blog series discussing the evolving science and policy of COVID-19 vaccines, led by internationally renowned experts in vaccine development, Dr. Larry Corey of the Univeristy of Washington, and Dr. Chris Beyrer of Johns Hopkins University.
Johns Hopkins University and the University of Washington hosted a high-level symposium, “The Scientific Integrity of COVID-19 Vaccine Efficacy Trials: From Clinical Trials to Public Allocation,” that explored complex issues, brought together leading voices in the field, and put forward a concise plan for protecting the scientific integrity of these ongoing efforts.
American children ages 6 months through 4 years recently became eligible to receive coronavirus vaccinations, after federal regulators and health officials cleared vaccines from Moderna and Pfizer-BioNTech for very young children.
U.S. health authorities are facing a critical decision: whether to offer new COVID-19 booster shots this fall that are modified to better match recent changes of the shape-shifting coronavirus.
When the Food and Drug Administration (FDA) meets at the end of June to discuss whether the vaccine should be modified before the likely rollout of more booster shots in the fall, it will have to make decisions without knowing how the virus will continue to change.
Three doses of Pfizer’s COVID-19 vaccine offer strong protection for children younger than 5, the company announced Monday, another step toward shots for the littlest kids possibly beginning in early summer.
Since the Omicron wave crested in January, multiple studies and datasets have demonstrated that the mRNA vaccines are not nearly as effective against this variant as they were against earlier variants or the original virus.
According to the CDC, Pfizer-BioNTech or Moderna COVID-19 vaccine boosters are preferred for individuals who received the single-dose Johnson & Johnson shot.
Adults 50 and older can now roll up their sleeves for a second COVID-19 booster, as can younger individuals with certain immune-compromising conditions.
More than 16 million Americans rolled up their sleeves last year to get Johnson & Johnson's COVID-19 vaccine because it promised to be a "one and done" shot, but newer information and booster authorizations suggest they should consider a third dose.
The Centers for Disease Control and Prevention (CDC) agreed with the FDA and has updated its vaccine recommendations to include a second booster.
On Tuesday, the FDA announced that it has expanded the emergency use authorization for the two vaccines to allow adults 50 and older to get a second booster as early as fourth months after their first booster dose.
The Food and Drug Administration on Tuesday authorized an extra dose of the Pfizer or Moderna vaccine for Americans 50 and older and for certain younger people with severely weakened immune systems.