200 Participants NeededMy employer runs this trial

BNT162b2 Vaccine for COVID-19

Recruiting at 4 trial locations
Age: 18 - 65
Sex: Any
Trial Phase: Phase 4
Sponsor: BioNTech SE
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial examines the safety and effects of an updated COVID-19 vaccine, BNT162b2, in adults aged 18 to 64. Participants will receive one injection, either the BNT162b2 vaccine or the Tdap vaccine (which targets tetanus, diphtheria, and whooping cough), with neither participants nor researchers knowing which one until the end. The trial focuses on assessing vaccine safety and measuring levels of the SARS-CoV-2 spike protein (a part of the virus) after vaccination. It is suitable for healthy adults who haven't had a recent COVID-19 infection or vaccination and are not at higher risk for severe COVID-19. Participants will engage in the study for about 12 months. As a Phase 4 trial, this study involves an FDA-approved vaccine and aims to understand its benefits for more patients.

What is the safety track record for these treatments?

Research has shown that the BNT162b2 vaccine is safe. Studies with teenagers and adults indicate that the vaccine is generally well-tolerated, with most individuals experiencing only mild reactions, such as soreness at the injection site. These studies have not identified any serious safety issues.

Real-world data support these findings, though some rare side effects, like Bell's palsy and Guillain–Barré syndrome, have been observed. However, these occurrences are uncommon, and for most individuals, the benefits of the vaccine outweigh the risks.

The vaccine is widely used and approved for preventing COVID-19, further enhancing its safety reputation.12345

Why are researchers enthusiastic about this study treatment?

The BNT162b2 vaccine is unique because it is a variant-adapted vaccine designed specifically to tackle emerging strains of COVID-19. Unlike the standard vaccines that were initially developed for the original strain, this new version aims to provide enhanced protection against new variants, potentially offering better immunity. Researchers are excited about this treatment because it could maintain or even improve the vaccine's effectiveness as the virus evolves, thus providing a critical tool in the ongoing fight against COVID-19.

What evidence suggests that this trial's treatments could be effective for COVID-19?

Research shows that the BNT162b2 vaccine, which participants in this trial may receive, effectively prevents COVID-19. Studies have found it to be 95% effective at stopping the virus and completely preventing hospital visits due to COVID-19. It is over 90% effective at preventing severe cases of the disease. These results, derived from clinical trials and large studies, demonstrate its strong protective benefits. Another group in this trial will receive the Tdap vaccine as an active comparator.16789

Who Is on the Research Team?

PC

Pfizer CT.gov Call Center

Principal Investigator

Pfizer

Are You a Good Fit for This Trial?

This trial is for healthy adults aged 18 to 64 who are medically stable, have not recently had COVID-19 or a recent vaccine, and do not have health conditions that put them at higher risk of severe COVID-19 complications.

Inclusion Criteria

I am healthy, 18 to 64 years old, and not at high risk for severe COVID-19.

Exclusion Criteria

I tested positive for COVID-19 in the past 6 months.
I have recently received or plan to get a COVID-19 vaccine during the study.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive a single injection of either the BNT162b2 vaccine or the Tdap vaccine on Day 1

1 day
1 visit (in-person)

Follow-up

Participants are monitored for safety and SARS-CoV-2 spike protein levels over the course of the study

12 months

What Are the Treatments Tested in This Trial?

Interventions

  • BNT162b2 Vaccine
  • Tdap Vaccine

Trial Overview

The study compares an updated COVID-19 vaccine (BNT162b2) with the Tdap vaccine (for tetanus, diphtheria, and pertussis). Participants are randomly assigned to get one shot of either vaccine without knowing which they receive. The study lasts about a year.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: BNT162b2 VaccineExperimental Treatment1 Intervention
Group II: Tdap VaccineActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

BioNTech SE

Lead Sponsor

Trials
84
Recruited
120,000+

Prof. Dr. Ugur Sahin

BioNTech SE

Chief Executive Officer since 2008

MD from University of Cologne

Prof. Özlem Türeci

BioNTech SE

Chief Medical Officer since 2018

MD from Saarland University

Pfizer

Industry Sponsor

Trials
4,712
Recruited
50,980,000+
Known For
Vaccine Innovations
Top Products
Viagra, Zoloft, Lipitor, Prevnar 13

Albert Bourla

Pfizer

Chief Executive Officer since 2019

PhD in Biotechnology of Reproduction, Aristotle University of Thessaloniki

Patrizia Cavazzoni profile image

Patrizia Cavazzoni

Pfizer

Chief Medical Officer

MD from McGill University

Citations

Safety and Efficacy of the BNT162b2 mRNA Covid-19 ...

BNT162b2 was 95% effective in preventing Covid-19 (95% credible interval, 90.3 to 97.6). , corresponding to 94.6% vaccine efficacy … a vaccine ...

Effectiveness of Pfizer Vaccine BNT162b2 Against SARS-CoV ...

It also highlighted a 100% effectiveness in preventing COVID-19-associated hospitalizations and 83.3% in preventing COVID-19-related deaths from ...

Effectiveness of COVID-19 Pfizer-BioNTech BNT162b2 ...

The efficacy of the BNT162b2 (Pfizer-BioNTech) vaccine against laboratory-confirmed COVID-19 exceeded 90% in clinical trials that included ...

Pfizer and BioNTech Conclude Phase 3 Study of COVID ...

Primary efficacy analysis demonstrates BNT162b2 to be 95% effective against COVID-19 beginning 28 days after the first dose; 170 confirmed ...

Effectiveness of mRNA BNT162b2 COVID-19 vaccine up to ...

BNT162b2 mRNA vaccine (tozinameran, Pfizer–BioNTech) showed 95% or greater efficacy against symptomatic and severe COVID-19 disease due to SARS-CoV-2.1 1.

Safety of COVID-19 Pfizer-BioNtech (BNT162b2) mRNA ...

In clinical trials with teenagers, the BNT162b2 vaccination revealed a very high level of safety and efficacy. For instance, although adolescents who received ...

Real-world safety data for the Pfizer BNT162b2 SARS-CoV-2 ...

The Pfizer BNT162b2 vaccine showed a reassuring safety profile in clinical trials, but real-world data are scarce. Bell's palsy, herpes zoster, Guillain–Barré ...

Pfizer-BioNTech COVID-19 Vaccine | ACIP

Pfizer-BioNTech COVID-19 vaccine reduced symptomatic COVID-19 when compared to placebo (vaccine efficacy: 91.1% (95% CI 88.8–93.1%))

Safety of the fourth COVID-19 BNT162b2 mRNA (second ...

The most frequent adverse event reported was pain at the injection site, and most of the reported adverse events were considered mild.