100 Participants Needed

RNA-Based Vaccine for COVID-19

Recruiting at 5 trial locations
Age: 18+
Sex: Any
Trial Phase: Phase 3
Sponsor: BioNTech SE
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Pivotal Trial (Near Approval)This treatment is in the last trial phase before FDA approval
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 tests a new version of a COVID-19 vaccine to evaluate its safety and effectiveness against a current virus variant. Participants will receive one shot of the BNT162b2 (Omi LP.8.1) vaccine, which targets a specific COVID-19 strain expected for the 2025-2026 season. The trial is open to individuals 65 and older, as well as adults aged 18 to 64 at higher risk for severe COVID-19, such as those with asthma or diabetes. Participants must have received a COVID-19 vaccine that included Omicron KP.2 more than six months ago. As a Phase 3 trial, this study represents the final step before FDA approval, offering participants the opportunity to contribute to a potentially groundbreaking vaccine.

Will I have to stop taking my current medications?

The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the study contact or your doctor.

Is there any evidence suggesting that this treatment is likely to be safe for humans?

Research has shown that the BNT162b2 vaccine, targeting the LP.8.1 variant of COVID-19, is generally safe. Most side effects are mild to moderate, such as temporary arm pain or tiredness, while serious side effects remain rare. The FDA approved this version of the vaccine, indicating a strong safety record. Designed to match current virus strains, it may enhance the immune response, offering hope for better protection and safety.12345

Why do researchers think this study treatment might be promising?

Unlike the standard COVID-19 vaccines, which often target the original virus strain, BNT162b2 (Omi LP.8.1) specifically targets the Omicron variant. This RNA-based vaccine is unique because it uses a modified version of the mRNA technology that allows it to adapt quickly to new virus mutations, potentially offering broader protection against evolving strains. Researchers are excited about this treatment because it could enhance immunity for higher-risk groups, such as those aged 18–64 with underlying conditions and individuals 65 and older, providing them with more robust defense against severe COVID-19 outcomes.

What evidence suggests that this RNA-based vaccine is effective for COVID-19?

Research shows that the BNT162b2 (Omi LP.8.1) vaccine, administered to participants in this trial, generates a strong immune response against COVID-19. Studies have found that this vaccine, updated for the 2025-2026 season, effectively targets both current and new variants. Tests conducted in labs before human trials demonstrated its superiority over earlier versions. Data also indicate that similar mRNA vaccines have successfully prevented severe COVID-19 cases. This vaccine builds on the success of previously approved versions and shows promise in reducing severe cases.56789

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 adults aged 18-64 at high risk of severe COVID-19 and those over 65. Participants will receive a shot of the BNT162b2 (Omi LP.8.1) vaccine, designed for the variant expected in the 2025-2026 season.

Inclusion Criteria

I am 18 years old or older.
I received an Omicron KP.2 COVID-19 vaccine over 6 months ago and haven't had any other COVID-19 vaccines or the disease since.
I am 18-64 with a condition like asthma, diabetes, heart issues, HIV, depression, Parkinson's, obesity (BMI ≥30), or I smoke.

Exclusion Criteria

History of severe adverse reaction associated with a vaccine and/or severe allergic reaction (eg, anaphylaxis) to any component of the study intervention(s)
I have had myocarditis or pericarditis in the past.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive 1 shot of the BNT162b2 (Omi LP.8.1) 30 µg RNA-based vaccine

1 day
1 visit (in-person)

Follow-up

Participants are monitored for safety, tolerability, and immunogenicity after receiving the vaccine

6 months
At least 3 additional visits (in-person)

What Are the Treatments Tested in This Trial?

Interventions

  • BNT162b2 (Omi LP.8.1)
Trial Overview The study tests safety, tolerability, and immune response to an RNA-based COVID-19 vaccine targeting a new variant. Participants get one dose and are monitored over six months with at least four visits to the clinic.
How Is the Trial Designed?
2Treatment groups
Experimental Treatment
Group I: Group 2: 65 years of age and olderExperimental Treatment1 Intervention
Group II: Group 1: 18 through 64 years of age (higher-risk individuals)Experimental Treatment1 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

Pfizer and BioNTech Announce Topline Data ...Pfizer and BioNTech Announce Topline Data Demonstrating Robust Immune Response With Their LP.8.1-Adapted COVID-19 Vaccine 2025-2026 Formula.
Pfizer/BioNTech- 2025-2026 COVIDEarly Effectiveness of the BNT162b2 KP.2 Vaccine against ... • LP.8.1 vaccine confers improved immune response, in preclinical models,.
NCT07069309 | A Study to Learn About COVID-19 RNA ...All participants in this study will receive 1 shot to their arm of a BNT162b2 (Omi LP. 8.1) 30 µg RNA-based vaccine which targets a circulating variant of SARS ...
Pfizer and BioNTech Receive Positive CHMP Opinion for LP ...Data indicate that the LP.8.1-adapted COVID-19 vaccine confers improved immune response against currently dominant and emerging sublineages ...
Real-World Data Highlight Effectiveness of XBB.1.5- ...Both BNT16b2 and mRNA-1273 XBB.1.5-adapted mRNA vaccines were effective against severe COVID-19 outcomes and conferred similar protection.
SAFETY DATA SHEETPfizer-BioNTech Covid-19 vaccine Tris-Sucrose Omicron LP.8.1 Variant ... Containing PF-08152264 (BNT162b2);COVID-19 Vaccine Containing PF-08152264.
NCT07222384 | A Study to Learn About BNT162b2 (LP.8.1 ...The purpose of this study is to learn about the safety, tolerability, and immunogenicity of an updated vaccine against COVID-19, called BNT162b2 ...
Pfizer and BioNTech's COMIRNATY® Receives U.S. FDA ...The 2025-2026 COVID-19 vaccine formulation targets the SARS-CoV-2 sublineage LP.8.1, in line with FDA guidance to more closely match ...
Clinical Review Memo, August 27, 2025 - COMIRNATY2026 Formula), preferentially using the LP.8.1 strain (COVID-19 Vaccines (2025-2026 Formula) ... The safety data from this study suggest that the ...
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