fbpx

Pfizer-BioNTech’s COVID-19 Influenza Combination Vaccine Demonstrates Mixed Phase 3 Results


Pfizer and BioNTech are evaluating ways to improve upon the influenza B response.

Today, Pfizer announced results from its phase 3 clinical trial for its investigational COVID-19 influenza combination vaccine it has partnered on with BioNTech, as well as results from a separate phase 2 influenza vaccine trial.

The phase 3 combination vaccine study measured 2 primary immunogenicity objectives (immunogenicity against SARS-CoV-2 as well as immunogenicity against influenza A and B), of which 1 was met. Compared to a licensed influenza vaccine, the Pfizer tIRV formulation was noteworthy for eliciting robust influenza A responses, including a continued trend of higher influenza A responses vs a licensed influenza vaccine, while it showed lower geometric mean titers and seroconversion against the influenza B strain.

“We are encouraged by the robust immunogenicity we saw with our combination vaccine against influenza A, which was similar to what we had seen for our initial quadrivalent influenza vaccine where we saw superior relative vaccine efficacy against a comparator flu vaccine,” Annaliesa Anderson, PhD, senior vice president and head, Vaccine Research and Development at Pfizer, said in a statement.

Phase 3 Study Parameters and Takeaways

This was a randomized, observer-blinded study that included over 8000 adults between the ages of 18 through 64 years old. Investigators evaluated the safety, tolerability, and immunogenicity of a single dose combination vaccine candidate against influenza and COVID-19.

The vaccine candidate was compared to a licensed influenza vaccine and the companies’ licensed COVID-19 vaccine given at the same visit. The primary immunogenicity objectives were to demonstrate that the antibody responses to influenza and to SARS-CoV-2 elicited by the combination vaccine candidate were non-inferior to the standard of care.

In addition, to the aforementioned results against influenza, the formulation demonstrated comparable responses against SARS-CoV-2 vs the companies’ licensed COVID-19 vaccine.

No safety signals with the combination vaccine have been identified in an ongoing safety data review. Participants who received a licensed influenza and COVID-19 vaccine with coadministration continued to elicit robust immune responses against both influenza and COVID-19 with no safety signals identified to date.

What You Need to Know

The combination vaccine demonstrated strong immunogenicity against influenza A, similar to Pfizer’s previous quadrivalent influenza vaccine.

While the vaccine performed well against influenza A, it elicited lower geometric mean titers and seroconversion against the influenza B strain.

The combination vaccine’s immunogenicity against SARS-CoV-2 was comparable to the licensed COVID-19 vaccine, with no significant safety concerns identified in the ongoing review.

Pfizer Influenza Vaccine Phase 2 Study

In a separate phase 2 trial, Pfizer evaluated its trivalent influenza mRNA standalone vaccine candidate which demonstrated robust immunogenicity in individuals 18-64 years of age. They enrolled 450 participants who were randomized to receive investigational mRNA-based influenza vaccines or influenza vaccines approved by the FDA.

Next Steps

After the reporting of the top-line data results the companies are evaluating adjustments to improve immune responses against influenza B the investigational vaccine and will discuss next steps with health authorities weighing their next move.

“We are committed to developing vaccines that will reduce the burden of respiratory diseases and believe that combination vaccines are the most efficient way to do this. Today’s results provide insight and direction towards achieving this goal, and we remain optimistic about our combination COVID-19 and influenza program, for which we are evaluating the next steps,” said Pfizer’s Anderson, PhD.

Reference
1.Pfizer and BioNTech Provide Update on mRNA-based Combination Vaccine Program Against Influenza and COVID-19 in Individuals 18-64 Years of Age. Pfizer news statement. August 16, 2024. Accessed August 16, 2024.
https://www.pfizer.com/news/press-release/press-release-detail/pfizer-and-biontech-provide-update-mrna-based-combination



Source link

Daily Dose of Insights

Get a daily infusion of knowledge with our latest blog updates.

We don’t spam! Read our privacy policy for more info.

LEAVE A REPLY

Please enter your comment!
Please enter your name here

Natural Hair Growth Oil

Related articles

Natural Hair Growth Oil

I’ve written quite a few natural hair care articles over the years. Recipes like nourishing conditioner and...

Long-Acting Lipoglycopeptides for the Treatment of Severe Infections

Long-acting lipoglycopeptides (LGPs) including dalbavancin, oritavancin, and telavancin were developed with their unique pharmacokinetic property of prolonged...

Fried Calamari | The Recipe Critic

This website may contain affiliate links and advertising so that we can provide recipes to you. Read...

Nirmatrelvir/Ritonavir and Molnupiravir Against New Variants

Evolving efficacy of nirmatrelvir/ritonavir and molnupiravir against new COVID-19 variants.Image credits: UnsplashThree therapies have received either full...