NEW YORK--(BUSINESS WIRE)--Pfizer Inc. (NYSE:PFE) announced today it will present the results of a Phase 2, randomized study to evaluate co-administration of the company’s investigational meningococcal group B vaccine, bivalent recombinant LP2086 (rLP2086), with a licensed quadrivalent human papillomavirus vaccine (HPV4), at IDWeek 2014™ in Philadelphia. Data demonstrated immune responses to both vaccines were generated after concomitant administration of bivalent rLP2086 and HPV4. Prespecified noninferiority criteria were met for the bivalent rLP2086 antigens studied and three of the four antigens for HPV4.
“We are pleased to present data on our investigational meningococcal group B vaccine at IDWeek 2014,” said Dr. Emilio Emini, senior vice president of Vaccine Research and Development for Pfizer Inc. “We look forward to sharing additional data from the ongoing Phase 2 and Phase 3 clinical studies of our vaccine candidate.”
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