Biological E. Limited (BE), a Hyderabad-based Vaccine and Pharmaceutical Company, announced the publication of Phase-III clinical trials results of BE’s 14-Valent Pneumococcal Conjugate Vaccine (PCV) (PNEUBEVAX 14TM; BE-PCV-14) conducted in paediatric population (6-8-week age group). The study results have been accepted and published by Vaccine, a reputed peer-reviewed international journal.
In this study, the immunogenicity and safety of the BE’s 14-Valent PCV containing two additional epidemiologically important serotypes (22F and 33F) were evaluated in infants, in comparison to the licensed comparator vaccine PCV-13.
This was a pivotal Phase-III single blind randomized active-controlled study conducted at 12 sites across India in 1290 healthy infants at 6-10-14 weeks dosing schedule to assess immunogenic non-inferiority and safety of PNEUBEVAX 14TM. Immunogenicity was assessed by measuring anti-Pneumococcal Capsular Polysaccharide (anti-PnCPS) IgG concentration and functional antibody titres through Opsonophagocytic Activity (OPA), one month after completing a three-dose schedule. Cross- protection against serotype 6A offered by serotype 6B was also assessed in this study.
PNEUBEVAX 14TM was found to be safe and induced robust and functional serotype specific immune responses to all 14 serotypes. It also elicited cross-protective immune response against serotype 6A.These findings suggest that PNEUBEVAX 14TM can be safely administered to infants and achieve protection against pneumococcal disease caused by serotypes covered in the vaccine.
Ms. Mahima Datla, Managing Director, Biological E. Limited, said: “we are pleased to announce that results have been published by the Vaccine Journal. We have reached a significant milestone in our ongoing fight against pneumococcal disease, and we are now one step closer to the finish line with our 14-Valent PCV Vaccine PNEUBEVAX 14TM. These findings underscore the success of our R&D and serve as a source of motivation for all of us at BE.’’
