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Condition / disease
Location
Status: Recruiting

A Phase 3 Study to Evaluate the Immunogenicity and Safety of Minhai's PCV13-DT/TT Vaccine As Compared to Pfizer's PCV13 Vaccine

The goal of this clinical trial is to evaluate the immunogenicity and safety of Minhai's 13-valent Pneumococcal Polysaccharide Conjugate Vaccine (PCV13-DT/TT) as compared to Pfizer's 13-valent Pneumococcal Conjugate Vaccine (PCV13) when co-administered with Hexavalent Vaccines at 2,4, and 12-15 months of age, to healthy infants in Indonesia. This study aims to demonstrate the non-inferiority of the serotype-specific immune responses elicited by the novel PCV13-DT/TT (Pneuminvac) as compared to PCV13(Prevenar 13) one month after the booster dose, and evaluate the safety of PCV13 co-administrated with Hexavalent Vaccine(Hexaxim).

Participants needed: 500
Trial details
Phase: Phase 3Age: 6-8Biological sex: AllType: InterventionalSponsor: Beijing Minhai Biotechnology Co., LtdUpdated: Mar 24, 2025Locations: 3
Eligibility criteria

Healthy infants based on medical history and clinical assessment. [+7]

Use of any investigational product other than that used in the study prior to ra... [+17]