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NCT06817187

Clinical Study on the Combined Administration of 15-Valent Pneumococcal Conjugate Vaccine and Diphtheria, Tetanus, Pertussis Vaccine

Completed Phase 3 Last updated 10 February 2025
What this trial tests

Phase 3 trial testing 15-Valent Pneumococcal Conjugate Vaccine and Diphtheria, Tetanus and Acellular pertussis (Component) Combined Vaccine (Adsorbed) in Streptococcus Pneumoniae Infections in 1,110 participants. Completed in 13 March 2024.

Timeline
16 September 2021
Primary endpoint
13 March 2024
13 March 2024

Quick facts

Lead sponsorBeijing Zhifei Lvzhu Biopharmaceutical Co., Ltd
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsequential
Maskingnone
Primary purposeprevention
Enrollment1,110
Start date16 September 2021
Primary completion13 March 2024
Estimated completion13 March 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Beijing Zhifei Lvzhu Biopharmaceutical Co., Ltd — full company profile →

Who can join

Adults 3 Months to 3 Months, any sex, with Streptococcus Pneumoniae Infections. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This clinical study aims to evaluate the mutual influence of combined administration of 15-Valent Pneumococcal Conjugate Vaccine and Diphtheria, Tetanus, Pertussis Vaccine in the target population

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Trials by the same sponsor.

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