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Viernes 2 oct 2026SEC · NASDAQ biomédico

Calendario›SNY›PCV21 vaccine

PCV21 vaccine

Study of a 21-valent Pneumococcal Conjugate Vaccine in Healthy Infants From Approximately 2 Months of Age

Ensayo de Sanofi en Inmunización neumocócica · Voluntarios sanos.

Fase
Fase 3
Estado
En marcha, sin reclutar
Participantes
1.092
previstos
Centros
49
Fin del objetivo primario
ago 2027
estimado por el promotor

Qué significa cada fase y cada estado.

Estudio de intervención, aleatorizado, cuádruple ciego. Comenzó en may 2025.

Qué mide

Tasa de serorespuesta para serotipos PCV21 y 15vPCV (30 days post-toddler dose) (del registro, en inglés)

Qué se prueba

Se mide si la vacuna PCV21 es segura y estimula la generación de anticuerpos comparada con la vacuna 15vPCV cuando se administran junto a las vacunas pediátricas de rutina en lactantes de aproximadamente 2 meses.

Lo que dice el documentomeasure whether PCV21 vaccine (investigational pneumococcal conjugate vaccine) is safe and can help the body to develop germ-fighting agents called "antibodies" (immunogenicity) compared with 15vPCV (Vaxneuvance, licensed pneumococcal conjugate vaccine) when they are administered with routine pediatric vaccines in infants aged from approximately 2 months (42 to 112 days).

Traducción automática (claude-haiku-4-5-20251001). Lo comprobado es la cita: está literal en el documento y sus cifras cuadran con las de la frase. Todavía no la ha leído una persona.

Cómo lo describe el promotor

En el documentoEn inglés, del registroThis study is a Phase 3, randomized, modified double-blind study which aims to measure whether PCV21 vaccine (investigational pneumococcal conjugate vaccine) is safe and can help the body to develop germ-fighting agents called "antibodies" (immunogenicity) compared with 15vPCV (Vaxneuvance, licensed pneumococcal conjugate vaccine) when they are administered with routine pediatric vaccines in infants aged from approximately 2 months (42 to 112 days). The study duration per participant will be up to approximately 20 months. The study vaccines (either PCV21 or 15-valent pneumococcal vaccines) will be administered at approximately 2, 4, and 11 to 15 months of age or at approximately 2, 3, 4, and 11 to 15 months of age (for preterm infants). Routine pediatric vaccines will be given at the same timepoints, as per local practice / recommendations. • There will be 5 (for full-term infants) or 6 (for preterm infants) study visits: * Full-term infants: Visit (V)01, V02 separated from V01 by 60 days, V03 separated from V02 by 30 days, V04 at 11 months of age until 15 months of age, V05 separated from V04 by 30 days. * Preterm infants: Visit (V)01, V02 separated from V01 by 30 days, V03 separated from V02 by 30 days, V04 separated from V03 by 30 days, V05 at 11 months of age until 15 months of age, V06 separated from V05 by 30 days.

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Todos los de SNY, en su ficha.

Ficha completa en ClinicalTrials.gov (NCT06975878), actualizada en feb 2026.