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PivotalWire
Viernes 2 oct 2026SEC · NASDAQ biomédico

Calendario›BNTX›BNT162b2

BNT162b2

A Study of COVID-19 Vaccine(s) in Children and Adults

Ensayo de BioNTech SE en Vacunas contra la COVID-19.

Fase
Fase 3
Estado
Reclutando pacientes
Participantes
700
previstos
Centros
14
Fin del objetivo primario
abr 2027
estimado por el promotor

Qué significa cada fase y cada estado.

Estudio de intervención, aleatorizado, triple ciego. Comenzó en ago 2026.

Lo que ha cambiado

Movimientos registrados desde que PivotalWire vigila este ensayo. Un retraso no se anuncia: se ve comparando, y esto es la comparación ya hecha.

VistoQué se mueveCambio
29 sep 2026EstadoAún sin reclutar → Reclutando pacientes
29 sep 2026Lectura de resultadosabr 2027 → abr 2027

Qué mide

Porcentaje de participantes que reportan reacciones locales o eventos sistemicos (For up to 7 days after vaccination) (del registro, en inglés)

Qué se prueba

Se prueban vacunas actualizadas contra la COVID-19 (BNT162b2) en participantes de 5 a 64 anos con factores de riesgo y en mayores de 65 anos.

Lo que dice el documentothe safety and effects of updated COVID-19 vaccines (called BNT162b2) in participants 5 Through 64 Years of Age with risk factors for Severe COVID-19, and Participants 65 Years of Age and Older.

Traducción automática (claude-sonnet-5). 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 registroThe purpose of this study is to learn about the safety and effects of updated COVID-19 vaccines (called BNT162b2) in participants 5 Through 64 Years of Age with risk factors for Severe COVID-19, and Participants 65 Years of Age and Older. This study is seeking participants who: * are medically stable * have not had a recent COVID-19 infection or a recent COVID-19 vaccination * have not received certain routine vaccines recently * participants that are 5 through 64 years of age will need to have at least 1 medical condition that increase their risk of complications from COVID-19. Participants in Cohort 1 of this study will receive a single age-appropriate dose (30 mcg for participants aged ≥12 years; 10 mcg for participants aged 5-11 years) of BNT162b2 vaccine 1 which targets COVID-19 (2026/2027 recommended strain) injected in the upper arm. The study team and participants will know which injection they receive. Participants in Cohort 2 of this study will randomly receive 1 injection into their upper arm of either: BNT162b2 vaccine 1; BNT162b2 vaccine 2, or BNT162b2 vaccine 3 which targets COVID-19. The study team and participants will not know which injection they receive. Participants will be in the study for about 6 months and will have at least 3 study visits. Participants will record side effects and complete diaries following visit procedures. For Cohort 1 the study team will collect a nose swab and blood samples at 2 of the 3 visits. For Cohort 2 the study team will collect a nose swab and blood samples at all of the visits.

Más ensayos de BNTX

EnsayoFaseEstadoLectura de resultados
BNT164a1Fase 1/2En marcha, sin reclutarmar 2026 (real)
BNT162b2 VaccineFase 3En marcha, sin reclutarjul 2026 (prevista, ya pasada: sin actualizar en el registro)
BNT314Fase 1En marcha, sin reclutarago 2026 (real)
BNT163Fase 1En marcha, sin reclutaroct 2026 (prevista)
RO7198457 intravenousFase 2En marcha, sin reclutarnov 2026 (prevista)
BNT351Fase 1Reclutando pacientesnov 2026 (prevista)

Todos los de BNTX, en su ficha.

Ficha completa en ClinicalTrials.gov (NCT07798648), actualizada en sep 2026.