Trial to Describe the Safety, Tolerability, and Immunogenicity of Trumenba When Administered to Immunocompromised Participants ≥10 Years of Age

PHASE4CompletedINTERVENTIONAL
Enrollment

53

Participants

Timeline

Start Date

August 18, 2021

Primary Completion Date

September 6, 2023

Study Completion Date

September 6, 2023

Conditions
Meningococcal Vaccine
Interventions
BIOLOGICAL

Trumenba

Bivalent recombinant lipoprotein 2086 vaccine

Trial Locations (14)

33343

Mersin Universitesi Tip Fakultesi Hastanesi, Mersin

61300

Fakultni Nemocnice Brno - Detska Nemocnice - Klinika Detskych Infekcnich Nemoci Center 3, Brno

613 00

Fakultni Nemocnice Brno - Detska Nemocnice - Klinika Detskych Infekcnich Nemoci Center 3, Brno

150 06

Fakultni nemocnice v Motole, Prague

85-048

IN-VIVO Sp. z o.o., Bydgoszcz

30-348

Centrum Badań Klinicznych Jagiellońskie Centrum Innowacji sp. z o.o., Krakow

00-728

WIP Warsaw IBD Point Profesor Kierkus, Warsaw

01-809

Szpital Bielański im. Ks. Jerzego Popiełuszki SPZOZ, Warsaw

01120

Baskent Universitesi Dr. Turgut Noyan Adana Uygulama ve Arastirma Merkezi, Adana

Baskent Universitesi Dr. Turgut Noyan Adana Uygulama ve Arastirma Merkezi, Adana

Unknown

Baskent Universitesi Dr. Turgut Noyan Adana Uygulama ve Arastirma Merkezi, Adana

01130

Acibadem Adana Hastanesi, Adana

01240

Baskent Universitesi Dr. Turgut Noyan Adana Uygulama ve Arastirma Merkezi, Adana

06230

Hacettepe Universitesi Tip Fakultesi, Ankara

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT04893811 - Trial to Describe the Safety, Tolerability, and Immunogenicity of Trumenba When Administered to Immunocompromised Participants ≥10 Years of Age | Biotech Hunter | Biotech Hunter