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Immunogenicity and Safety of a Hexavalent DTwP-IPV-HB-PRP~T Vaccine Versus Separate DTwP-HB-PRP~T, bOPV, and IPV Vaccines Administered at 2, 4, 6 Months of Age Concomitantly With Rotavirus and Pneumococcal Conjugate Vaccines in Healthy Infants in Thailand.
Sanchez, Leilani; Rungmaitree, Supattra; Kosalaraksa, Pope; Jantarabenjakul, Watsamon; Leclercq, Julie; Yaiprayoon, Yuvadee; Midde, Venkata Jayanth; Varghese, Kucku; Mangarule, Somnath; Noriega, Fernando.
  • Sanchez L; From the Sanofi, Taguig City, Philippines.
  • Rungmaitree S; Department of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
  • Kosalaraksa P; Department of Pediatrics, Faculty of Medicine, Khon Kaen University, Thailand.
  • Jantarabenjakul W; Department of Pediatrics, King Chulalongkorn Memorial Hospital, Bangkok, Thailand.
  • Leclercq J; Department of Pediatrics, Center of Excellence for Pediatric Infectious Diseases and Vaccines, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
  • Yaiprayoon Y; AIXIAL, Boulogne-Billancourt, France.
  • Midde VJ; Sanofi, Thailand.
  • Varghese K; Sanofi Healthcare India Private Limited, India.
  • Mangarule S; Sanofi, Swiftwater, Pennsylvania, USA.
  • Noriega F; Sanofi, Marcy l'Etoile, France.
Pediatr Infect Dis J ; 42(8): 711-718, 2023 08 01.
Article en En | MEDLINE | ID: mdl-37257121
ABSTRACT

BACKGROUND:

This study investigated the immunogenicity and safety of a fully liquid, hexavalent, diphtheria (D)-tetanus (T)-whole-cell pertussis (wP)-inactivated poliovirus (IPV)-hepatitis B (HB)- Haemophilus influenzae b (PRP-T) vaccine compared to licensed DTwP-HB-PRP~T, IPV, and bivalent oral poliovirus (bOPV) vaccines following co-administration with other pediatric vaccines [pneumococcal conjugate vaccine (PCV13) and rotavirus vaccine].

METHODS:

Phase III, randomized, open-label study in Thailand. Healthy infants received DTwP-IPV-HB-PRP~T at 2, 4 and 6 months of age (N = 228), or DTwP-HB-PRP~T and bOPV (2, 4 and 6 months of age) and IPV (4 months of age) (N = 231). All participants received PCV13 (2, 4 and 6 months of age) and rotavirus vaccine (2 and 4 months of age). Immunogenicity for all antigens was assessed using validated assays, and noninferiority post-third dose was evaluated for anti-D, anti-T, anti-pertussis [anti-pertussis toxin (anti-PT) and anti-fimbriae 2/3 (anti-FIM)], anti-polio 1, 2, 3, anti-HB, and anti-PRP~T. Safety was assessed using parental reports.

RESULTS:

Noninferiority was demonstrated for each antigen, and overall noninferiority of DTwP-IPV-HB-PRP~T versus DTwP-HB-PRP~T+bOPV+IPV was concluded. Similarity in each group was observed for the GMC ratio for antirotavirus antibodies (20.9 and 17.3, respectively) and anti-PCV13 antibodies (range 8.46-32.6 and 7.53-33.1, respectively). Two serious adverse events were related to DTwP-IPV-HB-PRP~T (febrile convulsion and acute febrile illness) and 1 was related to DTwP-HB-PRP~T+bOPV+IPV (febrile seizure), but overall there were no safety concerns with similar rates of participants experiencing solicited (99.1% and 98.3%) and unsolicited (19.3% and 19.5%) adverse events in each group.

CONCLUSIONS:

This study confirmed the suitability of DTwP-IPV-HB-PRP~T primary series vaccination in combination with rotavirus and PCV13 vaccines.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacuna Antipolio de Virus Inactivados / Vacuna contra Difteria, Tétanos y Tos Ferina / Vacunas contra Hepatitis B / Vacunas Combinadas / Vacunas contra Haemophilus / Vacunas contra Rotavirus Tipo de estudio: Clinical_trials Límite: Humans / Infant País como asunto: Asia Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Vacuna Antipolio de Virus Inactivados / Vacuna contra Difteria, Tétanos y Tos Ferina / Vacunas contra Hepatitis B / Vacunas Combinadas / Vacunas contra Haemophilus / Vacunas contra Rotavirus Tipo de estudio: Clinical_trials Límite: Humans / Infant País como asunto: Asia Idioma: En Año: 2023 Tipo del documento: Article