Trials (Jul 2023)

Optimising DTwP-containing vaccine infant immunisation schedules (OptImms) — a protocol for two parallel, open-label, randomised controlled trials

  • Sarah Kelly,
  • Xinxue Liu,
  • Katherine Theiss-Nyland,
  • Merryn Voysey,
  • Sarah Murphy,
  • Grace Li,
  • Mary Nyantaro,
  • Meeru Gurung,
  • Sudha Basnet,
  • Bhishma Pokhrel,
  • Sanjeev M. Bijukchhe,
  • Agnes Eordogh,
  • Ben Gombe,
  • Ayoub Kakande,
  • Simon Kerridge,
  • Geofrey Kimbugwe,
  • Sylvia Kusemererwa,
  • Lawrence Lubyayi,
  • Henry Luzze,
  • Olga Mazur,
  • Yama F. Mujadidi,
  • Shamim Nabukenya,
  • Walter-Rodney Nagumo,
  • Tryphena Nareeba,
  • Rabiullah Noristani,
  • Peter O’Reilly,
  • Andrew Roberts,
  • Ganesh Shah,
  • Sonu Shrestha,
  • Laxman P. Shrestha,
  • Surya B. Thapa,
  • Freddie M. Kibengo,
  • Arun K. Sharma,
  • Alison Elliott,
  • Shrijana Shrestha,
  • Andrew J. Pollard

DOI
https://doi.org/10.1186/s13063-023-07477-9
Journal volume & issue
Vol. 24, no. 1
pp. 1 – 9

Abstract

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Abstract Background Universal immunisation is the cornerstone of preventive medicine for children, The World Health Organisation (WHO) recommends diphtheria-tetanus-pertussis (DTP) vaccine administered at 6, 10 and 14 weeks of age as part of routine immunisation. However, globally, more than 17 unique DTP-containing vaccine schedules are in use. New vaccines for other diseases continue to be introduced into the infant immunisation schedule, resulting in an increasingly crowded schedule. The OptImms trial will assess whether antibody titres against pertussis and other antigens in childhood can be maintained whilst adjusting the current Expanded Programme on Immunisation (EPI) schedule to provide space for the introduction of new vaccines. Methods The OptImms studies are two randomised, five-arm, non-inferiority clinical trials in Nepal and Uganda. Infants aged 6 weeks will be randomised to one of five primary vaccination schedules based on age at first DTwP-vaccination (6 versus 8 weeks of age), number of doses in the DTwP priming series (two versus three), and spacing of priming series vaccinations (4 versus 8 weeks). Additionally, participants will be randomised to receive their DTwP booster at 9 or 12 months of age. A further sub-study will compare the co-administration of typhoid vaccine with other routine vaccines at one year of age. The primary outcome is anti-pertussis toxin IgG antibodies measured at the time of the booster dose. Secondary outcomes include antibodies against other vaccine antigens in the primary schedule and their safety. Discussion These data will provide key data to inform policy decisions on streamlining vaccination schedules in childhood. Trial registrations ISRCTN12240140 (Nepa1, 7th January 2021) and ISRCTN6036654 (Uganda, 17th February 2021).

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