MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1016/j.vaccine.2020.03.014

Медицинская библиотека · Vaccine · 2020

Immunogenicity and safety of the RTS,S/AS01 malaria vaccine co-administered with measles, rubella and yellow fever vaccines in Ghanaian children: A phase IIIb, multi-center, non-inferiority, randomized, open, controlled trial.

Asante Kwaku Poku, Ansong Daniel, Kaali Seyram, Adjei Samuel, Lievens Marc, Nana Badu Lydia, Agyapong Darko Prince, Boakye Yiadom Buabeng Patrick, Boahen Owusu, Maria Rettig Theresa, Agutu Clara, Benard Ekow Harrison Samuel, Ntiamoah Yaw, Adomako Anim Japhet, Adeniji Elisha, Agordo Dornudo Albert, Gvozdenovic Emilia, Dosoo David, Sambian David, Owusu-Boateng Harry, Ato Wilson Elvis, Prempeh Frank, Vandoolaeghe Pascale, Schuerman Lode, Owusu-Agyei Seth, Agbenyega Tsiri, Ofori-Anyinam Opokua

Клиническое исследование III фазыСтатьяМногоцентровое исследованиеРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

To optimize vaccine implementation visits for young children, it could be efficient to administer the first RTS,S/AS01 malaria vaccine dose during the Expanded Programme on Immunization (EPI) visit at 6 months of age together with Vitamin A supplementation and the third RTS,S/AS01 dose on the same day as yellow fever (YF), measles and rubella vaccines at 9 months of age. We evaluated the safety and immunogenicity of RTS,S/AS01 when co-administered with YF and combined measles-rubella (MR) vaccines.

METHODS

In this phase 3b, open-label, controlled study (NCT02699099), 709 Ghanaian children were randomized (1:1:1) to receive RTS,S/AS01 at 6, 7.5 and 9 months of age, and YF and MR vaccines at 9 or 10.5 months of age (RTS,S coad and RTS,S alone groups, respectively). The third group received YF and MR vaccines at 9 months of age and will receive RTS,S/AS01 at 10.5, 11.5 and 12.5 months of age (Control group). All children received Vitamin A at 6 months of age. Non-inferiority of immune responses to the vaccine antigens was evaluated 1 month following co-administration versus RTS,S/AS01 or EPI vaccines (YF and MR vaccines) alone using pre-defined non-inferiority criteria. Safety was assessed until Study month 4.5.

RESULTS

Non-inferiority of antibody responses to the anti-circumsporozoite and anti-hepatitis B virus surface antigens when RTS,S/AS01 was co-administered with YF and MR vaccines versus RTS,S/AS01 alone was demonstrated. Non-inferiority of antibody responses to the measles, rubella, and YF antigens when RTS,S/AS01 was co-administered with YF and MR vaccines versus YF and MR vaccines alone was demonstrated. The safety profile of all vaccines was clinically acceptable in all groups.

CONCLUSIONS

RTS,S/AS01 can be co-administered with Vitamin A at 6 months and with YF and MR vaccines at 9 months of age during EPI visits, without immune response impairment to any vaccine antigen or negative safety effect.

Для цитирования: Asante Kwaku Poku, Ansong Daniel, Kaali Seyram, Adjei Samuel, Lievens Marc, Nana Badu Lydia, Agyapong Darko Prince, Boakye Yiadom Buabeng Patrick, Boahen Owusu, Maria Rettig Theresa, Agutu Clara, Benard Ekow Harrison Samuel, Ntiamoah Yaw, Adomako Anim Japhet, Adeniji Elisha, Agordo Dornudo Albert, Gvozdenovic Emilia, Dosoo David, Sambian David, Owusu-Boateng Harry, Ato Wilson Elvis, Prempeh Frank, Vandoolaeghe Pascale, Schuerman Lode, Owusu-Agyei Seth, Agbenyega Tsiri, Ofori-Anyinam Opokua. Immunogenicity and safety of the RTS,S/AS01 malaria vaccine co-administered with measles, rubella and yellow fever vaccines in Ghanaian children: A phase IIIb, multi-center, non-inferiority, randomized, open, controlled trial.. Vaccine. 2020. DOI: 10.1016/j.vaccine.2020.03.014.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.