A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase IV Clinical Trial to Evaluate the Immunogenicity and Safety of a Live Attenuated Herpes Zoster Vaccine in Adults Aged 40 Years and Older

Обзор

To evaluate the immunogenicity 42 days after vaccination with the live attenuated herpes zoster vaccine. To evaluate the safety of the live attenuated herpes zoster vaccine.

Вмешательства

• Биопрепарат Herpes Zoster Vaccine, Live
  assigned to the vaccine group and placebo group in a 2:1 ratio.
• Биопрепарат Placebo
  assigned to the vaccine group and placebo group in a 2:1 ratio.

Первичные конечные точки

• Immunogenicity: [Срок оценки: Day 0 and Day 42]
• Immunogenicity: [Срок оценки: Day 0 and Day 42]
• Immunogenicity: [Срок оценки: Day 0 and Day 42]
• Immunogenicity: [Срок оценки: Day 0 and Day 42]

Вторичные конечные точки (1)

• Adverse Events [Срок оценки: 42 days]

Критерии участия

Критерии включения

• Age ≥40 years on enrollment day；
• The informed consent of the subject can be obtained and signed；
• The subjects themselves were able to complete the trial in accordance with the requirements of the clinical trial protocol；
• Armpit body temperature ≤37.0℃ on the day of enrollment.

Критерии исключения

• People who are immune deficient or immunosuppressed due to certain diseases or treatments. Causes of immunodeficiency or immunosuppression may include, but are not limited to, primary or acquired immunodeficiency conditions, such as AIDS or other diseases caused by viral infection; Leukemia, lymphoma, or other malignancies affecting the bone marrow or lymphatic system; Being treated for immunosuppression; Being treated with radiation/chemotherapy for a tumor；
• Do not use in persons with a history of allergic reaction to any of the components contained in this product；
• Those who are in the acute stage of acute infection and chronic infection should postpone the vaccination of this product；
• Premenopausal women who tested positive for pregnancy, pregnant women, breastfeeding women, or those who planned to have a baby within 6 months；
• If this product and other injectable live attenuated vaccines are not administered at the same time, the interval should be at least 28 days；
• Treatment with whole blood, plasma, or immunoglobulin is given within 5 months or 3 weeks prior to vaccination；
• Received another investigational drug within 1 month prior to receiving the investigational vaccine/placebo, or is participating in another clinical trial, or plans to use it during the study；
• Taking or about to take salicylate drugs, including aspirin and difluorosalicylic acid；
• Patients with abnormal blood pressure that cannot be controlled by medication (systolic blood pressure ≥160mmHg and/or diastolic blood pressure ≥100mmHg)；
• Previous vaccinations against chickenpox or shingles (including use of registered products or participation in clinical trials of chickenpox or shingles vaccine)；
• Any situation that the investigator considers likely to affect the evaluation of the trial。

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Четверное слепое

Основная цель

Профилактика

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT06961721 · PFDP20241008

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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