A Study Evaluating the Safety and Immunogenicity of MVA Strain Monkeypox Attenuated Live Vaccine

Официальное название

A Randomized, Double-blind, Placebo-controlled Phase I Clinical Trial Evaluating the Safety and Immunogenicity of MVA Strain Monkeypox Attenuated Live Vaccine for Individuals Aged 18 and Above

Обзор

This is a randomized, double blinded, controlled phase I clinical study. To evaluate the safety and immunogenicity of receiving two doses of MVA strain monkeypox attenuated live vaccine in individuals aged 18 years and above.

Подробное описание

This is a randomized, double blinded, controlled phase I clinical study. The study plans to recruit 120 participants aged 18 years and above. The experimental vaccine MVA strain monkeypox attenuated live vaccine has two different doses (low dose and high dose). The ratio of low-dose experimental group, high-dose experimental group, and placebo group is 1:1:1. Participants will be divided into three groups: healthy individuals, men who have sex with men, and HIV infected individuals, with a ratio of 2:1:1. Different groups will be divided into individuals with a history of vaccination against smallpox and those without a history of immunization, based on whether each population has a history of vaccination against smallpox. Each participant will receive one dose of the experimental vaccine or placebo on day 0 and day 28, respectively.

Вмешательства

• Биопрепарат MVA strain monkeypox attenuated live vaccine (low dose)
  Low dose MVA strain monkeypox attenuated live vaccine
• Биопрепарат MVA strain monkeypox attenuated live vaccine (high dose)
  High dose MVA strain monkeypox attenuated live vaccine
• Другое Placebo
  Vaccine excipient

Первичные конечные точки

• Immediate adverse events [Срок оценки: 60 minutes after each dose of vaccination]
• Solicited Adverse Events [Срок оценки: 14 days after each dose of vaccination]
• Unsolicited Adverse Events [Срок оценки: 28 or 30 days after each dose of vaccination]
• Abnormal incidence rate of electrocardiogram [Срок оценки: 14 days after each dose of vaccination]
• Serious Adverse Events (SAE) [Срок оценки: 12 months after the last dose]
• Adverse Event of Special Interest (AESI) [Срок оценки: 12 months after the last dose]

Критерии участия

Критерии включения

• On the day of enrollment, individuals aged 18 years or older with a history of smallpox vaccination must have been born before 1980;
• Can provide legal proof of identity;
• Be able to understand the experimental procedure and sign a written informed consent form, expressing agreement to participate in the experiment;
• Be able to participate in all planned follow-up visits and comply with all trial procedures (such as completing diary/contact cards and being able to return for visits);
• On the day of enrollment, the body temperature was less than 37.3 ℃ (axillary temperature);
• Men and women of childbearing age who have no plans to have children within 6 months and agree to take effective contraceptive measures within 6 months after receiving the experimental vaccine.

Критерии исключения

• Individuals with a history of smallpox, monkeypox, or close contact with monkeypox in the past;
• Individuals who are allergic to any ingredients of eggs, vaccines, or substances used in production processes, or have a history of other severe allergies;
• Use immunoglobulin and/or any blood products within 3 months prior to administering the trial vaccine, or plan to use them during the trial period;
• Currently using salicylate drugs or planning long-term use during the trial period;
• Have used any experimental or unregistered products within one month prior to administering the trial vaccine, or plan to use them during the trial period;
• Administer inactivated vaccine within 14 days before administering the experimental vaccine or attenuated live vaccine within 30 days before administering the experimental vaccine;
• Chronic disease patients are in the acute or progressive phase of chronic disease;
• Long term use of immunosuppressants or other immunomodulatory drugs within 6 months prior to vaccination with the experimental vaccine;
• Having undergone chemotherapy or radiation therapy or organ and bone marrow transplantation related treatments for cancer or other diseases;
• Diseases or medical measures that lead to immune dysfunction, such as congenital immunodeficiency, organ and bone marrow transplantation, leukemia, lymphoma, Hodgkin's disease, multiple myeloma or malignant tumors, etc;
• Moderate or severe acute illness/infection, or febrile illness on the day of vaccination;
• Individuals with a history of thrombocytopenia or other coagulation disorders may be contraindicated for subcutaneous injection;
• Suffering from serious cardiovascular disease, serious liver and kidney disease, and diabetes that cannot be controlled by drugs;
• Previous history of mental or neurological disorders or family history;
• Currently suffering from various infectious, suppurative, and allergic skin diseases;
• Women of childbearing age: pregnant or lactating, or with a positive blood pregnancy test;
• Plan to move before the end of the trial or leave the local area for a long time during the scheduled trial visit;
• Abnormal blood routine, blood biochemistry, urine routine, electrocardiogram or heart disease related indicators before vaccination (except for minor abnormalities judged by doctors to have no clinical significance);
• Researchers believe that any situation that may affect the evaluation of the experiment;
• Active tuberculosis patients;
• For HIV infected individuals, the plasma HIV-1 RNA level during screening should be ≥ 200 copies/mL, or positive test for hepatitis B, hepatitis C and syphilis;
• For healthy people and men and women who have sex with each other, hepatitis B, hepatitis C, syphilis and HIV) are positive;
• Individuals who experience severe allergic reactions after the first dose of vaccination;
• Serious adverse events that are definitely related to the first dose of vaccination;
• For those who are newly discovered or occur after the first dose of vaccination and do not meet the inclusion criteria or the exclusion criteria for the first dose, the researcher shall determine whether to continue participating in 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

Китай · 1 центр

• Henan Infectious Disease Hospital — Чжэнчжоу

Идентификаторы

NCT: NCT06771479 · SIBP-V08-Ⅰ

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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