rBCG-N-RSV Vaccine in Adults Aged 60 Years and Older
Randomized, Double-blind, Phase 2 Clinical Trial Controlled With Conventional Bacillus Calmette-Guérin (BCG) Vaccine to Evaluate the Safety and Immunogenicity of a Recombinant BCG Vaccine That Expresses the Respiratory Syncytial Virus (RSV) Nucleoprotein (N) (rBCG-N-RSV) in Adults Over 60 Years of Age.
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ2
連絡先と場所
研究連絡先
研究連絡先
- 名前:Maria Moukouli
- 電話番号:+30 210 6560700
- メール:m.moukouli@pharmassist-cro.com
研究連絡先のバックアップ
- 名前:Maria Kiriakaki
- 電話番号:+30 210 6560700
- メール:m.kiriakaki@pharmassist-cro.com
研究場所
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Athens、ギリシャ
- 募集
- Sotiria Thoracic Diseases Hospital of Athens
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コンタクト:
- Nikoletta Rovina, MD
- 電話番号:+30 2107763100
- メール:nikrovina@med.uoa.gr
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参加基準
適格基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria
- Has completed the written informed consent process.
- Males or females, over 60 years of age as of the date of signature of the informed consent form.
- Has a stable state of health or controlled (health parameters within the normal range for their disease) chronic diseases that do not fall within the exclusion criteria.
- Willingness to comply with study procedures.
- No plans to move to another city in the next 6 months and willing to be contacted by the research team within the study period.
- Not participate in another research study in the previous 3 months, nor plans to participate in another research study in the next 6 months.
- Agrees to avoid elective surgery during the study.
- Willingness to receive HIV test results.
- Not having received a BCG vaccination within the last 10 years before study vaccination.
Exlusion Criteria
- Oral temperature ≥37.5°C, axillary ≥37.5°C or tympanic temperature ≥38.0°C in the last 24 hours.
- Weight less than 50 kg, as well as BMI less than 18.5 or higher than 35 kg/m2.
- History of treatment or current history of active or latent tuberculosis infection.
- History of unprotected occupational exposure to an individual with active tuberculosis in a healthcare setting within the past 6 months.
- Immunosuppressive drugs used within the previous 42 days (inhaled and topical corticosteroids are allowed).
- Received documented investigational tuberculosis vaccine at any time.
- Unstable hormonal status, i.e. subjects with any change (dose, formulation, or route) in hormone replacement therapies (including levothyroxine, insulin, estrogen, progesterone etc.) in the last 12 weeks.
- History or laboratory evidence of any possible past, present, or future immunodeficiency status, including, but not limited to, any laboratory indication of HIV-1 infection.
- Allergy to BCG vaccine or its components, as well as the existence of contraindications for BCG administration as described in the BCG prescribing information.
- Previous medical history that may compromise the safety of the study participant, including but not limited to significant impairment of lung function (such as pulmonary diffusion of carbon dioxide <80% or FEV1 ≤80%) due to tuberculosis infection or other pulmonary disease; chronic heart disease with signs of heart failure (NYHA Class II Heart Failure or more) or coronary heart disease, suspicion of progressive neurological disease; uncontrolled epilepsy, liver disease.
- Administration of attenuated vaccines within 30 days before the start of the study or 14 days for inactivated ones.
- Having received transfusions or blood products within the 6 months before the start of the study.
- Uncontrolled hypertension or systolic blood pressure greater than 160 mmHg at the beginning of the study or diastolic greater than 90 mmHg.
- Active neoplasia.
- Stage 2 or higher chronic obstructive pulmonary disease.
- Chronic bronchial asthma with systemic corticosteroids, or with a history of having presented crises that have led to an emergency consultation within the last 2 months.
- Renal disease with estimated or relative creatinine clearance ≤ 70 ml/min x 1.73 m2.
- Evidence of a new acute illness that may compromise the safety of the study participant, such as fever (oral or axillary temperature greater than or equal to 37.5°C) or suspicion of active infection.
- History or laboratory evidence of chronic viral hepatitis.
- History of alcohol or drug abuse in the last 2 years.
- Smoking more than 30 cigarettes a day, or cannabis use three or more days a week.
- History of keloid formation.
- Congenital diseases of importance, such that they weaken the basal condition of the volunteer.
- Congenital or acquired absence of the spleen.
- Coagulation disorders or known thrombocytopenia of less than 100,000 platelets/mm3.
- Having undergone chemotherapy treatment in the last 6 months.
- Generalized urticaria in the last 2 months.
- History of hereditary or acquired angioneurotic edema.
- Any previous medical condition that the investigator considers may compromise the safety of the subject in the study.
- Not being available for all study visits (both face-to-face and by telephone) and specific instructions as appropriate (fasting, abstaining from intense physical exercise during the 24 hours before the study visits and during the 72 hours after vaccination).
- Pregnant women or women of childbearing potential (WOCBP) who are unable or unwilling to utilize appropriate methods of contraception during the study.
- Breast-feeding women.
- Male with heterosexual sexual activity with WOCBP who do not agree to use adequate contraception.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:防止
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
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実験的:rBCG-N-RSV vaccine
rBCG-N-RSV is a live-attenuated vaccine of Mycobacterium bovis bacillus Calmette-Guerin (BCG) modified to heterologously and constitutively express the RSV nucleoprotein (N). The clinical formulation with this bacterium has been produced under strict quality and safety standards using current Good Manufacturing Practices (cGMP) in the United States of America (USA). Pharmaceutical form: Lyophilisate for solution for injection Medicinal product characteristics: Immunological Route of administration: Intradermal use Maximum duration of treatment: 1 Day Maximum daily dose allowed: 0.1 Daily dose unit of measure: CFU/ml colony forming unit(s)/millilitre Maximum total dose allowed: 0.1 Total dose unit of measure: CFU/ml colony forming unit(s)/millilitre |
Intradermal vaccination with rBCG-N-RSV that expresses the N protein of the respiratory syncytial virus (RSV)
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アクティブコンパレータ:Mycobacterium bovis bacillus Calmette-Guerin (BCG)
BCG is a cryo-lyophilized vaccine of an attenuated strain of Mycobacterium bovis BCG, used for active immunization against tuberculosis. It is currently administered in numerous countries worldwide according to national immunization plans. Medicinal product characteristics: Immunological Route of administration: Intradermal use Maximum duration of treatment: 1 Day Maximum daily dose allowed: 0.1 Daily dose unit of measure: CFU/ml colony forming unit(s)/millilitre Maximum total dose allowed: 0.1 Total dose unit of measure: CFU/ml colony forming unit(s)/millilitre |
Intradermal vaccination with conventional BCG (BCG-WT).
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この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
時間枠 |
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Occurrence, intensity, and duration of the local solicited AEs (evolution of the "flare-up") until the generation of the scar
時間枠:From vaccination through 180 days post-vaccination
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From vaccination through 180 days post-vaccination
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Occurrence, intensity and duration of unsolicited AEs during the 6-month follow-up.
時間枠:From vaccination through 180 days post-vaccination
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From vaccination through 180 days post-vaccination
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Occurrence of AEs during the 6-month follow-up duration.
時間枠:From vaccination through 180 days post-vaccination
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From vaccination through 180 days post-vaccination
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Alterations to the hemogram and/or biochemical profile at 30- and 180- days post vaccination compared to pre-vaccination profile
時間枠:Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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Production of IFN-γ and IL-2 by T cells upon exposure to purified protein derivative (PPD) mycobacterial antigen via ELISPOT 7 days prior vaccination and 30- and 180-days post vaccination.
時間枠:Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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Production of IFN-γ and IL-2 by T cells upon exposure to recombinant RSV nucleoprotein antigen via ELISPOT 7 days prior vaccination and 30- and 180-days post vaccination
時間枠:Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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二次結果の測定
二次結果の測定
結果測定 |
時間枠 |
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Presence and titers of serum IgG antibodies against Purified Protein Derived Mycobacterial antigen (PPD) via ELISA
時間枠:Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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Presence and titers of serum IgG against RSV nucleoprotein via ELISA.
時間枠:Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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その他の成果指標
その他の成果指標
結果測定 |
時間枠 |
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Cases of symptomatic RSV infection confirmed by RT-qPCR detection in respiratory specimens from 14 days to 6 months after vaccination.
時間枠:From day 14 to 6 months post-vaccination
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From day 14 to 6 months post-vaccination
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Cases of hospitalization/intensive care unit admission and/or death in participants with RSV infection confirmed by RT-qPCR in vaccinated subjects from 14 days to 6 months postvaccination
時間枠:From day 14 to 6 months post-vaccination
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From day 14 to 6 months post-vaccination
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Increase in the percentage of specific CD4+ and CD8+ T cells that express AIM and memory markers via flow cytometry in the peripheral blood of a subgroup of participants that receive the control and the study vaccine.
時間枠:Day 30 and day 180 post-vaccination
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Day 30 and day 180 post-vaccination
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協力者と研究者
協力者
協力者
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- rBCG-N-RSV 002GR
- 2023 (米国 NIH グラント/契約:GRAMMY Museum Foundation)
- 2023-509048-80-01 (Ctis)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
IPD プランの説明
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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