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rBCG-N-RSV Vaccine in Adults Aged 60 Years and Older

14 septembre 2026 mis à jour par: Biothervax SpA

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.

This Phase 2 clinical study will evaluate the safety of the rBCG-N-RSV vaccine compared to conventional BCG in adults older than 60 years. It will also compare the cellular anti-mycobacterial immune response of both vaccines in adults older than 60 years and characterize the cellular immune response against RSV nucleoprotein (N) generated by the rBCG-N-RSV vaccine in adults older than 60 years as compared to the response induced by the conventional BCG.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

200

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Lieux d'étude

      • Athens, Grèce
        • Recrutement
        • Sotiria Thoracic Diseases Hospital of Athens
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La description

Inclusion Criteria

  1. Has completed the written informed consent process.
  2. Males or females, over 60 years of age as of the date of signature of the informed consent form.
  3. 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.
  4. Willingness to comply with study procedures.
  5. 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.
  6. Not participate in another research study in the previous 3 months, nor plans to participate in another research study in the next 6 months.
  7. Agrees to avoid elective surgery during the study.
  8. Willingness to receive HIV test results.
  9. Not having received a BCG vaccination within the last 10 years before study vaccination.

Exlusion Criteria

  1. Oral temperature ≥37.5°C, axillary ≥37.5°C or tympanic temperature ≥38.0°C in the last 24 hours.
  2. Weight less than 50 kg, as well as BMI less than 18.5 or higher than 35 kg/m2.
  3. History of treatment or current history of active or latent tuberculosis infection.
  4. History of unprotected occupational exposure to an individual with active tuberculosis in a healthcare setting within the past 6 months.
  5. Immunosuppressive drugs used within the previous 42 days (inhaled and topical corticosteroids are allowed).
  6. Received documented investigational tuberculosis vaccine at any time.
  7. 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.
  8. 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.
  9. Allergy to BCG vaccine or its components, as well as the existence of contraindications for BCG administration as described in the BCG prescribing information.
  10. 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.
  11. Administration of attenuated vaccines within 30 days before the start of the study or 14 days for inactivated ones.
  12. Having received transfusions or blood products within the 6 months before the start of the study.
  13. Uncontrolled hypertension or systolic blood pressure greater than 160 mmHg at the beginning of the study or diastolic greater than 90 mmHg.
  14. Active neoplasia.
  15. Stage 2 or higher chronic obstructive pulmonary disease.
  16. 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.
  17. Renal disease with estimated or relative creatinine clearance ≤ 70 ml/min x 1.73 m2.
  18. 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.
  19. History or laboratory evidence of chronic viral hepatitis.
  20. History of alcohol or drug abuse in the last 2 years.
  21. Smoking more than 30 cigarettes a day, or cannabis use three or more days a week.
  22. History of keloid formation.
  23. Congenital diseases of importance, such that they weaken the basal condition of the volunteer.
  24. Congenital or acquired absence of the spleen.
  25. Coagulation disorders or known thrombocytopenia of less than 100,000 platelets/mm3.
  26. Having undergone chemotherapy treatment in the last 6 months.
  27. Generalized urticaria in the last 2 months.
  28. History of hereditary or acquired angioneurotic edema.
  29. Any previous medical condition that the investigator considers may compromise the safety of the subject in the study.
  30. 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).
  31. Pregnant women or women of childbearing potential (WOCBP) who are unable or unwilling to utilize appropriate methods of contraception during the study.
  32. Breast-feeding women.
  33. Male with heterosexual sexual activity with WOCBP who do not agree to use adequate contraception.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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)
Comparateur actif: 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).

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
Occurrence, intensity, and duration of the local solicited AEs (evolution of the "flare-up") until the generation of the scar
Délai: From vaccination through 180 days post-vaccination
From vaccination through 180 days post-vaccination
Occurrence, intensity and duration of unsolicited AEs during the 6-month follow-up.
Délai: From vaccination through 180 days post-vaccination
From vaccination through 180 days post-vaccination
Occurrence of AEs during the 6-month follow-up duration.
Délai: From vaccination through 180 days post-vaccination
From vaccination through 180 days post-vaccination
Alterations to the hemogram and/or biochemical profile at 30- and 180- days post vaccination compared to pre-vaccination profile
Délai: Day 30 and day 180 post-vaccination
Day 30 and day 180 post-vaccination
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.
Délai: Day 30 and day 180 post-vaccination
Day 30 and day 180 post-vaccination
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
Délai: Day 30 and day 180 post-vaccination
Day 30 and day 180 post-vaccination

Mesures de résultats secondaires

Mesure des résultats
Délai
Presence and titers of serum IgG antibodies against Purified Protein Derived Mycobacterial antigen (PPD) via ELISA
Délai: Day 30 and day 180 post-vaccination
Day 30 and day 180 post-vaccination
Presence and titers of serum IgG against RSV nucleoprotein via ELISA.
Délai: Day 30 and day 180 post-vaccination
Day 30 and day 180 post-vaccination

Autres mesures de résultats

Mesure des résultats
Délai
Cases of symptomatic RSV infection confirmed by RT-qPCR detection in respiratory specimens from 14 days to 6 months after vaccination.
Délai: From day 14 to 6 months post-vaccination
From day 14 to 6 months post-vaccination
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
Délai: From day 14 to 6 months post-vaccination
From day 14 to 6 months post-vaccination
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.
Délai: Day 30 and day 180 post-vaccination
Day 30 and day 180 post-vaccination

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

14 septembre 2026

Achèvement primaire (Estimé)

7 septembre 2027

Achèvement de l'étude (Estimé)

31 décembre 2027

Dates d'inscription aux études

Première soumission

2 août 2026

Première soumission répondant aux critères de contrôle qualité

5 août 2026

Première publication (Réel)

13 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

15 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

14 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

INDÉCIS

Description du régime IPD

It has not been decided where the results of the study will be published.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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