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RENEW-SHCS: Safety and Immunogenicity of a Recombinant HIV Env Protein Vaccine in ARV-treated Adults Living With HIV in the SHCS (RENEW-SHCS)

10 septembre 2026 mis à jour par: University of Zurich

RENEW-SHCS: A Phase 1 Open-label Clinical Trial to Evaluate the Safety and Immunogenicity of Recombinant HIV-1 Env Protein BG505 SOSIP.GT1.1 gp140 Vaccine, Adjuvanted, in ARV-treated Adults Living With HIV Enrolled in the SHCS and to Restimulate and Newly Prime Antibody Responses.

A vaccine trial in which people with HIV-1 participating in the Swiss HIV Cohort Study will receive a HIV-specific vaccine to stimulate antibodies against HIV while continuing their standard antiretroviral therapy

Aperçu de l'étude

Description détaillée

Vaccination of people with HIV (PWH) on suppressive antiretroviral therapy (ART) represents a novel approach for evaluating candidate broadly neutralizing antibody (bnAb) immunogens for preventive and therapeutic HIV vaccines. RENEW-SHCS is a phase I, open-label, non-randomized vaccination trial evaluating a single dose of the recombinant germline-targeting envelope trimer BG505 SOSIP.v4.1-GT1.1 (GT1.1), adjuvanted with 3M052-AF and Aluminum hydroxide (alum), in PWH on suppressive ART enrolled from the Swiss HIV Cohort Study. Participants were previously classified as bnAb or non-neutralizing antibody (nnAb) inducers, with a target enrollment of 15 per group, and are monitored for safety and immunogenicity for 24 weeks while continuing standard ART

Type d'étude

Interventionnel

Inscription (Estimé)

30

Phase

  • La phase 1

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.

Lieux d'étude

    • Canton of Bern
      • Bern, Canton of Bern, Suisse, 3010
        • Inselspital Bern
    • Canton of Zurich
      • Zurich, Canton of Zurich, Suisse, 8091
        • University Hospital Zurich

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

Non

La description

Inclusion Criteria:

  • Ability and willingness to provide informed consent.
  • Age ≥18 years at time of consent
  • People with HIV (PWH) with confirmed HIV-1 infection as documented by medical records and enrolled in the SHCS.
  • SHCS participants with known bnAb inducer- and non-neutralizing Ab inducer (nnAb inducer) status. (Note: Information on bnAb/nnAb status is available through SHCS-linked research prior to recruitment and has been obtained from analysis of SHCS biobanked plasma samples from off-ART and/or on-ART timepoints. Based on this information participant will be classified into bnAb inducers and nnAb inducers.)
  • On suppressive ART with plasma HIV-1 RNA <50 copies/ml for at least 1 year prior to screening. [Note: Intermittent blips (HIV-1 RNA between 50-200 copies) documented in prior years on ART are allowed but viral load at screening must be <50 copies. No switch to a novel ART regimen allowed 1 month before IMP administration. Switching from TDF to TAF and vice versa is not considered as switch to a novel regimen.]
  • CD4+ cell count > 250 cells/mm3 or CD4+ cell % ≥ 15% at screening (- 90 days prior to IMP administration)
  • At screening: Absolute neutrophil count (ANC) ≥ 750/mm3
  • At screening: Platelets ≥ 100,000/mm3
  • At screening: Alanine aminotransferase (ALT) < 2.5 x upper limit of normal (ULN) based on the institutional normal range
  • At screening: Haemoglobin (Hgb):

    • ≥ 10.0 g/dL for volunteers who were assigned female sex at birth (AFAB)
    • ≥ 11.0 g/dL for cisgender volunteers who were assigned male sex at birth (AMAB) and for transgender men who have been on hormone therapy for more than 6 consecutive months
    • ≥ 11.0 g/dL for transgender women who have been on hormone therapy for more than 6 consecutive months
    • For transgender volunteers who have been on hormone therapy for less than 6 consecutive months, determine Hgb eligibility based on their sex assigned at birth.

Persons of pregnancy potential

  • Must have a negative beta human chorionic gonadotropin (β-HCG) pregnancy test (urine or serum) on day 0 before IMP administration.
  • All participants born female who are engaging in sexual activity that could lead to pregnancy must commit to use of an effective method of contraception from 21 days before IMP administration to week 24 of the study.
  • Effective contraception includes condoms (male or female) with or without spermicide, diaphragm or cervical cap with spermicide, intrauterine device, hormonal contraception, including contraceptive implant or injectable, oral contraception, successful vasectomy in the male partner.
  • Participants born female do not have to use birth control if they are not engaging in sexual activity that could lead to pregnancy or are not of reproductive potential such as having undergone hysterectomy, bilateral oophorectomy, or tubal ligation, postmenopausal (amenorrhea for at least 1 year), surgically sterile.

Exclusion Criteria:

  • • Presence of other, HIV-unrelated, immunosuppression considered as relevant by the site investigator (e.g. a daily steroid intake of ≥20mg for 3 months is considered clinically relevant)

    • Ongoing signs and symptoms of a febrile illness at the time of the vaccination (temperature > 37.5°, and e.g. flu-like or other symptoms of a febrile illness)
    • Reduced health status due to other illnesses, which would not allow to participate in this study.
    • Volunteer who is pregnant or breast-feeding
    • Previous receipt of any anti-HIV monoclonal antibody or HIV vaccine.
    • Receipt of a non-HIV experimental vaccine(s) received within the last 6 months before IMP administration. Exceptions include vaccines that have subsequently undergone licensure or Emergency Use Authorization (EUA) by the FDA, World Health Organization (WHO) emergency use listing (EUL), Swissmedic licensure, European Medicines Agency (EMA) licensure.
    • Receipt of any other vaccine within 28 days prior to IMP administration (d0)
    • Is currently participating in or has participated in a clinical study with an investigational compound or device from in the last 45 days prior to Day 0 and throughout the study treatment period.
    • History of serious reaction (e.g., hypersensitivity, anaphylaxis) to any vaccine or component of the IMP
    • Asplenia or functional asplenia
    • Site investigator concern for difficulty with venous access based on clinical history and physical examination

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: Autre
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Single vaccination with recombinant BG505 SOSIP.GT1.1 gp140 vaccine
The vaccination with the HIV-1 envelope protein BG505 SOSIP.GT1.1 gp140 will be administered on Day 0 in selected PLWH with and without prior broadly neutralizing HIV-1 antibody activity.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Sécurité - EI non sollicités de grade 2 ou supérieur
Délai: 28 jours
Proportion de volontaires présentant des événements indésirables (EI) non sollicités de grade 2 ou plus, y compris les paramètres de laboratoire de sécurité (biochimiques, hématologiques), à partir du jour de chaque administration IP jusqu'à 28 jours après chaque administration IP
28 jours
Safety - reactogenicity
Délai: 7 days
Proportion of volunteers with Grade 2 or greater reactogenicity (i.e., solicited adverse events) from Day 0 through Day 7 after administration of investigational medical product (IMP).
7 days
Safety - IP related unsolicited adverse events
Délai: 28 days
Proportion of volunteers with IP-related unsolicited adverse events (AEs), including safety laboratory (biochemical, hematological) parameters, from the day of IMP administration up to 28 days post administration
28 days
Safety - IMP related SAEs
Délai: 168 days
Proportion of volunteers with IP-related serious adverse events (SAEs) throughout the study period
168 days
Safety - pIMDs
Délai: 168 days
Proportion of volunteers with potential immune-mediated diseases (pIMDs) from the day of IMP administration throughout the study period
168 days

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Immunogenicity - Frequency of Ab responses
Délai: From enrollment to the end of study observation at Day 168
Frequency IgG Env binding and neutralizing antibody boosting after vaccination with BG505 SOSIP.GT1.1 gp140 vaccine in PWH on ART, with and without bnAb activity compared to pre-immunization baseline.
From enrollment to the end of study observation at Day 168
Immunogenicity - Magnitude Ab responses
Délai: 168 days
Magnitude of IgG Env binding and neutralizing antibody boosting after vaccination with BG505 SOSIP.GT1.1 gp140 vaccine in PWH on ART, with and without bnAb activity compared to pre-immunization baseline.
168 days

Collaborateurs et enquêteurs

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

Les enquêteurs

  • Directeur d'études: Huldrych Günthard, Prof. Dr. med., University of Zurich, Universitiy Hospital Zurich
  • Chaise d'étude: Alexandra Trkola, Prof. Dr., University of Zurich

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'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)

25 février 2025

Achèvement primaire (Estimé)

1 janvier 2028

Achèvement de l'étude (Estimé)

1 mars 2028

Dates d'inscription aux études

Première soumission

13 janvier 2025

Première soumission répondant aux critères de contrôle qualité

12 août 2026

Première publication (Réel)

18 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

11 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

10 septembre 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • SNCTP000006192 BASEC2024-01623

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

produit fabriqué et exporté des États-Unis.

Oui

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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