- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT01130376
Novel Interventions in HIV-1 Infection (IMIRC1003)
A Randomised, Open Labelled, Phase I, Safety, Toxicity, and Exploratory Immunogenicity Evaluation of Therapeutic Immunisation +/- IL-2, GM-CSF and Growth Hormone in HIV-1 Infected Subjects Receiving Highly Active Anti-retroviral Therapy
For several years there has been interest in why some people with HIV-1 progress more slowly to disease and have longer survival without Highly Active Antiretroviral Therapy (HAART) than others. The investigators and others have identified a few HIV positive individuals who can control their viral load for many years without HAART, these rare individuals do not lose their HIV-1-specific cellular immune responses, which are very important for controlling viral load. This group is referred to as long-term non-progressors (LTNP). Unlike LTNP the majority of HIV-1 infected individuals are chronic progressors (CP) who do not make effective HIV-1-specific cellular immune responses, even when on HAART. We propose to use a novel DNA vaccine boosted with immune based therapy (cytokines and hormones) to try to regenerate the missing HIV-1-specific cellular immune responses to make chronically infected HIV-1+ persons more like LTNP.
By injecting this novel DNA vaccine and immune based therapy into the people who are already infected with HIV-1, the immune system may be stimulated to mount a greater immune response not only to the vaccines but also to real HIV-1 particles and HIV-1-infected cells.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
This will be a randomised, Phase I, open label comparative study running for 52 weeks (2 screen visits 2 weeks apart followed by 48 weeks of study). 50 patients will be screened in the initial phase of which 30 clade B infected individuals will be randomised into the study, which will consist of 3 arms:
Arm 1 will ascertain vaccine safety and toxicity in the presence of cytokine/hormone therapy.
Arm 2 will identify vaccine safety and toxicity.
Arm 3 will indicate safety and toxicity of cytokine/hormone therapy.
The target patients are chronically HIV-1 clade B infected persons who will have had a nadir CD4 T-cell count of >200 cells/ul blood before they started ART. The current CD4 T-cell count should be >400 cells/ul blood. Patients may have received ART for any length of time, but currently should be receiving NNRTI or boosted-PI based HAART, and have a viral load below the level of detection (50 copies/ml plasma). Patients will be bled on two occasions before commencing IBT regimens, in order to establish baselines, and then at regular intervals thereafter (weeks 0,1,2,4,6,8,12,16,24 and 48).
The treatment regimens are consistent with previous findings in animal models which suggest that administration of IL-2 during the antigen-specific T-cell contraction phase of an immune response (between 8 and 15 days post-vaccination) may preserve and lengthen clinically relevant responses. Furthermore studies in man have demonstrated that IL-2 administered before immunisation in ART-treated HIV-1-infected patients does not increase specific lymphoproliferation of T cells.
Recent preliminary studies in HIV-1-infected individuals using tetanus vaccines the investigators have shown that IL-2 administered after immunisation may be more effective at inducing sustained tetanus-specific responses than IL-2 administered before immunisation or together with immunisation. The dosages used in this study are based on those used in previous pilot studies of the administration of IL-2 + GM-CSF and rhGH and at these levels the drugs have been shown to have both positive effect on the immune response and demonstrated clinical benefit whilst being at a level which is safe and well tolerated in HIV-1 positive individuals. The dosage of the vaccine was based on a previous study where a dosage of this level has been shown to induce an immune response although this response was transient. In summary the investigators aim to increase the survival of vaccine responses through the administration of cytokines/hormones and boost memory responses with further rounds of immunisation.
Type d'étude
Inscription (Réel)
Phase
- La phase 1
Contacts et emplacements
Lieux d'étude
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London, Royaume-Uni, SW10 9NH
- St. Stephen's AIDS Trust
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Documented HIV-1 positive result.
- Stable on HAART.
- Two screening viral loads of <50 cps/ml on 2 consecutive occasions at least one month apart.
- CD4 T cell count of >400 cells/ul.
- Nadir CD4 T cell count of >200 cells/ul.
- Over 18 years of age.
- Willing and able to provide informed consent.
- Female subjects must not be pregnant or lactating.
- Subjects must be using adequate double barrier method of contraception as appropriate.
Exclusion Criteria:
- Prior therapeutic vaccination.
- Acute illness within 2 weeks of the start of the study.
- Prior immunomodulatory therapy (e.g. IL-2, rhGH, GCSF, GM-CSF, HU)
- Receiving immunosuppressive medication (e.g. Steroids)
- Participation in other vaccine trials currently
- Patients with diabetes mellitus type 2
- Patients with cardiac abnormalities
- Patients with pre-existing autoimmune disease
- Patients with active neoplasia
- Patients with evidence of any progression or recurrence of an underlying intra-cranial lesion
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Vaccine and cytokines
Day 0: Patients receive GTU-MultiHIV B clade vaccine 1mg/ml administered as 10 intradermal injections of 100 µl/injection. Day 7-11: One week following this, patients receive a 5 day course of Cytokines: Aldesleukin (IL-2) Novartis UK (BD; 8 hours apart) 5 million units administered by SC injection. Sargramostim (GM-CSF) - Leukine™, Berlex Seattle US 150ug SC once daily 4 hours from rhIL-2 injections. Day 14-18: The following week, patients rhGH (Saizen™, Serono International, Geneva, Switzerland) 4mg/day self-administered SC. Further vaccine boosters are given on day 42 and day 84. GTU-MultiHIV B clade vaccine 1mg/ml being administered as 10 intradermal injections of 100 µl/injection. |
Dose given is 1mg/ml administered as 10 intradermal injections of 100 µl/injection distributed as 5 intradermal injections /left and right arm
5 Million Units administered twice daily for 5 days by subcutaneous injection on days 7, 8, 9, 10, and 11 after first vaccination. .
Autres noms:
150 ug administered subcutaneously once daily 4 hours from IL-2 injections
Autres noms:
4mg/day will be self administered by Subcutaneous injection for 5 days on days 14, 15, 16, 17 and 18 following first vaccination
Autres noms:
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Comparateur actif: Vaccine alone
Day 0: Patients are given GTU-MultiHIV B clade vaccine 1mg/ml administered as 10 intradermal injections of 100 µl/injections. Day 42: GTU-MultiHIV B clade vaccine as day 0. Day 84: GTU-MultiHIV B clade vaccine as day 0. |
Dose given is 1mg/ml administered as 10 intradermal injections of 100 µl/injection distributed as 5 intradermal injections /left and right arm
|
|
Comparateur actif: Cytokines alone
Day 7-11: One week following this, patients receive a 5 day course of Cytokines: Aldesleukin (IL-2) Novartis UK (BD; 8 hours apart) 5 million units administered by SC injection. Sargramostim (GM-CSF) - Leukine™, Berlex Seattle US 150ug SC once daily 4 hours from rhIL-2 injections. Day 14-18: The following week, patients rhGH (Saizen™, Serono International, Geneva, Switzerland) 4mg/day self-administered SC. |
5 Million Units administered twice daily for 5 days by subcutaneous injection on days 7, 8, 9, 10, and 11 after first vaccination. .
Autres noms:
150 ug administered subcutaneously once daily 4 hours from IL-2 injections
Autres noms:
4mg/day will be self administered by Subcutaneous injection for 5 days on days 14, 15, 16, 17 and 18 following first vaccination
Autres noms:
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
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The primary outcome will be analysis of safety and toxicity data in relation to grade 3 or above laboratory or clinical serious adverse event (SAE) which can be attributed to the treatments given
Délai: Weekly
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Weekly
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Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
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The secondary immunological outcomes will be percentage change from baseline to study time point in defined cellular immune responses.
Délai: weekly
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weekly
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Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Nesrina Imami, MD/PhD, Imperial College London
Publications et liens utiles
Liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Infections
- Effets physiologiques des médicaments
- Agents anti-infectieux
- Agents du système nerveux périphérique
- Agents antiviraux
- Agents anti-VIH
- Agents antirétroviraux
- Analgésiques
- Agents du système sensoriel
- Analgésiques, non narcotiques
- Agents antinéoplasiques
- Facteurs immunologiques
- Hormones, substituts hormonaux et antagonistes hormonaux
- Aldesleukine
- Les hormones
- Sargramostim
- Interleukine-2
Autres numéros d'identification d'étude
- CRO930
- G0501957 (Autre subvention/numéro de financement: Medical Research Council UK)
- 2008-000575024 (Identificateur de registre: EudraCT)
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