- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT05077137
Une étude de faisabilité utilisant le rappel immunitaire pour augmenter la réponse à la thérapie par points de contrôle (TdVax)
The purpose of this study is to determine the safety and feasibility of administering the Tetanus Diptheria Vaccine (Td) or Polio Boost Immunization (IPOL) to patients with metastatic melanoma who are receiving immune checkpoint inhibitor (IO) therapy per standard of care. Subjects will have the vaccine at cycle 4 of IO therapy and will have research blood and tissue samples collected prior to starting IO therapy, at cycle 4 prior to vaccine administration, and at 12-17 days post vaccine.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- La phase 1
Contacts et emplacements
Coordonnées de l'étude
- Nom: Carol Ann Wiggs, BSN
- Numéro de téléphone: 919-684-0281
- E-mail: carolann.wiggs@duke.edu
Lieux d'étude
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North Carolina
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Durham, North Carolina, États-Unis, 27710
- Recrutement
- Duke University Medical Center
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Contact:
- Carol Ann Wiggs, BSN
- Numéro de téléphone: 919-684-0281
- E-mail: carolann.wiggs@duke.edu
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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:
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Histologically confirmed advanced metastatic melanoma
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Male or female participants who are at least 18 years of age on the day of signing informed consent
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Participants must be planned or scheduled by their treating physician to receive PD-1 therapy or PD-1 plus anti CTLA-4 therapy as standard of care
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Participant (or legally acceptable representative if applicable) provides written informed consent for the trial
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Participant must have at least 1 lesion that is at least 8 mm in size and is cutaneous, subcutaneous, palpable, or amenable to ultrasound guided core biopsy. The lesion chosen for biopsy can also be a target lesion but does not have to be a target lesion
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Adequate organ function as defined below. Standard of care labs drawn within 45 days prior to consent may be used for the purposes of determining eligibility
- ANC >/= 1500/uL
- platelets >/=100,000/uL
- Hemoglobin >/= 9.0 g/dL
Exclusion Criteria:
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Uveal or mucosal melanoma
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Any women known to be pregnant or breastfeeding
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Any prior systemic therapy for metastatic melanoma (prior surgery is allowed)
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Known diagnosis of immunodeficiency or receiving chronic systemic steroid therapy (in doses exceeding 10 mg daily of prednisone or equivalent), or any other form of immunosuppressive therapy within 7 days prior to first research biopsy
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Patients with symptomatic CNS metastases and/or carcinomatous meningitis
a) Patients with asymptomatic, stable CNS metastases are allowed provided that they are not on >10mg prednisone daily
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History of or active (non-infectious) pneumonitis that required steroids
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Active infection requiring systemic therapy
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Known history of Human Immunodeficiency Virus (HIV) infection
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Known history of Hepatitis B (defined as Hepatitis B surface antigen [HBsAg] reactive) or known active Hepatitis C virus (defined as HCV RNA [qualitative] is detected) infection. NOTE: no testing for Hepatitis B or Hepatitis C is required
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Known history of active TB (Bacillus Tuberculosis)
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History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with subject's participation for the full duration of the study, or make it not in the best interest of the subject to participate, in the opinion of the treating physician
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Known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial
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History of allogenic tissue or solid organ transplant
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History of allergic reaction to IPOL or Td vaccine
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Receipt of Td vaccine within 30 days prior to starting IO therapy
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation séquentielle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Td Vaccine
The first 15 subjects enrolled will receive the Td (tetanus diphtheria) vaccine at cycle 4 of IO therapy. The Td vaccine is administered as 0.5 mL intramuscular injection in the extremity (thigh or upper arm) in closest proximity to the largest tumor. |
tetanus and diphtheria toxoids
Autres noms:
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Expérimental: IPOL Vaccine
Subjects 16 through 25 will receive the IPOL (polio booster) vaccine at cycle 4 of IO therapy. The IPOL vaccine is administered as 0.5 mL intramuscular or subcutaneous injection in the extremity (thigh or upper arm) in closest proximity to the largest tumor |
trivalent inactivated polio vaccine
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Number of subjects out of the proposed 25 that successfully receive the vaccine after 4 cycles of IO therapy
Délai: informed consent through date of vaccine (est apx 4-5 months)
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Evaluable patients are defined as those who receive four cycles of IO therapy and then receive a Td or IPOL vaccine |
informed consent through date of vaccine (est apx 4-5 months)
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Safety, as measured by the change in the number and severity of adverse events deemed related to the vaccine or study procedures (blood draw and biopsies)
Délai: Baseline, cycle 4 of IO therapy (apx 12-16 weeks), 12-17 days post vaccine, SOC scan following vaccine (apx 8-12 weeks post vaccine)
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Adverse events will only include those that are determined to be related to the study vaccine or study procedures (blood draw and biopsies) |
Baseline, cycle 4 of IO therapy (apx 12-16 weeks), 12-17 days post vaccine, SOC scan following vaccine (apx 8-12 weeks post vaccine)
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Preliminary efficacy, as measured by objective response rate
Délai: up to 36 months
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Number of patients that experience tumor response vs. stable disease vs. progression as determined by PI assessment of standard of care scans |
up to 36 months
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Georgia Beasley, MD, Duke University
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Tumeurs par site
- Tumeurs
- Tumeurs par type histologique
- Maladies de la peau
- Tumeurs neuroectodermiques
- Tumeurs, cellules germinales et embryonnaires
- Tumeurs, tissu nerveux
- Tumeurs neuroendocrines
- Nevi et mélanomes
- Tumeurs cutanées
- Maladies de la peau et du tissu conjonctif
- Mélanome
- Produits biologiques
- Mélanges complexes
- Vaccins bactériens
- Vaccins
- Diphtérie toxoïde
- Toxoïdes
- Tetanus toxoïde
- Vaccins, combinés
- Vaccin contre la diphtérienne-tétanique
Autres numéros d'identification d'étude
- Pro00108367
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
IPD will only be used internally by the study team
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
produit fabriqué et exporté des États-Unis.
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 .