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A Phase I, Dose-Escalation Study to Assess the Safety and Biological Activity of Recombinant Human Interleukin-18

24 juillet 2017 mis à jour par: GlaxoSmithKline

A Phase I, Dose-Escalation Study to Assess the Safety and Biological Activity of Recombinant Human Interleukin-18 (SB-485232) Administered by Intravenous Infusion in Combinationwith Rituximab in Adult Patients With B Cell Non-Hodgkin'sLymphoma"

The purpose is to identify a dose of SB-485232 which is safe, tolerable and effective when used in combination with Rituximab in patients with non-Hodgkin's lymphoma (NHL). This study will use a standard treatment regimen of Rituximab in combination with rising doses of SB-485232. The dose selected from this study will be used in a future studies.

Aperçu de l'étude

Statut

Complété

Les conditions

Type d'étude

Interventionnel

Inscription (Réel)

24

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

    • Illinois
      • Chicago, Illinois, États-Unis, 60637
        • GSK Investigational Site
    • Indiana
      • Indianapolis, Indiana, États-Unis, 46202
        • GSK Investigational Site

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

18 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Histologically confirmed diagnosis of any subtype of CD20+ B cell NHL. Subjects must have disease that progressed after standard therapy or for which there is no effective standard therapy (including high-dose therapy and autologous stem cell transplantation). NOTE: If the subject has had a prior autologous stem cell transplant, it must have occurred at least three months prior to screening and the subject must be fully recovered from any acute toxicities.
  • Prior treatment with Rituximab is allowed, provided it was completed at least six months before study enrollment.
  • Male or female ≥ 18 years of age.
  • Measurable or evaluable disease.
  • Predicted life expectancy of at least 12 weeks.
  • ECOG Performance Status of 0 or 1.
  • No chemotherapy, immunotherapy, hormonal therapy, or biological therapy for cancer, radiotherapy, or surgical procedures (except for minor surgical procedures) within four weeks before beginning treatment with SB-485232 (6 weeks for nitrosoureas and mitomycin C). Subjects must have recovered from toxicities (incurred as a result of previous therapy) sufficiently to be entered into a Phase I study.
  • A signed and dated written informed consent form is obtained from the subject.
  • The subject is able to understand and comply with protocol requirements, timetables, instructions and protocol-stated restrictions.

The subject is likely to maintain good venous blood access for PK and PD sampling throughout the study.

  • A female is eligible to enter and participate in the study if she is of:

    a. non-childbearing potential (i.e., physiologically incapable of becoming pregnant) including any female who:

  • has had a hysterectomy,
  • has had a bilateral oophorectomy (ovariectomy),
  • has had a bilateral tubal ligation,
  • is post-menopausal (demonstrate total cessation of menses for greater than 1year), If amenorrheic for less than one year, post-menopausal status will be confirmed by serum follicle stimulating hormone (FSH) and oestradiol concentrations at screening. or, b. childbearing potential, has a negative serum pregnancy test at the Screen Visit, and agrees to one of the following GSK acceptable contraceptive methods:
  • any intrauterine device (IUD) with a documented failure rate of less than

    1% per year.

  • vasectomized partner who is sterile prior to the female subject's entry and is the sole sexual partner for that female.
  • oral contraceptive (either combined or progesterone only).
  • because of the unacceptable failure rate of barrier (chemical and/or physical) methods, the barrier method of contraception must only be used in combination with other acceptable methods described above.
  • Adequate organ function,

Exclusion Criteria:

  • Women who are pregnant or are breast-feeding.
  • Significant cardiac, pulmonary, metabolic, renal, hepatic, gastrointestinal or autoimmune conditions that in the opinion of the investigator and/or GSK medical monitor, places the subject at an unacceptable risk as participant in this trial.
  • The subject has diabetes mellitus with poor glycemic control.
  • The subject has a history of human immunodeficiency virus (HIV) or other immunodeficiency disease.
  • The subject has positive Hepatitis B surface antigen.
  • Corrected QT interval (QTc) > 480msec.
  • The subject has a history of a severe infusion related reaction or tumor lysis syndrome following treatment with Rituximab (Section 10.2.2).
  • The subject has a circulating malignant cell count > 25,000/mm3 in peripheral blood.
  • The subject has known anaphylaxis or IgE-mediated hypersensitivity to murine proteins.
  • The subject has an acute infection or severe or uncontrolled infections requiring systemic antibiotic therapy.
  • Any serious medical or psychiatric disorder that would interfere with subject safety or informed consent.
  • Known leptomeningeal disease or evidence of prior or current metastatic brain disease. Routine screening with central nervous system (CNS) imaging studies (CT or MRI) is required only if clinically indicated.
  • Receiving concurrent chemotherapy, immunotherapy, radiotherapy, or investigational therapy.
  • Oral corticosteroids within 14 days of study entry.
  • History of alcohol abuse within six months of screening or alcohol consumption in the past six months exceeding seven drinks/week for women and 14 drinks/week for men (where 1 drink = 5 ounces of wine or 12 ounces of beer or 1.5 ounces of hard liquor).
  • History of ventricular arrhythmias requiring drug or device therapy.
  • Any unresolved or unstable serious toxicity from prior administration of another investigational drug.
  • Any investigational drug within 30 days or five half-lives (whichever is longer) preceding the first dose of SB-485232.
  • Donation of blood in excess of 500 mL within a 56-day period prior to dosing.

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: Traitement
  • Répartition: Non randomisé
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: SB-485232+Rituximab
Rituximab 375 milligrams per square meter (mg/m^2) will be administered to subjects with CD20+ B cell lymphoma by intravenous (IV) infusion once a week for four consecutive weeks on Day 1 of Weeks 1 to 4. SB-485232 will be administered by IV infusion over a 2 hour period, at doses ranging from 1 microgram (μg)/kilogram (kg) to 100 μg/kg. SB-485232 will be given once a week for 12 consecutive weeks on Day 2 of Weeks 1 to 4 and Day 2 (± 1 day) of Weeks 5 to 12. SB-485232 will be infused at least 24 hours after the Rituximab infusion was started.
SB-485232 for injection, 7 mg/vial, will be available as a lyophilized cake. It will be reconstituted with 1.4 mL of water for injection. Each vial of this drug product is a clear, colorless solution containing 5 mg/mL of SB-485232.
Rituximab 375 mg/m^2 will be administered by IV infusion.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Délai
safety/tolerability of combination treatment for 4 weeks safety/tolerability of SB-485232 for additional 8 weeks
Délai: 12 weeks
12 weeks

Mesures de résultats secondaires

Mesure des résultats
Délai
assess blood values of combination treatment for 4 weeks assess blood values of SB-485232 for additional 8 weeks
Délai: 12 weeks
12 weeks
Pharmacokinetic parameters for SB-485232 and Rituxan: AUCtau, Cmax, and Cmin.
Délai: 12 weeks
12 weeks
Pharmacodynamic biomarker responses:
Délai: 12 weeks
12 weeks
Plasma IFN-γ, GMCSF, IP-10, MIG, and MCP-1 changes
Délai: from baseline and predose
from baseline and predose
Plasma IL-18BP change
Délai: from baseline
from baseline
PBMC phenotype changes
Délai: from baseline and pre-dose
from baseline and pre-dose
Activated NK cells (CD16+/CD56+/CD3-/CD69+/FasL+ or IL-18Ra+)
Délai: 12 weeks
12 weeks
Activated cytolytic T cells (CD8+/CD4-/CD3+/CD69+ FasL+ or IL- 18Ra+)
Délai: 12 weeks
12 weeks
Activated B cells (CD19+/CD25-/CD3-/CD69+)
Délai: 12 weeks
12 weeks
Activated Neutrophils/Monocytes (CD11b+/CD16+/CD64+/CD14+/CD45+/CD69+)
Délai: 12 weeks
12 weeks
Regulatory T-cells (FoxP3+/CD25+/CD4+/CD127+)
Délai: 12 weeks
12 weeks
Immunogenicity (anti-SB-485232 and anti-Rituximab antibodies)
Délai: 12 weeks
12 weeks
Anti-tumor activity (Radiographic tumor assessments)
Délai: 12 weeks
12 weeks
CD16 (FcγRIIIA) 158V/F genotyping
Délai: 12 weeks
12 weeks

Collaborateurs et enquêteurs

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

Parrainer

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)

31 juillet 2007

Achèvement primaire (Réel)

4 mars 2010

Achèvement de l'étude (Réel)

4 mars 2010

Dates d'inscription aux études

Première soumission

10 juillet 2007

Première soumission répondant aux critères de contrôle qualité

10 juillet 2007

Première publication (Estimation)

12 juillet 2007

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

26 juillet 2017

Dernière mise à jour soumise répondant aux critères de contrôle qualité

24 juillet 2017

Dernière vérification

1 juillet 2017

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) ?

OUI

Description du régime IPD

Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.

Données/documents d'étude

  1. Protocole d'étude
    Identifiant des informations: ILI105618
    Commentaires d'informations: For additional information about this study please refer to the GSK Clinical Study Register
  2. Formulaire de rapport de cas annoté
    Identifiant des informations: ILI105618
    Commentaires d'informations: For additional information about this study please refer to the GSK Clinical Study Register
  3. Formulaire de consentement éclairé
    Identifiant des informations: ILI105618
    Commentaires d'informations: For additional information about this study please refer to the GSK Clinical Study Register
  4. Plan d'analyse statistique
    Identifiant des informations: ILI105618
    Commentaires d'informations: For additional information about this study please refer to the GSK Clinical Study Register
  5. Ensemble de données de participant individuel
    Identifiant des informations: ILI105618
    Commentaires d'informations: For additional information about this study please refer to the GSK Clinical Study Register
  6. Rapport d'étude clinique
    Identifiant des informations: ILI105618
    Commentaires d'informations: For additional information about this study please refer to the GSK Clinical Study Register
  7. Spécification du jeu de données
    Identifiant des informations: ILI105618
    Commentaires d'informations: For additional information about this study please refer to the GSK Clinical Study Register

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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