- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT00500058
A Phase I, Dose-Escalation Study to Assess the Safety and Biological Activity of Recombinant Human Interleukin-18
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"
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Tipo di studio
Iscrizione (Effettivo)
Fase
- Fase 1
Contatti e Sedi
Luoghi di studio
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Illinois
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Chicago, Illinois, Stati Uniti, 60637
- GSK Investigational Site
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Indiana
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Indianapolis, Indiana, Stati Uniti, 46202
- GSK Investigational Site
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
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Sperimentale: 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.
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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.
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Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
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safety/tolerability of combination treatment for 4 weeks safety/tolerability of SB-485232 for additional 8 weeks
Lasso di tempo: 12 weeks
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12 weeks
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Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
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assess blood values of combination treatment for 4 weeks assess blood values of SB-485232 for additional 8 weeks
Lasso di tempo: 12 weeks
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12 weeks
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Pharmacokinetic parameters for SB-485232 and Rituxan: AUCtau, Cmax, and Cmin.
Lasso di tempo: 12 weeks
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12 weeks
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Pharmacodynamic biomarker responses:
Lasso di tempo: 12 weeks
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12 weeks
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Plasma IFN-γ, GMCSF, IP-10, MIG, and MCP-1 changes
Lasso di tempo: from baseline and predose
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from baseline and predose
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Plasma IL-18BP change
Lasso di tempo: from baseline
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from baseline
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PBMC phenotype changes
Lasso di tempo: from baseline and pre-dose
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from baseline and pre-dose
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Activated NK cells (CD16+/CD56+/CD3-/CD69+/FasL+ or IL-18Ra+)
Lasso di tempo: 12 weeks
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12 weeks
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Activated cytolytic T cells (CD8+/CD4-/CD3+/CD69+ FasL+ or IL- 18Ra+)
Lasso di tempo: 12 weeks
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12 weeks
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Activated B cells (CD19+/CD25-/CD3-/CD69+)
Lasso di tempo: 12 weeks
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12 weeks
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Activated Neutrophils/Monocytes (CD11b+/CD16+/CD64+/CD14+/CD45+/CD69+)
Lasso di tempo: 12 weeks
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12 weeks
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Regulatory T-cells (FoxP3+/CD25+/CD4+/CD127+)
Lasso di tempo: 12 weeks
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12 weeks
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Immunogenicity (anti-SB-485232 and anti-Rituximab antibodies)
Lasso di tempo: 12 weeks
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12 weeks
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Anti-tumor activity (Radiographic tumor assessments)
Lasso di tempo: 12 weeks
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12 weeks
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CD16 (FcγRIIIA) 158V/F genotyping
Lasso di tempo: 12 weeks
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12 weeks
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Collaboratori e investigatori
Sponsor
Pubblicazioni e link utili
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Effettivo)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
- Malattie del sistema immunitario
- Neoplasie per tipo istologico
- Neoplasie
- Malattie linfoproliferative
- Malattie linfatiche
- Disturbi immunoproliferativi
- Linfoma
- Linfoma non Hodgkin
- Effetti fisiologici delle droghe
- Agenti antireumatici
- Agenti antineoplastici
- Fattori immunologici
- Agenti antineoplastici, immunologici
- Rituximab
Altri numeri di identificazione dello studio
- ILI105618
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Descrizione del piano IPD
Dati/documenti di studio
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Protocollo di studio
Identificatore informazioni: ILI105618Commenti informativi: For additional information about this study please refer to the GSK Clinical Study Register
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Modulo di segnalazione del caso annotato
Identificatore informazioni: ILI105618Commenti informativi: For additional information about this study please refer to the GSK Clinical Study Register
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Modulo di consenso informato
Identificatore informazioni: ILI105618Commenti informativi: For additional information about this study please refer to the GSK Clinical Study Register
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Piano di analisi statistica
Identificatore informazioni: ILI105618Commenti informativi: For additional information about this study please refer to the GSK Clinical Study Register
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Set di dati del singolo partecipante
Identificatore informazioni: ILI105618Commenti informativi: For additional information about this study please refer to the GSK Clinical Study Register
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Rapporto di studio clinico
Identificatore informazioni: ILI105618Commenti informativi: For additional information about this study please refer to the GSK Clinical Study Register
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Specifica del set di dati
Identificatore informazioni: ILI105618Commenti informativi: For additional information about this study please refer to the GSK Clinical Study Register
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Linfoma non Hodgkin
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Marker Therapeutics, Inc.ReclutamentoLinfoma di Hodgkin | Linfoma non Hodgkin | Linfoma di Hodgkin, adulto | Linfoma non Hodgkin, adulto | Linfoma non Hodgkin, refrattario | Linfoma non Hodgkin, recidivato | Linfoma di Hodgkin, recidivante, adultoStati Uniti
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National Cancer Institute (NCI)CompletatoLinfoma di Hodgkin dell'adulto ricorrente | Linfoma di Hodgkin adulto stadio III | Linfoma di Hodgkin adulto stadio IV | Linfoma di Hodgkin infantile ricorrente/refrattario | Linfoma di Hodgkin infantile in stadio III | Linfoma di Hodgkin infantile in stadio IV | Linfoma di Hodgkin adulto stadio I | Linfoma di Hodgkin infantile in stadio... e altre condizioniStati Uniti
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Tomsk National Research Medical Center of the Russian...Uppsala UniversityCompletatoLinfoma di Hodgkin, adulto | Linfoma non Hodgkin, adultoFederazione Russa
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Tessa TherapeuticsAttivo, non reclutanteLinfoma di Hodgkin, adulto | Malattia di Hodgkin ricorrente | Malattia di Hodgkin refrattaria | Malattia di Hodgkin, pediatricaStati Uniti
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Fred Hutchinson Cancer CenterNational Cancer Institute (NCI)TerminatoLinfoma di Hodgkin ricorrente | Linfoma di Hodgkin refrattario | Linfoma non Hodgkin a cellule B refrattario | Linfoma non Hodgkin a cellule T refrattario | Linfoma non Hodgkin ricorrente a cellule B | Linfoma non Hodgkin ricorrente a cellule TStati Uniti
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Academic and Community Cancer Research UnitedNational Cancer Institute (NCI)Attivo, non reclutanteLinfoma di Hodgkin in stadio III di Ann Arbor | Linfoma di Hodgkin in stadio IIIA di Ann Arbor | Linfoma di Hodgkin in stadio IIIB di Ann Arbor | Linfoma di Hodgkin stadio IV di Ann Arbor | Linfoma di Hodgkin allo stadio IVA di Ann Arbor | Linfoma di Hodgkin allo stadio IVB di Ann Arbor | Linfoma... e altre condizioniStati Uniti
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Rita AssiReclutamentoLinfoma a cellule B | Linfoma di Hodgkin refrattario | Linfoma non Hodgkin refrattario | Linfoma non Hodgkin recidivato | Linfoma di Hodgkin recidivatoStati Uniti
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University of WashingtonAttivo, non reclutanteLinfoma di Hodgkin ricorrente | Linfoma di Hodgkin refrattario | Linfoma non Hodgkin ricorrente | Linfoma non Hodgkin refrattarioStati Uniti
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CytokineticsCompletatoLinfoma non-Hodgkin | Morbo di HodgkinStati Uniti, Federazione Russa
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Fred Hutchinson Cancer CenterNational Cancer Institute (NCI)CompletatoLinfoma di Hodgkin ricorrente | Linfoma di Hodgkin refrattario | Linfoma Mantellare Ricorrente | Linfoma non Hodgkin a cellule B refrattario | Linfoma non Hodgkin a cellule T refrattario | Linfoma non Hodgkin ricorrente a cellule B | Linfoma non Hodgkin ricorrente a cellule T | Linfoma mantellare refrattarioStati Uniti
Prove cliniche su SB-485232
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GlaxoSmithKlineCompletatoAttività antitumorale di SB-485232 in pazienti con melanoma metastatico precedentemente non trattatoMelanomaAustralia, Stati Uniti
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GlaxoSmithKlineCompletatoCancro del tumore solidoStati Uniti
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GlaxoSmithKlineCompletatoLinfoma | Cancro del tumore solidoStati Uniti
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Michael John RobertsonNovartisCompletato
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GlaxoSmithKlineCompletatoNeoplasie, OvaricoStati Uniti
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Abramson Cancer Center of the University of PennsylvaniaRitiratoCancro ovarico, delle tube di Falloppio e del peritoneoStati Uniti
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University of MinnesotaCompletatoMalattia cardiovascolare | Diabete di tipo 2Stati Uniti
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Sangamo TherapeuticsAttivo, non reclutanteEmofilia B | Mucopolisaccaridosi I | Mucopolisaccaridosi IIStati Uniti
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Nguyen Thi Trieu, MDTran Minh DucCompletatoCirrosi del fegatoVietnam, Stati Uniti
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Medica Cor Heart HospitalSconosciutoStenosi coronarica dell'ostio | MionecrosiBulgaria