- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT01258816
The Pharmacokinetics and Cardiac Properties of Elacytarabine (CP-4055)
A Phase I Study of the Human Pharmacokinetics and Cardiac Safety of Elacytarabine
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Elacytarabine is an investigational drug which is not commercially available. It consists of a fatty acid that is connected to cytarabine which is commonly used in treatment of AML. Due to the connection to a fatty acid, elacytarabine might have an increased uptake in blast cells and thereby increased efficacy.
The characterisation of the pharmacokinetics of an investigational drug, as well as the cardiac safety are essential. The PK of both elacytarabine and its metabolites will be assessed at defined timepoints before, during and after infusion. The cardiac safety of elacytarabine will be evaluated by triplicate ECG recordings at the same time points as the PK assessments.
Elacytarabine will be given as a continuous infusion for 5 days. The patients may continue with further courses of elacytarabine as long as the patient benefits from treatment with elacytarabine.
Type d'étude
Inscription (Réel)
Phase
- La phase 1
Contacts et emplacements
Lieux d'étude
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Barcelona, Espagne, 08035
- Hospital General de la Vall d' Hebron
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Cáceres, Espagne, 10003
- Hospital San Pedro Alcántara
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Catalunya
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Barcelona, Catalunya, Espagne, 08907
- ICO - Hospital Duran i Reynals
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Brighton, Royaume-Uni, BN2 5BE
- Brighton & Sussex University Hospitals NHS Trust
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Cardiff, Royaume-Uni, CF14 4XW
- University Hospital of Wales, Cardiff
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London, Royaume-Uni, EC1A 7BE
- St Bartholomew's Hospital
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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:
- Patients must have relapsed / refractory AML according to WHO classification (excluding acute promyelocytic leukaemia)
- Patients must have ECOG Performance Status (PS) of 0 - 2
- Patients must be 18 years of age or older
- Women of child-bearing potential must have a negative serum or urine pregnancy test within two weeks prior to treatment start
- Male and female fertile patients must use adequate contraception for the duration of the study, and males also for 3 months after the last elacytarabine dose
- Patients must be capable of understanding and complying with protocol requirements, and they must be able and willing to sign a written informed consent
Exclusion Criteria:
- A history of allergic reactions to egg. A history of CTCAE grade 3 or 4 allergic reactions to ara-C of
- A history of cancer that according to the investigator might confound the assessment of the endpoints of the clinical study
- Known positive status for human immunodeficiency virus (HIV)
- Pregnant and nursing patients
- Uncontrolled inter-current illness including, but not limited to, uncontrolled infection, or psychiatric illness/social situations that will limit compliance with study requirements
- Impairment of hepatic or renal function to such an extent that the patient, in the opinion of the investigator, will be exposed to an excessive risk if entered into the clinical study
- Active heart disease including myocardial infarction within previous 3 months, symptomatic coronary artery disease, arrhythmias not controlled by medications, or uncontrolled congestive heart failure. Any NYHA grade 3 or 4
- A history of familial long QT syndrome
- Patients with history of serious ventricular arrhythmia (VT or VT)
- ECG criteria at the eligibility visit: QTc ≥ 480 msec calculated using Fridericia's correction (QTcF = QT/RRO,33) or bradycardia (<50bpm) or criteria for left ventricular hypertrophy
- treatment with any medications known to produce QT prolongations
- Treatment with hydroxyurea or 6-mercaptopurine within the last 12 hours prior to treatment on this protocol or any other investigational or standard cytotoxic treatment within the last 14 days
9. Any medical condition which in the opinion of the investigator places the patient at an unacceptably high risk for toxicities
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
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Characterise the pharmacokinetics of elacytarabine in patients with relapsed/refractory Acute Myeloid Leukaemia
Délai: During first week of treatment course
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Collection of pheripheral blood samples at specified time points during first week of the treatment course for PK analyses
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During first week of treatment course
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
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Investigate the activity of elacytarabine measured as remission rate (CR + CRi)
Délai: After each course
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Bone marrow and/or blood examination
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After each course
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Number of patients with Adverse Events as a measure of safety and tolerability
Délai: Continuously during study
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Continuously during study
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Evaluate the cardiac safety of elacytarabine with focus on the QT/QTc intervals
Délai: During the first week of treatment
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Triplicate 12-lead ECG assessments will be done at specified time points before, during and after infusion
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During the first week of treatment
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Steven Knapper, MD, Cardiff University
Publications et 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
Autres numéros d'identification d'étude
- CP4055-109
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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