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F901318 Multiple Ascending Dose Study

16 septembre 2016 mis à jour par: F2G Biotech GmbH

F901318 - A Phase I, Double-Blind, Placebo Controlled, Single and Multiple Ascending Intravenous Dose, Safety, Tolerability and Pharmacokinetic Study in Healthy Male Subjects

Double blind, placebo controlled, parallel group ascending dose study evaluating single and multiple (x8 days) dose levels of F901318 in groups of male healthy subjects with the objective of defining a dosing schedule for phase ll clinical trials. F901318, a novel and potent antifungal agent for the treatment of invasive aspergillosis, will be delivered intravenously in a range of dosing schedules driven by pharmacokinetic evaluation in real time. Safety and tolerability of those schedules will also be assessed.

Aperçu de l'étude

Statut

Complété

Les conditions

Description détaillée

Double blind, placebo controlled, ascending single and multiple intravenous dose, sequential group study. This will be a study in two parts. In the first part, up to twenty four subjects will complete the study in up to 3 cohorts (Groups A to C), each group consisting of 8 subjects, six of whom will receive active compound and two will receive placebo for eight days. Each subject will be on study for approximately 7 weeks. Each subject will participate in one treatment cohort only, residing at the Clinical Research Unit (CRU) from Day -1 (the day before dosing) to Day 13 (120 hours post the last dose).

This first part (Part 1) will test doses already evaluated in the previous single ascending dose study (F901318-01-01-14, 0.25-4 mg/kg given over 4 hours). The dose levels for the study are expected to be 1.5, 3 and 4 mg/kg/day given as a four hour infusion once daily.

In the second part of the study (Part 2), doses higher than those previously evaluated may be studied and/or different dosing schedules designed to deliver a maximum tolerated dose over 24 hours. If a dose level higher than those previously studied is chosen, there will be an optional single dose studied initially for safety and pharmacokinetic profile (Part 2A), followed about 14 days later in another group of subjects by exposure at that same dose level over 8 consecutive days (Part 2B). These higher doses may be given in a once or twice daily dosing schedule. Six subjects will receive active compound and two will receive placebo in both the single dose and multiple dose cohorts. The single dose cohorts will receive study drug in a sentinel group design in which two subjects receive study drug (one active and one placebo) on the first day and the rest of the group one day later. There will be a review of safety data by the Principal Investigator and the Medical Monitor after the first two subjects have been dosed and before the last six subjects are dosed in each cohort in part 2A.

In Part 2, up to forty-eight subjects will complete the study in up to 6 cohorts (Part 2A, Groups D1 to F1, single day dosing, and Part 2B, Groups D2 to F2 eight days' dosing). Subjects in Parts 1 and 2B will be on the study for approximately 7 weeks and Part 2A for approximately 8 weeks. Each subject will participate in one treatment cohort only, residing at the Clinical Research Unit (CRU) from Day -1 (the day before dosing) to Day 6 (120 hours after the single dose in Parts 1 and 2A) and from Day -1 (the day before dosing) to Day 13 (120 hours after the first dose in Part 2B). The proposed total daily dose levels for Part 2 will be up to 10 mg/kg/day given either once daily or in two split daily doses. The duration of the infusions will be between 2 and 24 hours which may include a loading dose to achieve therapeutic plasma concentrations as quickly as possible.

All subjects will return for a post-study visit 8 to 10 days after the last dose of study medication.

Type d'étude

Interventionnel

Inscription (Réel)

72

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

    • UK
      • London, UK, Royaume-Uni, NW10 7EW
        • Hammersmith Medicines Research

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 à 45 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Homme

La description

Inclusion Criteria:

  1. Subjects will be males of any ethnic origin between 18 and 45 years of age and weighing 60-100 kg inclusive
  2. Subjects must be in good health, as determined by a medical history, physical examination, 12-lead electrocardiogram (ECG) and clinical laboratory evaluations (congenital non haemolytic hyperbilirubinaemia is acceptable)
  3. Subjects will have given their written informed consent to participate in the study and to abide by the study restrictions
  4. Subjects must have ophthalmology assessments within the normal limits at screening. This includes normal Meibomian gland function

Exclusion Criteria:

  1. Male subjects who are not willing to use appropriate contraception (such as a condom) during the study and until follow up
  2. Subjects who have received any prescribed systemic or topical medication within 14 days of dosing with study drug unless in the opinion of the Investigator and the Medical Monitor the medication will not interfere with the study procedures or compromise safety
  3. Subjects who have used any non-prescribed systemic or topical medication (including herbal remedies) within 7 days of dosing with study drug (with the exception of vitamin/mineral supplements and paracetamol) unless in the opinion of the Investigator and the Medical Monitor the medication will not interfere with the study procedures or compromise safety
  4. Subjects who have received any medications, including St John's Wort, known to chronically alter drug absorption or elimination processes within 30 days of dosing with study drug unless in the opinion of the Investigator and the Medical Monitor the medication will not interfere with the study procedures or compromise safety
  5. Subjects who are still participating in a clinical study (e.g. attending follow-up visits) or who have participated in a clinical study involving administration of an investigational drug (new chemical or biological entity) in the past 3 months since the last dose.

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: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Tripler

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: A active
Six subjects receiving F901318 1.5 mg/kg intravenously for eight days
Administration of active compound
Comparateur placebo: A placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administration de placebo
Expérimental: B active
Six subjects receiving F901318 3 mg/kg intravenously for eight days
Administration of active compound
Comparateur placebo: B placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administration de placebo
Expérimental: C active
Six subjects receiving F901318 4 mg/kg intravenously for eight days
Administration of active compound
Comparateur placebo: C placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administration de placebo
Expérimental: D1 active
Six subjects dosed for one day with F901318 intravenously dose to be determined
Administration of active compound
Comparateur placebo: D1 placebo
Two subjects receiving F901318 placebo intravenously for one day
Administration de placebo
Expérimental: E1 active
Six subjects dosed for one day with F901318 intravenously dose to be determined
Administration of active compound
Comparateur placebo: E1 placebo
Two subjects receiving F901318 placebo intravenously for one day
Administration de placebo
Expérimental: F1 active
Six subjects dosed for one day with F901318 intravenously dose to be determined
Administration of active compound
Comparateur placebo: F1 placebo
Two subjects receiving F901318 placebo intravenously for one day
Administration de placebo
Expérimental: D2 active
Six subjects dosed for eight days with F901318 intravenously dose to be determined
Administration of active compound
Comparateur placebo: D2 placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administration de placebo
Expérimental: E2 active
Six subjects dosed for eight days with F901318 intravenously dose to be determined
Administration of active compound
Comparateur placebo: E2 placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administration de placebo
Expérimental: F2 active
Six subjects dosed for eight days with F901318 intravenously dose to be determined
Administration of active compound
Comparateur placebo: F2 placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administration de placebo

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
safety: adverse events
Délai: 13 days
adverse events
13 days

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
pharmacokinetics AUC
Délai: 13 days
area under concentration time curve
13 days
pharmacokinetics Cmin
Délai: 13 days
drug level in blood 24 hours after dosing
13 days

Collaborateurs et enquêteurs

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

Parrainer

Les enquêteurs

  • Chercheur principal: Frans van den Berg, MB ChB, Hammersmith Medicines Research

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

1 février 2015

Achèvement primaire (Réel)

1 septembre 2016

Achèvement de l'étude (Réel)

1 septembre 2016

Dates d'inscription aux études

Première soumission

15 janvier 2015

Première soumission répondant aux critères de contrôle qualité

20 janvier 2015

Première publication (Estimation)

21 janvier 2015

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

19 septembre 2016

Dernière mise à jour soumise répondant aux critères de contrôle qualité

16 septembre 2016

Dernière vérification

1 août 2016

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • F901318-01-02-14

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 .

Essais cliniques sur Aspergillose invasive

Essais cliniques sur Placebo

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