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F901318 Multiple Ascending Dose Study

16. september 2016 oppdatert av: 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.

Studieoversikt

Status

Fullført

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Faktiske)

72

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • UK
      • London, UK, Storbritannia, NW10 7EW
        • Hammersmith Medicines Research

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 45 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Mann

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Trippel

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: A active
Six subjects receiving F901318 1.5 mg/kg intravenously for eight days
Administration of active compound
Placebo komparator: A placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administrering av placebo
Eksperimentell: B active
Six subjects receiving F901318 3 mg/kg intravenously for eight days
Administration of active compound
Placebo komparator: B placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administrering av placebo
Eksperimentell: C active
Six subjects receiving F901318 4 mg/kg intravenously for eight days
Administration of active compound
Placebo komparator: C placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administrering av placebo
Eksperimentell: D1 active
Six subjects dosed for one day with F901318 intravenously dose to be determined
Administration of active compound
Placebo komparator: D1 placebo
Two subjects receiving F901318 placebo intravenously for one day
Administrering av placebo
Eksperimentell: E1 active
Six subjects dosed for one day with F901318 intravenously dose to be determined
Administration of active compound
Placebo komparator: E1 placebo
Two subjects receiving F901318 placebo intravenously for one day
Administrering av placebo
Eksperimentell: F1 active
Six subjects dosed for one day with F901318 intravenously dose to be determined
Administration of active compound
Placebo komparator: F1 placebo
Two subjects receiving F901318 placebo intravenously for one day
Administrering av placebo
Eksperimentell: D2 active
Six subjects dosed for eight days with F901318 intravenously dose to be determined
Administration of active compound
Placebo komparator: D2 placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administrering av placebo
Eksperimentell: E2 active
Six subjects dosed for eight days with F901318 intravenously dose to be determined
Administration of active compound
Placebo komparator: E2 placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administrering av placebo
Eksperimentell: F2 active
Six subjects dosed for eight days with F901318 intravenously dose to be determined
Administration of active compound
Placebo komparator: F2 placebo
Two subjects receiving F901318 placebo intravenously for eight days
Administrering av placebo

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
safety: adverse events
Tidsramme: 13 days
adverse events
13 days

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
pharmacokinetics AUC
Tidsramme: 13 days
area under concentration time curve
13 days
pharmacokinetics Cmin
Tidsramme: 13 days
drug level in blood 24 hours after dosing
13 days

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

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

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. februar 2015

Primær fullføring (Faktiske)

1. september 2016

Studiet fullført (Faktiske)

1. september 2016

Datoer for studieregistrering

Først innsendt

15. januar 2015

Først innsendt som oppfylte QC-kriteriene

20. januar 2015

Først lagt ut (Anslag)

21. januar 2015

Oppdateringer av studieposter

Sist oppdatering lagt ut (Anslag)

19. september 2016

Siste oppdatering sendt inn som oppfylte QC-kriteriene

16. september 2016

Sist bekreftet

1. august 2016

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • F901318-01-02-14

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