CClinicalTrials.gg
CompletedNCT02342574Updated Sep 19, 2016

F901318 Multiple Ascending Dose Study

A Phase 1 interventional study of F901318 and Placebo in Invasive Aspergillosis, sponsored by F2G Biotech GmbH. Completed at 1 site in United Kingdom. Open to male participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-09-19.

Sponsored by F2G Biotech GmbH · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
72
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Male
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Invasive Aspergillosis

Browse trials for

03

In context

Aspergillosis

201 studies on the registry are indexed under Aspergillosis; 22 are open to participants now.

This study's enrollment of 72 is above the median of 50 across 106 interventional studies indexed under Aspergillosis.

Browse Aspergillosis studies →

Lead sponsor

F2G Biotech GmbH is the lead sponsor of 20 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Male
Accepts healthy volunteers
Yes

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

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.
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
72 participants (actual)

Study arms

  • Experimental
    A active

    Six subjects receiving F901318 1.5 mg/kg intravenously for eight days

    Drug: F901318

  • Placebo comparator
    A placebo

    Two subjects receiving F901318 placebo intravenously for eight days

    Drug: Placebo

  • Experimental
    B active

    Six subjects receiving F901318 3 mg/kg intravenously for eight days

    Drug: F901318

  • Placebo comparator
    B placebo

    Two subjects receiving F901318 placebo intravenously for eight days

    Drug: Placebo

  • Experimental
    C active

    Six subjects receiving F901318 4 mg/kg intravenously for eight days

    Drug: F901318

  • Placebo comparator
    C placebo

    Two subjects receiving F901318 placebo intravenously for eight days

    Drug: Placebo

  • Experimental
    D1 active

    Six subjects dosed for one day with F901318 intravenously dose to be determined

    Drug: F901318

  • Placebo comparator
    D1 placebo

    Two subjects receiving F901318 placebo intravenously for one day

    Drug: Placebo

  • Experimental
    E1 active

    Six subjects dosed for one day with F901318 intravenously dose to be determined

    Drug: F901318

  • Placebo comparator
    E1 placebo

    Two subjects receiving F901318 placebo intravenously for one day

    Drug: Placebo

  • Experimental
    F1 active

    Six subjects dosed for one day with F901318 intravenously dose to be determined

    Drug: F901318

  • Placebo comparator
    F1 placebo

    Two subjects receiving F901318 placebo intravenously for one day

    Drug: Placebo

  • Experimental
    D2 active

    Six subjects dosed for eight days with F901318 intravenously dose to be determined

    Drug: F901318

  • Placebo comparator
    D2 placebo

    Two subjects receiving F901318 placebo intravenously for eight days

    Drug: Placebo

  • Experimental
    E2 active

    Six subjects dosed for eight days with F901318 intravenously dose to be determined

    Drug: F901318

  • Placebo comparator
    E2 placebo

    Two subjects receiving F901318 placebo intravenously for eight days

    Drug: Placebo

  • Experimental
    F2 active

    Six subjects dosed for eight days with F901318 intravenously dose to be determined

    Drug: F901318

  • Placebo comparator
    F2 placebo

    Two subjects receiving F901318 placebo intravenously for eight days

    Drug: Placebo

Interventions

  • DrugF901318

    Administration of active compound

  • DrugPlacebo

    Administration of placebo

06

What researchers measure

Primary outcomes

  1. safety: adverse events

    adverse events

    Time frame: 13 days

Secondary outcomes

  1. pharmacokinetics AUC

    area under concentration time curve

    Time frame: 13 days

  2. pharmacokinetics Cmin

    drug level in blood 24 hours after dosing

    Time frame: 13 days

07

Study locations

1 site
  • Hammersmith Medicines Research
    London, UK NW10 7EW, United Kingdom
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 19, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02342574
Lead sponsor
F2G Biotech GmbH
Collaborators
Hammersmith Medicines Research
Responsible party
Sponsor
First posted
Jan 21, 2015
Start date
Feb 2015
Primary completion
Sep 2016
Completion
Sep 2016
Last update
Sep 19, 2016

Study contacts

Frans van den Berg, MB ChB
principal investigator · Hammersmith Medicines Research

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion