Working...
ClinicalTrials.gov
ClinicalTrials.gov Menu
Trial record 9 of 51 for:    "Invasive Aspergillosis" | "Anti-Infective Agents"

Single Ascending Oral Dose Study of F901318

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT02394483
Recruitment Status : Completed
First Posted : March 20, 2015
Last Update Posted : September 19, 2016
Sponsor:
Collaborator:
Simbec-Orion Research
Information provided by (Responsible Party):
F2G Ltd.

Brief Summary:

Double blind, placebo controlled, ascending single oral dose, sequential group study. Forty subjects will complete the study in 5 cohorts (Groups A to E), each group consisting of 8 subjects. Each subject will be on study for approximately 6 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 post-dose). Each cohort will be dosed in a leading edge design in which two subjects will receive study drug (1 active and 1 placebo) on the first dosing day, and the last 6 will receive study drug (5 active and 1 placebo) on the second dosing day.

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

Cohorts will be dosed at 2 weekly intervals. There will be a review of safety data, after the first two subjects have been dosed and before dosing of the subsequent six subjects. There will be a complete review of safety and pharmacokinetic data of each cohort prior to each dose escalation.


Condition or disease Intervention/treatment Phase
Invasive Aspergillosis Drug: F901318 safety Drug: F901318 tolerability Drug: F901318 pharmacokinetics Other: Placebo safety Other: Placebo tolerability Other: Placebo pharmacokinetics Phase 1

  Hide Detailed Description

Detailed Description:

Male healthy subjects conforming to the selection criteria will be invited to take part in the study.

Screening visit (Visit 1) After giving fully informed, written consent, subjects will attend the clinic.

Subjects will undergo screening within 28 days prior to the first dose administration. Prior to the screening visit, subjects will:

  • Refrain from vigorous exercise for 7 days
  • Abstain from alcohol for 48 hours
  • Subjects will sign the consent form in the presence of a CRU physician prior to any screening procedures being performed. The information recorded for all subjects, regardless of their suitability for the study, will be retained and archived

The following information and procedures will be recorded and performed as part of the screening assessments:

  • Medical history
  • Ethnic origin, sex, age, height, weight, and BMI
  • Vital signs: supine blood pressure, supine pulse rate, and oral body temperature
  • Resting 12 lead ECG
  • Physical examination
  • Urine drugs of abuse screen, cotinine and breath alcohol
  • Fasting clinical laboratory and serology investigations

Up to 28 days after screening, subjects will attend the clinic. Subjects will be admitted to the research unit at approximately 13:00 hours in the afternoon the day before dosing (Day -1; -19 hours pre-dose). Urine will be subjected to a screen for drugs of abuse and there will be a breath test for alcohol and cotinine. Detection of any of these substances will disqualify the subject from the study. A physical examination, check of inclusion/exclusion criteria, clinical laboratory evaluations, oral temperature and body weight will be performed. Subjects will be asked whether they have experienced any adverse events or taken any concomitant medication since their previous visit. Supper will be served starting at 19.30 hours and a snack at 21.00 hours, following which subjects will be fasting. Water will be allowed ad libitum throughout.

On day 1, the total first urine void of the morning for each subject will be collected into a polyethylene container and, from this, a sample will be taken for urinalysis and pre-dose / baseline F901318 concentration. Within one hour before dosing commences (-1 hour), blood will be drawn for laboratory safety assessments (haematology and clinical chemistry), and pre-dose baseline F901318 and metabolites concentration. Supine and standing blood pressure and pulse rate in triplicate, body temperature and a 12-lead ECG will be recorded. The subjects will also be connected to continuous ECG recording from -1 hour until 12 hours after the start of dosing.

Subjects will be asked whether they have experienced any adverse events overnight. Any concomitant medications will be recorded.

Option 1: Subjects will then be dosed. This will be oral ingestion of a liquid formulation followed by 250 mL of water. Subjects will be dosed with regular (at least 5 minute) intervals between each subject.

After initial dosing, the following measurements and observations will be obtained:

• Blood samples for analysis of F901318 plasma concentration will be drawn at 15, 30, 45, 60, 75, 90, 120 minutes, then 3, 4, 6, 8, 10, 12, 18, 24, 36, 48, 72, 96 and 120 hours following dosing. Pharmacokinetic blood samples will be analysed and reviewed before each dose escalation. After the first dose administration, the timing of each blood sample may if necessary be adjusted within the 120-hour period for the subsequent dose escalation. The basis for this decision will depend upon the pharmacokinetic profiles obtained from the preceding group of subjects. All changes will be documented in a file note. The number of samples or volume of blood drawn must not be increased without prior approval of the relevant ethics committee.

Option 2: If it appears from pharmacokinetic measurements that oral absorption is extremely rapid, leading to a high Cmax with a relatively low AUC0-12, the dose may be split in half, with the second half being given 4-8 hours after the first. Under these circumstances, the blood sampling schedule would be decided prior to dosing but would not exceed 26 samples over a 120 hour period.

For Both Options:

  • Blood samples for analysis of metabolites will be drawn 4 and 8 hours after initial dosing.
  • Blood will be collected for safety measurements (haematology and clinical chemistry) 24, 48 and 72 hours post initial dosing.
  • Complete urine collections for analysis of F901318 urine concentration will be made for the following intervals in relation to dosing: 0-4, 4-8, 8-12, 12-16, 16-24, 24-48, 48-72, 72-96 and 96-120 hours after initial dosing.
  • Supine and standing pulse rate and blood pressure; and body temperature (vital signs) will be recorded 30, 60 and 120 minutes, 4, 8, 24, 48 and 72 hours after initial dosing.
  • Twelve-lead ECGs will be obtained 1, 4, 24, 48 and 72 hours after initial dosing.
  • The continuous ECG recording will cease 12 hours after initial dosing.
  • Spontaneously reported adverse events will be noted throughout.
  • A urine sample will be taken for urinalysis 24, 48 hours and 72 hours after initial dosing.
  • Lunch will be served approximately 4 hours after initial dosing but after all the 4 hour observations and blood sampling have been completed and a main meal will be served approximately 8 hours and a snack approximately 12 hours after dosing.

Subjects may leave the Research Unit on Day 6, unless they have experienced adverse events that, in the opinion of the Investigator, warrant further observation and/or treatment.

All subjects will be followed up 8-10 days after dosing with a post-study visit.


Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 46 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: F901318 - A Phase I, Double-Blind, Placebo Controlled, Single Ascending Oral Dose, Safety, Tolerability and Pharmacokinetic Study in Healthy Male Subjects
Study Start Date : October 2015
Actual Primary Completion Date : September 2016
Actual Study Completion Date : September 2016

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Aspergillosis

Arm Intervention/treatment
Experimental: Cohort A active
2 mg/kg orally F901318 safety,F901318 tolerability and F901318 pharmacokinetics
Drug: F901318 safety
Safety assessments
Other Name: adverse events

Drug: F901318 tolerability
Tolerability assessments
Other Name: adverse events

Drug: F901318 pharmacokinetics
Pharmacokinetic assessments
Other Name: metabolism

Placebo Comparator: Cohort A placebo
Matching placebo safety,placebo tolerability and placebo pharmacokinetics
Other: Placebo safety
Safety assessments
Other Name: adverse events

Other: Placebo tolerability
Placebo tolerability
Other Name: adverse events

Other: Placebo pharmacokinetics
Plaacebo pharmacokinetics
Other Name: metabolism

Experimental: Cohort B active
4 mg/kg orally F901318 safety,F901318 tolerability and F901318 pharmacokinetics
Drug: F901318 safety
Safety assessments
Other Name: adverse events

Drug: F901318 tolerability
Tolerability assessments
Other Name: adverse events

Drug: F901318 pharmacokinetics
Pharmacokinetic assessments
Other Name: metabolism

Placebo Comparator: Cohort B placebo
Matching placebo safety,placebo tolerability and placebo pharmacokinetics
Other: Placebo safety
Safety assessments
Other Name: adverse events

Other: Placebo tolerability
Placebo tolerability
Other Name: adverse events

Other: Placebo pharmacokinetics
Plaacebo pharmacokinetics
Other Name: metabolism

Experimental: Cohort C active
6 mg/kg orally F901318 safety,F901318 tolerability and F901318 pharmacokinetics
Drug: F901318 safety
Safety assessments
Other Name: adverse events

Drug: F901318 tolerability
Tolerability assessments
Other Name: adverse events

Drug: F901318 pharmacokinetics
Pharmacokinetic assessments
Other Name: metabolism

Placebo Comparator: Cohort C placebo
Matching placebo safety,placebo tolerability and placebo pharmacokinetics
Other: Placebo safety
Safety assessments
Other Name: adverse events

Other: Placebo tolerability
Placebo tolerability
Other Name: adverse events

Other: Placebo pharmacokinetics
Plaacebo pharmacokinetics
Other Name: metabolism

Experimental: Cohort D active
8 mg/kg orally F901318 safety,F901318 tolerability and F901318 pharmacokinetics
Drug: F901318 safety
Safety assessments
Other Name: adverse events

Drug: F901318 tolerability
Tolerability assessments
Other Name: adverse events

Drug: F901318 pharmacokinetics
Pharmacokinetic assessments
Other Name: metabolism

Placebo Comparator: Cohort D placebo
Matching placebo safety,placebo tolerability and placebo pharmacokinetics
Other: Placebo safety
Safety assessments
Other Name: adverse events

Other: Placebo tolerability
Placebo tolerability
Other Name: adverse events

Other: Placebo pharmacokinetics
Plaacebo pharmacokinetics
Other Name: metabolism

Experimental: Cohort E active
10 mg/kg orally F901318 safety,F901318 tolerability and F901318 pharmacokinetics
Drug: F901318 safety
Safety assessments
Other Name: adverse events

Drug: F901318 tolerability
Tolerability assessments
Other Name: adverse events

Drug: F901318 pharmacokinetics
Pharmacokinetic assessments
Other Name: metabolism

Placebo Comparator: Cohort E placebo
Matching placebo safety,placebo tolerability and placebo pharmacokinetics
Other: Placebo safety
Safety assessments
Other Name: adverse events

Other: Placebo tolerability
Placebo tolerability
Other Name: adverse events

Other: Placebo pharmacokinetics
Plaacebo pharmacokinetics
Other Name: metabolism




Primary Outcome Measures :
  1. Safety (Adverse events) [ Time Frame: 10 days ]
    Adverse events


Secondary Outcome Measures :
  1. Tolerability (Adverse events) [ Time Frame: 10 days ]
    Adverse events

  2. Pharmacokinetics (Area under concentration time curve, AUC) [ Time Frame: 120 hours ]
    Area under concentration time curve

  3. Pharmacokinetics (Cmax) [ Time Frame: 12 hours ]
    Cmax



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  1. Subjects will be males of any ethnic origin between 18 and 45 years of age and with a body weight of 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.

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 the dose administration 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 the dose administration (with the exception of vitamin/mineral supplements) 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 the dose administration 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.
  6. Subjects who have donated any blood, plasma or platelets in the 2 months prior to screening or who have made donations on more than two occasions within the 12 months preceding the dose administration.
  7. Subjects with a significant history of drug allergy as determined by the Investigator.
  8. Subjects who have any clinically significant allergic disease (excluding non-active hay fever) as determined by the Investigator.
  9. Subjects who have a supine blood pressure and supine pulse rate higher than 140/90 mmHg and 100 beats per minute (bpm), respectively, or lower than 90/50 mmHg and 40 bpm, respectively, confirmed by a repeat assessment.
  10. Subjects who consume more than 28 units of alcohol per week or who have a significant history of alcoholism or drug/chemical abuse as determined by the Investigator (one unit of alcohol equals ½ pint [285 mL] of beer or lager, one glass [125 mL] of wine, or 1/6 gill [25 mL] of spirits).
  11. Subjects with a positive urine drug screen or alcohol breath test result at screening or first admission.
  12. Subjects must not have smoked for 3 months prior to first dose administration unless otherwise specified by the Investigator or Sponsor.
  13. Subjects with, or with a history of, any clinically significant neurological, gastrointestinal, renal, hepatic, cardiovascular, psychiatric, respiratory, metabolic, endocrine, ocular (including minor trauma) haematological or other major disorders as determined by the Investigator.
  14. Subjects who are known to have serum hepatitis, or who are carriers of the hepatitis B surface antigen (HBsAg) or hepatitis C antibody, or who have a positive result to the test for HIV antibodies.
  15. Subjects who have an abnormality in the 12-lead ECG that, in the opinion of the Investigator, increases the risk of participating in the study, such as QTcB interval >430 msec, 2nd or 3rd degree atrioventricular block, complete left bundle branch block, complete right bundle branch block or Wolff-Parkinson-White Syndrome, defined as PR<110 msec, confirmed by a repeat ECG.
  16. Subjects who, in the opinion of the Investigator, should not participate in the study for any other reason.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02394483


Locations
Layout table for location information
United Kingdom
Simbec Orion
Merthyr Tydfil, Wales, United Kingdom, CF48 4DR
Sponsors and Collaborators
F2G Ltd.
Simbec-Orion Research
Investigators
Layout table for investigator information
Principal Investigator: Girish Sharma Simbec Orion Ltd

Layout table for additonal information
Responsible Party: F2G Ltd.
ClinicalTrials.gov Identifier: NCT02394483     History of Changes
Other Study ID Numbers: F901318-01-03-15
First Posted: March 20, 2015    Key Record Dates
Last Update Posted: September 19, 2016
Last Verified: August 2016

Keywords provided by F2G Ltd.:
Single ascending dose
double blind

Additional relevant MeSH terms:
Layout table for MeSH terms
Aspergillosis
Mycoses
Olorofim
Antifungal Agents
Anti-Infective Agents