Bioavailability and Pharmacokinetics Study of FDL169 in Healthy Subjects and Subjects With Cystic Fibrosis

• ClinicalTrials.gov Identifier: NCT02767297
• Recruitment Status: Completed
• First Posted: May 10, 2016
• Last Update Posted: October 24, 2016
• Sponsor: Flatley Discovery Lab LLC
• Information provided by (Responsible Party): Flatley Discovery Lab LLC

Study Description

Brief Summary:

To determine the relative bioavailability of the capsule (reference) and tablet (test) formulations of FDL169 in healthy adult males and females, and to evaluate the pharmacokinetic (PK) profile FDL169 tablets (test formulation) in both healthy adult males and females, and subjects with cystic fibrosis (CF).

Condition or disease	Intervention/treatment	Phase
Cystic Fibrosis	Drug: FDL169	Phase 1; Phase 2

Detailed Description:

This is a three-part study.

Part 1:

Part 1 of the study is a single dose, open-label, randomized crossover study in healthy male and female subjects to compare the relative bioavailability of two formulations of FDL169.

Part 2:

Part 2 of the study is a multiple, escalating dose study of three different doses of the test formulation of FDL169 in healthy male and female subjects to evaluate the PK profile of the test formulation of FDL169.

Part 3:

Part 3 of the study is a single dose, open-label study in male and female subjects with CF to determine the PK profile of the test formulation of FDL169.

Study Design

• Study Type: Interventional (Clinical Trial)
• Actual Enrollment: 46 participants
• Allocation: Non-Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Official Title: A Three-Part Phase 1b Bioavailability and Pharmacokinetics Study of Two Formulations of FDL169 in Healthy Subjects and Subjects With Cystic Fibrosis
• Study Start Date: April 2016
• Actual Primary Completion Date: October 2016
• Actual Study Completion Date: October 2016

Arms and Interventions

Arm	Intervention/treatment
Experimental: Part 1: Single dose (cross over); FDL169 reference formulation and test formulation administered as a single dose in healthy subjects	Drug: FDL169
Experimental: Part 2: Multiple dose (dose level 1); FDL169 test formulation (Dose level 1) administered as repeat doses in healthy subjects	Drug: FDL169
Experimental: Part 2: Multiple dose (dose level 2); FDL169 test formulation (Dose level 2) administered as repeat doses in healthy subjects	Drug: FDL169
Experimental: Part 2: Multiple dose (dose level 3); FDL169 test formulation (Dose level 3) administered as repeat doses in healthy subjects	Drug: FDL169
Experimental: Part 3: Single dose; FDL169 test formulation administered as a single dose in CF subjects	Drug: FDL169

Outcome Measures

Primary Outcome Measures :

1. Part 1: Maximum plasma concentration of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 72 h post-dose ]
2. Part 1: Time to maximum plasma concentration of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 72 h post-dose ]
3. Part 1: Individual estimate of the terminal elimination rate constant of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 72 h post-dose ]
4. Part 1: Terminal half-life of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 72 h post-dose ]
5. Part 1: AUC from the time of dosing to the time of the last observed concentration for FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 72 h post-dose ]
6. Part 1: AUC extrapolated to infinity from dosing time, based on the last observed concentration for FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 72 h post-dose ]
7. Part 1: Clearance of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 72 h post-dose ]
8. Part 1: AUC% extrapolated for FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 72 h post-dose ]
9. Part 2: Maximum plasma concentration of FDL169 (and metabolites) following multiple oral doses of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post last dose ]
10. Part 2: Time to maximum plasma concentration of FDL169 (and metabolites) following multiple oral doses of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post last dose ]
11. Part 2: Individual estimate of the terminal elimination rate constant of FDL169 (and metabolites) following multiple oral doses of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post last dose ]
12. Part 2: Terminal half-life of FDL169 (and metabolites) following multiple oral doses of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post last dose ]
13. Part 2: AUC from the time of dosing to the time of the last observed concentration for FDL169 (and metabolites) following multiple oral doses FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post last dose ]
14. Part 2: AUC extrapolated to infinity from dosing time, based on the last observed concentration for FDL169 (and metabolites) following multiple oral doses of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post last dose ]
15. Part 2: Clearance of FDL169 (and metabolites) following multiple oral doses of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post last dose ]
16. Part 2: AUC% extrapolated for FDL169 (and metabolites) following multiple oral doses of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post last dose ]
17. Part 3: Maximum plasma concentration of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post-dose ]
18. Part 3: Time to maximum plasma concentration of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post-dose ]
19. Part 3: Individual estimate of the terminal elimination rate constant of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post-dose ]
20. Part 3: Terminal half-life of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post-dose ]
21. Part 3: AUC from the time of dosing to the time of the last observed concentration for FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post-dose ]
22. Part 3: AUC extrapolated to infinity from dosing time, based on the last observed concentration for FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post-dose ]
23. Part 3: Clearance of FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post-dose ]
24. Part 3: AUC% extrapolated for FDL169 (and metabolites) following single oral dose of FDL169 [ Time Frame: Multiple points from pre-dose to 48 h post-dose ]

Secondary Outcome Measures :

1. Number of subjects with clinically significant changes in systolic and diastolic blood pressure following single and multiple oral doses of FDL169 [ Time Frame: Multiple points from screening to follow-up (7 days after last dose) ]
2. Number of subjects with clinically significant changes in heart rate following single and multiple oral doses of FDL169 [ Time Frame: Multiple points from screening to follow-up (7 days after last dose) ]
3. Number of subjects with clinically significant changes in oral temperature following single and multiple oral doses of FDL169 [ Time Frame: Multiple points from screening to follow-up (7 days after last dose) ]
4. Number of subjects with clinically significant changes in oxygen saturation following single and multiple oral doses of FDL169 [ Time Frame: Multiple points from screening to follow-up (7 days after last dose) ]
5. Number of subjects with clinically significant 12-lead ECG abnormalities following single and multiple oral doses of FDL169 [ Time Frame: Multiple points from screening to follow-up (7 days after last dose) ]
6. Number of subjects with abnormal laboratory values following single and multiple oral doses of FDL169 [ Time Frame: Multiple points from screening to follow-up (7 days after last dose) ]
7. Number of subjects experiencing treatment-related adverse events following single and multiple oral doses of FDL169 [ Time Frame: Multiple points from screening to follow-up (7 days after last dose) ]

Eligibility Criteria

• Ages Eligible for Study: 18 Years and older (Adult, Older Adult)
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Criteria

Inclusion Criteria:

Parts 1 and 2:

1. Healthy, males and females between 18 and 55 years of age, inclusive, with a BMI of >19 and <30 kg/m2.
2. If sexually active, must meet the contraception requirements.

Part 3:

1. Male and female subjects aged 18 years and older.
2. If sexually active, must meet the contraception requirements.
3. Diagnosis of CF.
4. History of pancreatic insufficiency.
5. Forced expiratory volume in 1 second (FEV1) ≥40% of predicted normal for age, sex and height at screening.

Exclusion Criteria:

Parts 1 and 2:

1. Prior or ongoing medical condition, medical history, physical findings, ECG findings or laboratory abnormality that could adversely affect the safety of the subject.
2. Alkaline phosphatase, aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) level >1.5 x upper limit of normal (ULN) at screening.
3. Use of prescription or non-prescription drugs within 21 days or five half-lives (whichever is longer) before the first dose of study medication, unless the medication will not interfere with the study procedures or compromise subject safety.
4. Pregnant or nursing females.
5. Serum creatinine or total bilirubin >1.5 x ULN (isolated bilirubin >1.5 x ULN is acceptable if bilirubin is fractionated and direct bilirubin is <35%).
6. History of prolonged QT and/or QTcF interval.
7. ECG with a single QTcF >450 msec in males, >460 msec in females, at Screening.
8. Positive urinary drugs of abuse screen at Screening or Day -1, or positive alcohol screen at Day -1.
9. History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of >21 units.
10. History of human immunodeficiency virus (HIV) or positive HIV, hepatitis B or hepatitis C results at screening.
11. Donation of 500 mL or more blood within 3 months before Day -1.
12. Participation in a clinical trial involving receipt of an investigational product within the past 90 days or exposure to more than four new chemical entities with 12 months of the first dosing day.
13. Current smoking or use of tobacco products or substitutes. Former smokers will be eligible, provided they have not smoked for at least 6 months before Day -1.
14. Use of any prescription and non-prescription medications that are inhibitors or inducers of cytochrome P450 (CYP) 3A4 within 7 days before Day -1.

Part 3:

1. History of any illness, or ongoing acute illness that could impact the safety of the subject or confound study results.
2. Abnormal liver function ≥3 x ULN: AST, ALT, total bilirubin.
3. A pulmonary exacerbation, or changes in therapy for pulmonary disease within 4 weeks prior to the Baseline (Day 1) Visit
4. Use of herbal and dietary supplements within 21 days or five half-lives (whichever is longer) before the first dose of study medication, unless the medication will not interfere with the study procedures or compromise subject safety.
5. Pregnant or nursing females.
6. Serum creatinine or total bilirubin >1.5 x ULN (isolated bilirubin >1.5 x ULN is acceptable if bilirubin is fractionated and direct bilirubin is <35%).
7. History of prolonged QT and/or QTcF interval.
8. ECG with a single QTcF >450 msec in males, >460 msec in females, at Screening.
9. Positive urinary drugs of abuse screen at Screening or Day -1, or positive alcohol screen at Day -1.
10. History of regular alcohol consumption within 6 months of the study defined as an average weekly intake of >21 units.
11. History of HIV, or positive HIV, hepatitis B or hepatitis C results at screening.
12. Donation of 500 mL or more blood within 3 months before Day -1.
13. Participation in a clinical trial involving receipt of an investigational product within the past 90 days or exposure to more than four new chemical entities with 12 months of the first dosing day.
14. Current smoking or use of tobacco products or substitutes. Former smokers will be eligible, provided they have not smoked for at least 6 months before Day -1.
15. Use of any prescription and non-prescription medications that are inhibitors or inducers of CYP3A4, within 7 days before Day -1.

Contacts and Locations

Locations

United Kingdom

Celerion

Belfast, United Kingdom, BT9 6AD

Sponsors and Collaborators

Flatley Discovery Lab LLC

Investigators

• Principal Investigator: Stuart Elborn, MD; Queen's University

More Information

• Responsible Party: Flatley Discovery Lab LLC
• ClinicalTrials.gov Identifier: NCT02767297 History of Changes
• Other Study ID Numbers: FDL169-2015-03
• First Posted: May 10, 2016
• Last Update Posted: October 24, 2016
• Last Verified: October 2016

Individual Participant Data (IPD) Sharing Statement:

• Plan to Share IPD: Undecided

Additional relevant MeSH terms:

Cystic Fibrosis; Fibrosis; Pathologic Processes; Pancreatic Diseases; Digestive System Diseases; Lung Diseases; Respiratory Tract Diseases; Genetic Diseases, Inborn; Infant, Newborn, Diseases