Pharmacokinetics and Pharmacodynamics of Edoxaban Before and After Bariatric Surgery (EXPOSE)

Pharmacokinetics and Pharmacodynamics of Edoxaban in Subjects With Severe Obesity Before and After Sleeve Gastrectomy and Roux-en-Y Gastric Bypass

The study will be conducted at a single site in the Canada, Quebec. Participants will be recruited from the bariatric surgery clinic and will be required to be either, waiting for sleeve gastrectomy surgery (n=12, restrictive bariatric surgery, Group 1) or Roux-en-Y gastric bypass (n=12, mixed bariatric surgery, Group 1), or had underwent Roux-en-Y gastric bypass 12 ± 3 months ago (n=12, Group 2).

Participants in Group 1, edoxaban pharmacokinetic and pharmacodynamics will be evaluated before and 48 ± 5 hours after bariatric surgery (sleeve gastrectomy and Roux-en-Y gastric bypass). Participants in Group 2, edoxaban pharmacokinetic and pharmacodynamics will be evaluated only once, at 12 ± 3 months following their Roux-en-Y gastric bypass.

All participants will be received single oral doses of 60 mg edoxaban at each pharmacokinetic and pharmacodynamics evaluation.

Study Overview

• Status: Withdrawn
• Conditions: Bariatric Surgery Candidate
• Intervention / Treatment: Drug: Edoxaban Pharmacokinetics and Pharmacodynamics

Detailed Description

Screening visit (Group 1 and 2: visit 1) // Group 1: Screening will take place within 3 to 4-months window before bariatric surgery. Group 2: Screening will take place within 1-months window approximately 12± 3 months after bariatric surgery.

Informed consent will be obtained from the subject prior to performing any of the screening assessments.

The following activities and/or assessments will be performed at/during Screening: Informed consent, Inclusion/exclusion criteria, Medical history, Concomitant medications, Physical examination, including height, weight, and body mass index (BMI), Blood and urine samples, 12-lead ECG, Vital signs.

Pharmacokinetic (PK) and pharmacodynamics (PD) visit Group 1: PK and PD visit will take place after the screening visit and within 3-months window before bariatric surgery as well as 48 hours after bariatric surgery.

Group 2: PK and PD visit will take place after the screening visit and within 1-months window after bariatric surgery (12± 3 months).

On PK and PD visit, the following procedures will be performed: Vital signs, ECG, Concomitant medications, Edoxaban dosing (before 8:00 AM), Pharmacokinetics (PK) and Pharmacodynamics (PD) blood draws (predose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12 and 24 hours), Post dose fasting and water restrictions, as appropriate, Adverse event (AE) monitoring.

Follow-up 1 - Group 1 and Group 2: Follow-up 1 will take place onsite 24 hours after PK and PD visits.

On follow-up 1, the following procedures will be performed: PK and PD blood draws, Concomitant medications, AE monitoring.

Follow-up 2 - Group 1 and Group 2: Follow-up 2 will be a phone contact and will take place 7 days after PK and PD visits.

On follow-up 2, the following procedures will be performed: Concomitant medications, AE monitoring.

• Study Type: Interventional
• Phase: Phase 1

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

1. Male and female subjects over 18 years of age.

2. Females who are of non-childbearing potential must be:

   • Surgically sterile (i.e., bilateral tubal ligation or removal of both ovaries and/or uterus at least 6 months prior to dosing).
   • Naturally postmenopausal (spontaneous cessation of menses) for at least 12 consecutive months prior to screening visit, with a follicle stimulating hormone level in the postmenopausal range.
3. Females of childbearing potential must have a negative urine pregnancy test at each study visit with PK and PD evaluation.
4. Subjects must agree not to donate blood, plasma, platelets, or any other blood components for 4 weeks before each study visit with PK and PD evaluation.
5. Subjects must agree to food and drug restrictions during the study.
6. Subjects must agree to abstain from alcohol, cola, tea, coffee, chocolate, and other caffeinated drink and food from 2 days before each study visit with PK and PD evaluation.
7. Subjects must agree to abstain from food and beverages containing grapefruit, grapefruit juice, cranberry juice, lime, pomelo, marmalade and Seville oranges from 10 days before each study visit with PK and PD evaluation.
8. Absence of clinically significant deviations from medical history, physical examination and 12-lead ECG, as deemed by the Investigator, prior to enrollment.
9. Subject must have sinus rhythm on the 12-lead ECG at each study visit with PK and PD evaluation.
10. Has given written informed consent prior to participating in the study.
11. Able to understand and willing to comply with all study requirements, and willing to allow the collection of all blood specimens.
12. Normal coagulation values from INR (< 1.2).

Exclusion Criteria:

1. History or current evidence of clinically significant cardiac, hepatic, renal, pulmonary, endocrine, neurologic, infectious, gastrointestinal, hematologic, or oncologic disease as determined by screening medical history, physical examination, or 12-lead ECG.
2. Subjects with QTcF interval duration > 450 msec for males and >470 for females.
3. Subjects with abnormal waveform morphology on any of the ECGs at the screening that would preclude accurate measurement of the QT interval duration.
4. Subjects with a resting systolic (treated) blood pressure > 159 mmHg or < 90 mmHg or a diastolic blood pressure > 95 mmHg or < 50 mmHg.
5. History of malignancy.
6. Subjects who have had a clinically significant illness within 4 weeks prior to the first dose.
7. Subjects who have used any drugs or substances known to be strong inhibitors or strong inducers of CYP 3A4/5 enzymes or P-gp within 28 days prior to the first dosing.
8. Subjects with history of major bleeding, major trauma, or major surgical procedure of any type within 6 months of dosing.
9. Subjects with history of peptic ulcer, gastrointestinal bleeding (including hematemesis, melena, rectal bleeding) or bleeding from hemorrhoids.
10. Subjects with history of thrombophlebitis or pulmonary embolism.
11. Subjects with history of minor bleeding episodes such as epistaxis, rectal bleeding (spots of blood on toilet paper), and gingival bleeding within 3 months before the first dose.
12. Subjects who have any family history (suspected or documented) of coagulopathy.
13. Females with a history of dysfunctional uterine bleeding, including history of menorrhagia (heavy menstrual bleeding), metrorrhagia, or polymenorrhea.
14. Subjects with eye surgeries or trauma to the head or eye within 14 days of the first dose.
15. Subjects who have used fish oil, acetylsalicylic acid, any over-the-counter medication containing acetylsalicylic acid, nonsteroidal anti-inflammatory drugs (NSAIDs), or other supplements (e.g., gingko biloba, …) that could prolong bleeding within 14 days of the first dose or expect to use these during the study.
16. Subjects who have used anticoagulants (i.e., warfarin, low molecular weight heparin [LMWH]), coagulants, anti-platelet (i.e., clopidogrel) 30 days prior to the first dose.
17. Subjects with abnormal complete blood count at screening.
18. Subjects with estimated glomerular filtration rate (eGFR) < 60 mL/min/1.73m2.
19. Subject is currently enrolled in or has not yet completed at least 30 days or 5 half-lives, whichever is longer, since ending another investigational device or drug study or is receiving other investigational agents.
20. Subjects who, in the opinion of the Investigator, should not participate in the study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: Non-Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Group 1 - Roux en Y gastric bypass and Sleeve Gastrectomy; Edoxaban pharmacodynamic and pharmacokinetic will be evaluated before and 48 ± 5 hours after bariatric surgery (sleeve gastrectomy and Roux-en-Y gastric bypass).	Drug: Edoxaban Pharmacokinetics and Pharmacodynamics; Participants will be received single oral doses of edoxaban 60 mg.
Experimental: Group 2 - Roux en Y gastric bypass; Edoxaban pharmacodynamic and pharmacokinetic will be evaluated at 12 ± 3 months following Roux-en-Y gastric bypass surgery.	Drug: Edoxaban Pharmacokinetics and Pharmacodynamics; Participants will be received single oral doses of edoxaban 60 mg.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pharmacokinetics edoxaban parameter	Maximum edoxaban plasma concentration	0 hour (before taking edoxaban) - 0.5 hours - 1 hour - 1.5 hours - 2 hours - 2.5 hours - 3 hours - 4 hours - 6 hours - 8 hours - 12 hours - and 24 hours after taking edoxaban
Pharmacokinetics edoxaban parameter	Time to reach maximum edoxaban plasma concentration	0 hour (before taking edoxaban) - 0.5 hours - 1 hour - 1.5 hours - 2 hours - 2.5 hours - 3 hours - 4 hours - 6 hours - 8 hours - 12 hours - and 24 hours after taking edoxaban
Pharmacokinetics edoxaban parameter	Area under the edoxaban plasma concentration-time curve	0 hour (before taking edoxaban) - 0.5 hours - 1 hour - 1.5 hours - 2 hours - 2.5 hours - 3 hours - 4 hours - 6 hours - 8 hours - 12 hours - and 24 hours after taking edoxaban
Pharmacokinetics edoxaban parameter	Edoxaban half time	0 hour (before taking edoxaban) - 0.5 hours - 1 hour - 1.5 hours - 2 hours - 2.5 hours - 3 hours - 4 hours - 6 hours - 8 hours - 12 hours - and 24 hours after taking edoxaban

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Pharmacodynamics edoxaban parameter	aPTT	0 hour (before taking edoxaban) - 0.5 hours - 1 hour - 1.5 hours - 2 hours - 2.5 hours - 3 hours - 4 hours - 6 hours - 8 hours - 12 hours - and 24 hours after taking edoxaban
Pharmacodynamics edoxaban parameter	PT/INR	0 hour (before taking edoxaban) - 0.5 hours - 1 hour - 1.5 hours - 2 hours - 2.5 hours - 3 hours - 4 hours - 6 hours - 8 hours - 12 hours - and 24 hours after taking edoxaban
Pharmacodynamics edoxaban parameter	anti-FXa activity	0 hour (before taking edoxaban) - 0.5 hours - 1 hour - 1.5 hours - 2 hours - 2.5 hours - 3 hours - 4 hours - 6 hours - 8 hours - 12 hours - and 24 hours after taking edoxaban

Collaborators and Investigators

• Sponsor: Institut universitaire de cardiologie et de pneumologie de Québec, University Laval
• Investigators: Principal Investigator: Paul Poirier, MD, Phd, Institut universitaire de cardiologie et de pneumologie de Québec, University Laval

Study record dates

Study Major Dates

• Study Start (Actual): March 11, 2024
• Primary Completion (Actual): March 11, 2024
• Study Completion (Actual): March 11, 2024

Study Registration Dates

• First Submitted: March 11, 2024
• First Submitted That Met QC Criteria: March 21, 2024
• First Posted (Actual): March 22, 2024

Study Record Updates

• Last Update Posted (Actual): March 22, 2024
• Last Update Submitted That Met QC Criteria: March 21, 2024
• Last Verified: March 1, 2024

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Protease Inhibitors; Factor Xa Inhibitors; Antithrombins; Serine Proteinase Inhibitors; Anticoagulants; Edoxaban
• Other Study ID Numbers: 22121

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No