Pharmacokinetics of Tasimelteon in Subjects With Renal Impairment and Matched Control Subjects With Relatively Normal Renal Function

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Vanda Pharmaceuticals
ClinicalTrials.gov Identifier:
NCT01526746
First received: January 26, 2012
Last updated: February 14, 2014
Last verified: February 2014
  Purpose

The purpose of this research study is to understand whether there is any difference in the amount of tasimelteon (including its breakdown products) in the blood of individuals with severe renal impairment compared to individuals who have normal renal function. The safety and tolerability of tasimelteon will also be assessed throughout this study.


Condition Intervention Phase
Renal Impairment
Drug: Tasimelteon
Phase 1

Study Type: Interventional
Study Design: Allocation: Non-Randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Basic Science
Official Title: An Open-Label, Single-Dose, Parallel-Group Study to Compare the Pharmacokinetics of Tasimelteon in Subjects With Renal Impairment With That in Matched Control Subjects With Relatively Normal Renal Function

Resource links provided by NLM:


Further study details as provided by Vanda Pharmaceuticals:

Primary Outcome Measures:
  • Tasimelteon pharmacokinetic parameters (AUC, Cmax, Tmax) [ Time Frame: Predose, 0.25, 1, 1.5, 2, 4, 6, 8, 12, 24, 30, and 36 hours post-dose ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Pharmacokinetic parameters (AUC, Cmax, Tmax) of tasimelteon metabolites M3, M9, M11, M12, M13, and M14 [ Time Frame: Predose, 0.25, 1, 1.5, 2, 4, 6, 8, 12, 24, 30, and 36 hours post-dose ] [ Designated as safety issue: No ]
  • The percentage of tasimelteon and its metabolites that are removed by hemodialysis (AUC) [ Time Frame: 4, 6, 8 hours after dosing ] [ Designated as safety issue: No ]
    paired arterial and venous samples

  • The ratio of plasma protein bound versus unbound fractions of tasimelteon and metabolites M9, M11, M12, M13, and M14 [ Time Frame: 0.5 and 3 hours post dose ] [ Designated as safety issue: No ]
  • Safety and tolerability as measured by spontaneous reporting of AEs, and clinically significant changes in laboratory parameters, ECG parameters, and vital signs [ Time Frame: 36 hours ] [ Designated as safety issue: Yes ]
  • The Columbia-Suicide Severity Rating Scale will be used to assess suicidal behavior and ideation. [ Time Frame: once per day at Screening (approximately day -7), Day -1 (baseline), Day 2 (end of study) ] [ Designated as safety issue: Yes ]

Enrollment: 32
Study Start Date: February 2012
Study Completion Date: June 2012
Primary Completion Date: June 2012 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: End Stage Renal Disease, dialysis
eGFR <15 ml/min/1.73m^2
Drug: Tasimelteon
20mg capsule, once
Other Name: VEC-162
Drug: Tasimelteon
20mg, once
Experimental: Severe renal impairment
eGFR < 29 ml/min/1.73m^2
Drug: Tasimelteon
20mg capsule, once
Other Name: VEC-162
Drug: Tasimelteon
20mg, once
Experimental: Healthy controls
eGFR > 80 mL/min/1.73m^2 Matched to renally impaired subjects by age, gender, BMI, and smoking status
Drug: Tasimelteon
20mg capsule, once
Other Name: VEC-162
Drug: Tasimelteon
20mg, once

  Eligibility

Ages Eligible for Study:   18 Years to 79 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

Groups 1-3

  1. Ability and acceptance to provide written informed consent;
  2. Men or women between 18 - 79 years, inclusive;
  3. Subjects with Body Mass Index (BMI) of >18 and <40 kg/m2 (BMI = weight (kg)/ [height (m)]2);
  4. Males, non-fecund females (i.e., surgically sterilized, if procedure was done 6 months before screening or subject is postmenopausal, without menses for 6 months before screening), or females of child-bearing potential using an acceptable method of birth control for a period of 35 days before the first dosing and have a negative pregnancy test at the screening and baseline visits; Note 1: Acceptable methods of birth control include any one of the following: abstinence, vasectomized sexual partner, hormonal methods (i.e. pill, hormonal IUD, Depo-Provera, implants, patch, intravaginal device [NuvaRing]), intrauterine device (IUD [copper banded coils]), diaphragm, cervical cap, or condom with spermicidal jelly or foam.
  5. Willing and able to comply with study requirements and restrictions;

Groups 1- 2 (renal impairment)

  1. Subjects with renal impairment defined as

    1. Group 1: Stage 5 End Stage Renal Disease (ESRD) (eGFR < 15 mL/min/m2) requiring regularly scheduled dialysis and have been on a stable dialysis regimen for at least three months at baseline; OR
    2. Group 2: Stage 4 severe renal impairment (eGFR ≤ 29 mL/min/m2) but not requiring dialysis as calculated using the Modification of Diet in Renal Disease (MDRD) Equation (Appendix 18.3)
  2. Otherwise considered healthy in general as determined by past medical history, physical examination, vital signs, electrocardiogram, and laboratory tests at screening;
  3. Vital signs (after 3 minutes resting in a semi-supine position) which are within the ranges shown below.

    1. Body temperature between 35.0-37.5 °C;
    2. Systolic blood pressure between 100-180 mmHg;
    3. Diastolic blood pressure between 60-115 mmHg;
    4. Pulse rate between 40-100 bpm.

Group 3 (healthy matched controls)

  1. Subjects in Group 3 must match in gender, smoking status, age (±10 years), and body mass index [normal BMIs (18.00-24.99), overweight BMIs (25.00-30.99) and obese BMIs (31.00-40.00)] to Group 1 and/or 2;
  2. Subjects must have normal renal function defined as eGFR ≥ 80 mL/min/m2 as calculated using the Modification of Diet in Renal Disease (MDRD) Equation (Appendix 18.3 );
  3. Subjects must be in good health as determined by past medical history, physical examination, electrocardiogram, laboratory tests and urinalysis;
  4. Vital signs (after 3 minutes resting in a semi-supine position) which are within the ranges shown below:

    1. Body temperature between 35.0 - 37.5 °C;
    2. Systolic blood pressure between 90 - 150 mmHg;
    3. Diastolic blood pressure between 50 - 95 mmHg;
    4. Pulse rate between 40 - 90 bpm.

Exclusion Criteria:

Groups 1-3

  1. Smokers (use of tobacco products in the previous 3 months) unable or unwilling to limit consumption to 10 cigarettes per day or less while checked into the inpatient facility.

    a. Note: Smoking will be a match criteria and the site should attempt to enroll an equal number of smokers and non-smokers into each group.

  2. Exposure to any investigation drug, including placebo, within 30 days or 5 half-lives (whichever is longer) of dosing;
  3. Donation or loss of 400 mL or more of blood within two months prior to dosing;
  4. Significant illness within the two weeks prior to dosing;
  5. Answer 'yes' to either Question 4 (Active Suicidal Ideation with Some Intent to Act, Without Specific Plan) or Question 5 (Active Suicidal Ideation with Specific Plan and Intent) on the "Suicidal Ideation" portion of the C-SSRS, or answer "yes" to any of the suicide-related behaviors (actual attempt, interrupted attempt, aborted attempt, preparatory act, or behavior) on the "Suicidal Behavior" portion of the Columbia Suicide Severity Rating Scale (C-SSRS); and the ideation or behavior occurred within the past 6 months;
  6. Functioning renal transplant;
  7. History within the past 2 years of clinically significant acute or chronic bronchospastic disease, including asthma and chronic obstructive pulmonary disease, treated or not treated;
  8. Treatment with any drug known to cause major organ system toxicity (e.g., chloramphenicol or tamoxifen) during the 60 day preceding the Screening visit;
  9. Participation in a previous BMS-214778/VEC-162 trial;
  10. History of drug or alcohol abuse as defined in DSM-IV, Diagnostic Criteria for Drug and Alcohol Abuse, within the 12 months prior to screening or evidence of such abuse as indicated by the laboratory assays conducted during the screening and baseline visits. A positive drug screen in Groups 1 and 2 is acceptable if there is documentation that subjects have been prescribed the corresponding medication;
  11. History of immunocompromise, including a positive HIV (ELISA and Western blot) test result;
  12. A positive Hepatitis B surface antigen (HBsAg) test result;
  13. Any surgical or medical condition which might significantly alter the absorption, distribution or excretion of any drug. The Investigator should be guided by evidence of any of the following:

    1. History of clinically significant inflammatory bowel syndrome, gastritis, ulcers, gastrointestinal or rectal bleeding;
    2. History of major gastrointestinal tract surgery such as gastrectomy, gastroenterostomy, or bowel resection;
    3. History of pancreatic injury or pancreatitis;
    4. History or presence of liver disease or liver injury as indicated by lab values such as SGOT, SGPT, GGT, alkaline phosphatase, or serum bilirubin 1.5 times greater than the upper limit of normal;
  14. Clinically significant ECG abnormalities or vital sign abnormalities at screening or a history of unstable, severe, or clinically significant cardiovascular disease (e.g., myocardial infarction within previous 6 months, unstable angina, cardiac failure, second/third degree atrioventricular block);
  15. Subjects taking any unapproved prescription or over-the-counter medications; all concomitant medications must be discussed with and approved by the sponsor prior to enrollment;
  16. A known hypersensitivity to tasimelteon or drugs similar to tasimelteon including melatonin;
  17. Pregnant or lactating females;
  18. Inability to swallow the study medication whole;
  19. Any other sound medical reason as determined by the clinical Investigator.

Groups 1 - 2 (renal impairment)

  1. Subjects with clinically significant abnormal findings, not consistent with clinical disease, upon physical examination, ECG, or laboratory evaluation;
  2. Evidence of progressive renal disease within 4 weeks prior to screening;
  3. Acute renal failure or nephrotic syndrome;
  4. Current hematuria of urologic origin;
  5. Any significant change in chronic treatment medication as determined by the clinical Investigator.

Group 3 (healthy matched controls)

  1. Use of unapproved prescription medication within 1 month of dosing and OTC medication within 14 days prior to dosing;
  2. History or presence of impaired renal function as indicated by abnormal (>ULN) creatinine or BUN values or abnormal urinary constituents (e.g., albuminuria).
  3. A positive hepatitis C test result.
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01526746

Locations
United States, Florida
Clinical Pharmacology of Miami, Inc.
Miami, Florida, United States, 33014
Orlando Clinical Research Center
Orlando, Florida, United States, 32809
United States, Minnesota
DaVita Clinical Research
Minneapolis, Minnesota, United States
Sponsors and Collaborators
Vanda Pharmaceuticals
  More Information

No publications provided

Responsible Party: Vanda Pharmaceuticals
ClinicalTrials.gov Identifier: NCT01526746     History of Changes
Other Study ID Numbers: VP-VEC-162-1106
Study First Received: January 26, 2012
Last Updated: February 14, 2014
Health Authority: United States: Food and Drug Administration

Keywords provided by Vanda Pharmaceuticals:
End stage renal disease
ESRD
kidney disease
renal impairment
renal

Additional relevant MeSH terms:
Renal Insufficiency
Kidney Diseases
Urologic Diseases

ClinicalTrials.gov processed this record on August 26, 2014