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Phase IIb One Year Efficacy and Safety Study of S-2367 in Obese Subjects With Initial 6-Week Low Calorie Diet

Sponsor
Shionogi (Industry)
Overall Status
Completed
CT.gov ID
NCT00748605
Collaborator
(none)
842
Enrollment
40
Locations
3
Arms
19.1
Duration (Months)
21.1
Patients Per Site
1.1
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

  1. To evaluate the weight loss effect of 1600 mg/day S-2367 administered orally once daily with the morning meal after a 6-week low calorie diet (LCD) of 950 kcal/day with or without S-2367 followed by 54 weeks while on a 800 kcal deficit reduced calorie diet (RCD) compared with placebo in medically stable and otherwise healthy obese male and female subjects

  2. To evaluate the safety and tolerability of 1600 mg/day S-2367 administered orally once daily with the morning meal after a 6-week LCD with or without S-2367 followed by 54 weeks on a RCD compared with placebo in medically stable and otherwise healthy obese male and female subjects

  3. To evaluate the steady-state/trough pharmacokinetics of 1600 mg/day S-2367 administered orally once daily with the morning meal after a 6-week LCD with or without S-2367 followed by 54 weeks on a RCD in obese male and female subjects

  4. To evaluate the weight loss effect of 1600 mg/day S-2367 administered orally once daily with the morning meal during an initial 6-week LCD compared with placebo in medically stable and otherwise healthy obese male and female subjects

Condition or Disease Intervention/Treatment Phase
  • Drug: S-2367 Placebo
  • Drug: S-2367 1600 mg q.d. 54 Weeks
  • Drug: S-2367 1600 mg q.d. 60 weeks
  • Other: LCD (low calorie diet)
  • Other: RCD (reduced calorie diet)
 Phase 2

Study Design

Study Type:
Interventional
Actual Enrollment :
842 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
A Double-Blind, Multi-Center, Randomized, Parallel-Group, Yearlong Study to Assess the Efficacy and Safety of 0 or 1600 mg/Day of S-2367 Administered Orally Once Daily With an Initial 6-Week Low Calorie Diet in Obese Males and Females
Study Start Date :
Jun 1, 2007
Actual Primary Completion Date :
Nov 1, 2008
Actual Study Completion Date :
Jan 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Placebo

S-2367 placebo + LCD (Low Calorie Diet) +RCD (Reduced Calorie Diet)

Drug: S-2367 Placebo
Four placebo tablets (total dose = 0 mg/day S-2367) administered orally once daily with AM (ante meridiem) meal while on both LCD (low calorie diet for 6 weeks) and RCD (reduced calorie diet for 54 weeks) for a total of 60 weeks

Other: LCD (low calorie diet)
A low calorie diet was utilized during the first 6 weeks of the study

Other: RCD (reduced calorie diet)
A reduced calorie diet was used during the last 54 weeks for the study
Experimental: S-2367 1600 mg q.d. 54 weeks

S-2367 placebo + LCD for 6 weeks and 1600 mg S-2367 + RCD for 54 weeks

Drug: S-2367 Placebo
Four placebo tablets (total dose = 0 mg/day S-2367) administered orally once daily with AM (ante meridiem) meal while on both LCD (low calorie diet for 6 weeks) and RCD (reduced calorie diet for 54 weeks) for a total of 60 weeks

Drug: S-2367 1600 mg q.d. 54 Weeks
Four 400 mg S- 2367 tablets (total dose = 1600 mg/day S-2367) administered orally once daily with AM meal while on RCD for a total of 54 weeks
Other Names:
  • Velneperit

    • Other: LCD (low calorie diet)
    A low calorie diet was utilized during the first 6 weeks of the study

    Other: RCD (reduced calorie diet)
    A reduced calorie diet was used during the last 54 weeks for the study
    Experimental: S-2367 1600 mg q.d. 60 weeks

    S-23671600 mg q.d. + LCD for 6 weeks and S-2367 1600 mg q.d + RCD for 54 weeks

    Drug: S-2367 1600 mg q.d. 60 weeks
    Four 400 mg S- 2367 tablets (total dose = 1600 mg/day S-2367) administered orally once daily with AM meal while on both LCD and RCD for a total of 60 weeks
    Other Names:
  • Velneperit

    • Other: LCD (low calorie diet)
    A low calorie diet was utilized during the first 6 weeks of the study

    Other: RCD (reduced calorie diet)
    A reduced calorie diet was used during the last 54 weeks for the study

    Outcome Measures

    Primary Outcome Measures

    1. The change in body weight over the 60-week active therapy phase of the study [60 weeks]

    Secondary Outcome Measures

    1. Change in body composition: calculated body mass index, waist circumference, hip circumference, and calculated waist-to-hip ratio [Throughout the study]

    2. Steady-state/trough pharmacokinetic analysis [After 9, 18, 30, 42, and 60 weeks of study drug treatment]

    3. Safety and tolerability of S-2367: treatment emergent adverse events, clinical laboratory data, vital signs, and 12-lead electrocardiogram parameters at each visit [Throughout the study]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:

    • Males and females between 18 and 65 years of age and body mass index between 30.0 to 45.0 kg/m2, inclusive, and a weight that has not fluctuated by more than 3% for the last 3 months

    • Medically stable for 3 months prior to Visit 1 and in otherwise good health, with no clinically significant findings from medical history, physical examination, 12-lead electrocardiograms (ECGs), and vital signs

    • Clinical laboratory evaluations (including clinical chemistry [fasted at least 8 hours], complete blood count, urinalysis, including creatine phosphokinase, amylase, lipase, lipid profile, insulin, Homeostatic Model Assessment of Insulin Sensitivity Index, hemoglobin A1c, thyroid stimulating hormone, free thyroxine, cortisol, iron, and ferritin) within the reference range for the test laboratory, unless deemed not clinically significant by the investigator

    • Males will be sterile or agree to use an approved method of contraception. Some of the approved methods of contraception for males includes a surgically sterile (for at least 3 months prior to Visit 1) female sexual partner; a postmenopausal (for at least 1 year since last menstrual cycle) female sexual partner; a female sexual partner who uses (for at least previous 3 months prior to Visit 1 and during study) oral, implantable, transdermal, or injectable oral contraceptives; or use of the following double-barrier method: male condom with spermicide

    • Females will be non-pregnant, non-lactating, and either postmenopausal for at least 1 year since last menstrual period, surgically sterile for at least 3 months prior to Visit 1, or agree to use an approved method of contraception. Some of the approved methods of contraception for females include a sterile (for at least 3 months prior to Visit 1) male sexual partner; use of oral, implantable, transdermal, or injectable oral contraceptives; or use of one of the following double-barrier methods: intrauterine device with spermicide, diaphragm with spermicide, cervical cap with spermicide, female condom with spermicide, or a male condom with spermicide by the male sexual partner

    • Able to understand and willing to sign an informed consent form and comply with all study procedures

    Exclusion Criteria:

    • History or clinical manifestations of significant metabolic, hepatic, immunological (e.g., human immunodeficiency virus/ acquired immunodeficiency syndrome), renal, hematological, pulmonary, cardiovascular, gastrointestinal (GI), urological, neurological, or psychiatric disorders

    • History or presence of an abnormal ECG, which in the investigator's opinion, is clinically significant

    • History or evidence of a psychological disorder, other than stable or controlled anxiety or depression, including but not limited to the schizophrenias. Treatment with an antidepressant or anxiolytic drug(s) will be permitted if the dose and form has remained stable for at least the previous 3 months and the medication is not precluded/ excluded by this protocol because of potential effects on body weight and is not expected to change during the remainder of this clinical protocol

    • History or evidence of an eating disorder with a compensatory behavior such as "purging bulimia nervosa" or "non-purging bulimia nervosa"

    • History of obesity of endocrine origin

    • History of Type 1 or Type 2 diabetes mellitus

    • Clinically significant hypertension defined as blood pressure > 160/90 mm Hg for either the systolic or diastolic values in either the untreated or treated state

    • Clinically significant GI history or surgery. NOTE: Appendectomy and cholecystectomy will be allowed

    • Gastric bypass surgery, stomach banding surgery, or any other surgical procedure(s) that attempt to promote/aid weight loss

    • History of polycystic ovarian syndrome

    • History of fenfluramine or dexfenfluramine or "fen-phen" administration with abnormal findings on echocardiograms at the time of "fen-phen" discontinuation

    • History of participation in any weight loss program within 3 months prior to Visit 1

    • History of body weight loss or gain greater than 3% within 3 months prior to Visit 1

    • History of alcoholism or drug addiction/ substance abuse within 1 year prior to Visit 1

    • History of any tobacco-containing or nicotine-containing product use within 1 year prior to Visit 1

    • Participation in any other investigational study drug trial in which receipt of investigational study drug occurred within 3 months prior to Visit 1

    • Previous use or participation in a study of S-2367 or any other neuropeptide Y5 agonist or antagonist

    • Participation in any weight loss medication/product study in which receipt of weight loss medication/product occurred within 3 months prior to Visit 1

    • Use of any prescription or non-prescription over-the-counter (OTC) medication/product or herbal/phytotherapeutic/plant-derived medications/products within 3 months prior to Visit 1 that is intended to induce weight loss, appetite suppression, weight control, or treat obesity

    • Use of chronic medications/products within 3 months prior to Visit 1 or during the study that are known to cause weight gain. The list includes but is not limited to amitriptyline (Elavil), paroxetine (Paxil), setraline (Zoloft), and mirtazepine (Remeron)

    • Use of any prescription or non-prescription OTC medications/products within 1 month prior to Visit 1, unless deemed acceptable by the investigator.

    • Donation of blood or blood products 3 months prior to Visit 1 or during the entire study

    • Any acute or chronic condition that, in the opinion of the investigator, would limit the subject's ability to complete and/ or participate in this clinical study

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Birmingham Alabama United States 35209
    2 Huntsville Alabama United States 35801
    3 Phoenix Arizona United States 85014
    4 Fountain Valley California United States 92708
    5 San Diego California United States 92108
    6 San Francisco California United States 94102
    7 Waterbury Connecticut United States 06708
    8 Jacksonville Florida United States 32259
    9 Ocala Florida United States 34471
    10 Orlando Florida United States 32809
    11 South Miami Florida United States 33143
    12 Atlanta Georgia United States 30338
    13 Augusta Georgia United States 30904
    14 Boise Idaho United States 83704
    15 Chicago Illinois United States 60610
    16 Gurnee Illinois United States 60031
    17 Wichita Kansas United States 67207
    18 Lexington Kentucky United States 40509
    19 Boston Massachusetts United States 02135
    20 South Dartmouth Massachusetts United States 02747
    21 Brooklyn Center Minnesota United States 55430
    22 Kansas City Missouri United States 64114
    23 Saint Louis Missouri United States 63141
    24 Lincoln Nebraska United States 68510
    25 Las Vegas Nevada United States 89146
    26 Edison New Jersey United States 08817
    27 Endwell New York United States 13760
    28 Burlington North Carolina United States 27215
    29 Winston-Salem North Carolina United States 27103
    30 Cincinnati Ohio United States 45219
    31 Columbus Ohio United States 43212
    32 Yukon Oklahoma United States 73099
    33 Bensalem Pennsylvania United States 19020
    34 Mount Pleasant South Carolina United States 29464
    35 Nashville Tennessee United States 37203
    36 Fort Worth Texas United States 76135
    37 New Braunfels Texas United States 78130
    38 San Antonio Texas United States 78229
    39 West Jordan Utah United States 84088
    40 Wauwatosa Wisconsin United States 53226

    Sponsors and Collaborators

    • Shionogi

    Investigators

    • Study Director: Shionogi Clinical Trials Administrator Clinical Support Help Line, Shionogi

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Shionogi
    ClinicalTrials.gov Identifier:
    NCT00748605
    Other Study ID Numbers:
    • 0702A2824 revised
    First Posted:
    Sep 8, 2008
    Last Update Posted:
    May 11, 2018
    Last Verified:
    May 1, 2018
    Keywords provided by Shionogi
    Obesity
    Additional relevant MeSH terms:
    Obesity

    Study Results

    No Results Posted as of May 11, 2018