Study to Evaluate the Efficacy and Safety of Belviq XR® in Conjunction With Lifestyle Modification for Weight Loss in Obese Adolescents, Age 12 to 17 Years

NCT ID: NCT03338296

Last Updated: 2021-07-19

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE4
• Total Enrollment: 278 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-09-28
• Study Completion Date: 2020-04-03

Brief Summary

This study will be conducted to demonstrate weight loss efficacy by change in body mass index (BMI) and safety in adolescents age 12 to 17 years (inclusive) during 52 weeks of treatment with Belviq XR 20 milligrams (mg) administered once daily (QD) as compared to placebo.

Conditions

Obesity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Lorcaserin hydrochloride XR 20 mg QD

Participants will receive lorcaserin hydrochloride extended release (XR) 20 milligrams (mg) once daily (QD) for up to 52 weeks.

Group Type: EXPERIMENTAL

lorcaserin hydrochloride XR

Intervention Type: DRUG

oral tablet

Placebo

Participants will receive placebo QD for up to 52 weeks.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

oral tablet

Interventions

lorcaserin hydrochloride XR

oral tablet

Intervention Type: DRUG

Placebo

oral tablet

Intervention Type: DRUG

Other Intervention Names

Belviq XR®

Eligibility Criteria

Inclusion Criteria

• Healthy male or female adolescents, age 12 to 17 years (inclusive) at Screening, with a BMI that is greater than or equal to the United States-weighted mean of the 95th percentile based on age and sex with a body weight greater than 60 kilograms (kg). Participants with Type 2 diabetes mellitus (T2DM) may have a pre-existing or new diagnosis of T2DM.

Participants with pre-existing T2DM should have prior documentation consistent with the diagnosis and/or be on active pharmacotherapy for T2DM.

Participants with a new diagnosis of T2DM (ie, diagnosed at Screening) should be based on the 2016 American Diabetes Association (ADA) guidelines. The diagnostic criteria are met if a participant has unequivocal hyperglycemia (random plasma glucose ≥200 milligrams per deciliter (mg/dL) (11.1 millimoles per liter [mmol/L]) with classic symptoms of hyperglycemia or hyperglycemic crisis) OR any of the following criteria are observed and confirmed:

• HbA1c ≥6.5%
• fasting plasma glucose (FPG) ≥126 mg/dL (7.0 mmol/L)
• 2-hour plasma glucose ≥200 mg/dL (11.1 mmol/L) by an oral glucose tolerance test (OGTT) All T2DM participants must have an HbA1c <10% at Screening. If participants are being or need to be treated with antidiabetic agents, the T2DM treatment regimen must be stable for at least 3 months before randomization. A single rescreen is allowed following stabilization. Stable control refers to minimal dose changes to existing medications for glycemic control and no medications being initiated for glycemic control in the 3 months before randomization. Minimal changes are defined as a change without any change in dose frequency, no add-on or discontinuation of other antidiabetic agents and the participant has not been hospitalized due to hypo- or hyperglycemic events.

• Participants and their families not planning to move away from the area for the duration of the study
• Participants able and willing to comply with all aspects of the study, including a standardized, reduced calorie diet and an age appropriate, increased physical activity program
• Participants considered in stable health in the opinion of the investigator
• Caregivers or guardians meet the following requirements:

• Able and willing to support and supervise study participation in the opinion of the investigator, including consideration of any existing physical, medical, or mental condition that prevents compliance with the protocol
• Able and willing to personally comply with and execute all aspects of the study requirements for the caregivers or guardians

Exclusion Criteria

• Clinically significant new illness within 1 month before randomization that may affect the participant's ability to fulfill the study requirements or significantly confound the assessments
• Participants who cannot swallow investigational products
• Participants with T2DM who have hypoglycemia unawareness
• Any of the following findings on Screening echocardiography:

• Aortic regurgitation mild or greater
• Mitral regurgitation moderate or greater
• Mitral or aortic valve stenosis greater than mild (ie, aortic stenosis: jet >3.0 meters per second [m/s], mean gradient >25 millimeters of mercury [mmHg], and aortic valve area <1.5 centimeters squared [cm^2]; mitral stenosis: mean gradient >5 mmHg and mitral valve area <1.5 cm^2)
• Systolic pulmonary artery pressure (SPAP) >40 mmHg (and/or tricuspid regurgitation [TR] jet velocity >2.9 m/s) In cases where an actual SPAP value is not measurable due to lack of adequate TR jet, the pulmonary flow acceleration time measured at the right ventricular outflow tract (RVOTAT) will be used to assess eligibility. Participants with a RVOTAT ≤100 milliseconds (msec) will be excluded, suggesting an elevated mean SPAP; eligibility for the those participants with RVOTAT between 100 and 120 msec will be determined based on combined assessment of the TR jet, septal motion, and right ventricular size.
• Left ventricular ejection fraction <45%
• Intracardiac mass, tumor, or thrombus
• Evidence of congenital heart disease
• Clinically significant pericardial effusion (eg, moderate or larger or with hemodynamic compromise)
• Significant renal or hepatic disease as evidenced by a serum creatinine greater than 1.5× upper limit of normal (ULN), serum transaminases greater than 3× ULN, or total bilirubin greater than 1.5× ULN in absence of Gilbert's syndrome
• Any suicidal ideation with intent with or without a plan, at the time of or within 6 months of Screening, as indicated by answering "Yes" to questions 4 or 5 on the Suicidal Ideation section of the Columbia-Suicide Severity Rating Scale (C-SSRS)
• Any suicidal behavior in the past based on the C-SSRS
• Any history of anorexia or bulimia within 2 years before Screening, Attention Deficit Hyperactivity Disorder, any Diagnostic and Statistical Manual of Mental Disorders, 5th Edition depressive disorder, bipolar disorder, or schizophrenia
• Known secondary causes (genetic, endocrine, or metabolic) for obesity (eg, Prader-Willi syndrome, Bardet Biedl syndrome, Down's Syndrome, untreated hypothyroidism, Cushing's syndrome, daily systemic corticosteroid exposure for longer than 30 days, history of significant exposure to corticosteroids for chronic illness during the past year; inhaled steroids will be allowed)
• Use of other products intended for weight loss including prescription drugs, over-the-counter (OTC) drugs, and herbal preparations within 1 month before Screening
• Use of any of the following medications:

• Serotonergic drugs within 7 days (or 5 half-lives, whichever is longer) or monoamine oxidase inhibitors within 30 days before Randomization, including:

• selective serotonin reuptake inhibitors
• serotonin norepinephrine reuptake inhibitors
• tricyclic antidepressants
• bupropion
• triptans
• St. John's Wort
• tryptophan
• linezolid
• dextromethorphan in any form (eg, OTC cold medicines)
• lithium
• tramadol
• antipsychotics or other dopamine antagonists
• Others

• antiseizure medications including valproic acid, zonisamide, topiramate, and lamotrigine
• oral steroids (topical and inhaled steroids are acceptable)
• stimulant medications (eg, Ritalin, Concerta, Biphetamine, and Dexedrine)
• benzodiazepines
• Use of drugs known to increase the risk for cardiac valvulopathy within 6 months before Screening, including but not limited to pergolide, ergotamine, methysergide, and cabergoline
• History or evidence of clinically significant disease (eg, malignancy; cardiac, respiratory, gastrointestinal, renal, or psychiatric disease) other than prediabetes (impaired fasting glucose or impaired glucose tolerance), type 2 diabetes treated with oral anti-diabetic agents (excluding sulfonylurea) or non-insulin injectable antidiabetic agents, obstructive sleep apnea, dyslipidemia, and nonalcoholic fatty liver disease
• Use of Belviq XR within 6 months before Screening or hypersensitivity to Belviq XR or any of the excipients
• Significant change in diet or level of physical activity within 1 month before dosing or change in weight of more than 5 kg within 3 months before Screening
• Any use of a very-low-calorie (<1000 calories/day) weight loss diet within 6 months before Screening
• History of alcohol or drug dependence or abuse
• Recreational drug use within 2 years before Screening
• Known to be human immunodeficiency virus positive
• Known to have active viral hepatitis (B or C)
• Malignancy within 5 years before Screening
• Unable to attend scheduled visits (eg, lack of transportation) or lack of a caregiver or guardian to supervise study participation
• Special needs participants who are unable to comprehend study-related instructions (eg, mild to profound mental retardation [intelligence quotient <70], moderate to severe cognitive developmental delay, pervasive development disorders, autism)
• Ongoing epilepsy or other seizure disorder, or use of medications for a seizure disorder within 6 months of screening or any time between screening and randomization
• Participants with a blood pressure in the 95th percentile or greater for age, sex, and height on 2 separate readings recorded on 2 separate days. Those participants who had uncontrolled hypertension at Screening can be rescreened more than 1 month after initiation or adjustment of antihypertensive therapy 1 time.
• Currently enrolled in another clinical study or has used any investigational drug or device within 30 days before providing informed consent
• Planned bariatric surgery during the study or prior bariatric surgical procedures
• Not suitable to participate in the study in the opinion of the investigator, including consideration of any existing physical, medical, or mental condition that prevents compliance with the protocol
• Female participants who are breastfeeding or pregnant at Screening or Baseline (as documented by a positive β-human chorionic gonadotropin test). A separate Baseline assessment is required if a negative screening pregnancy test was obtained more than 72 hours before the first dose of study drug.
• Female participants of childbearing potential who:

• Had unprotected sexual intercourse within 30 days before study entry and who do not agree to use a highly effective method of contraception (eg, total abstinence, an intrauterine device, a double-barrier method [such as condom plus diaphragm with spermicide], a contraceptive implant, an oral contraceptive, or have a vasectomized partner with confirmed azoospermia) throughout the entire study period and for 28 days after study drug discontinuation
• Are currently abstinent and do not agree to use a double-barrier method (as described above) or refrain from sexual activity during the study period and for 28 days after study drug discontinuation
• Are using hormonal contraceptives, but are not on a stable dose of the same hormonal contraceptive product for at least 4 weeks before dosing and who do not agree to use the same contraceptive during the study and for 28 days after study drug discontinuation (Note: All female participants will be considered to be of childbearing potential unless they have been sterilized surgically [ie, bilateral tubal ligation, total hysterectomy, or bilateral oophorectomy, all with surgery at least 1 month before dosing]).

• Minimum Eligible Age: 12 Years
• Maximum Eligible Age: 17 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Eisai Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Phoenix Clinical LLC

Phoenix, Arizona, United States

Alliance Research Institute

Bell Gardens, California, United States

Long Beach Clinical Trial Services, Inc

Long Beach, California, United States

International Research Partners LLC

Doral, Florida, United States

Oviedo Medical Research, LLC

Oviedo, Florida, United States

Gwinnett Research Institute

Buford, Georgia, United States

Columbus Regional Research Institute

Columbus, Georgia, United States

Buynak Clinical Research, PC

Valparaiso, Indiana, United States

Heartland Research Associates, LLC

Wichita, Kansas, United States

The Center for Pharmaceutical Research, LLC

Kansas City, Missouri, United States

Wake Research-Clinical Research Center of Nevada, LLC

Henderson, Nevada, United States

Diabetes & Endocrinology Consultants, PC

Morehead City, North Carolina, United States

Neuro-Behavioral Clinical Research, Inc

North Canton, Ohio, United States

Celia Reyes-Acuna, MD

Corpus Christi, Texas, United States

DCT-McAllen Primary Care, LLC dba Discovery Clinical Trials

McAllen, Texas, United States

National Clinical Research-Richmond, Inc

Richmond, Virginia, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

APD356-A001-403

Identifier Type: -

Identifier Source: org_study_id