Efficacy and Safety Study of Combination Therapy to Treat Uncomplicated Obesity

Phase 2, Multicenter, Randomized, Double Blind, Placebo Controlled Study of Combination Therapy for Safety and Efficacy in Subjects With Uncomplicated Obesity

Patrocinadores

Patrocinador principal: Orexigen Therapeutics, Inc

Fuente Orexigen Therapeutics, Inc
Resumen breve

The purpose of this study is to determine the efficacy and safety of 3 combinations of naltrexone and bupropion SR compared to naltrexone alone, bupropion SR alone or placebo.

Descripción detallada

A completed proof of concept study, OT-101 (Data on File, Orexigen Therapeutics, 2005), demonstrated that a combination of 300 mg bupropion SR and 50 mg naltrexone was associated with greater weight loss than bupropion SR alone, naltrexone alone, or placebo in subjects with uncomplicated obesity.

The hypothesis for the current trial is that by adjusting the doses and titration schedules of bupropion SR and naltrexone greater efficacy and improved tolerability can be achieved. In this trial, a higher dose of bupropion and 2 lower doses of naltrexone than utilized in the previous trial (OT-101) will be evaluated. The doses of both drugs will be titrated over 4 weeks and administered twice a day. There are 2 cohorts. At each site, cohort 2 recruitment began as soon as cohort 1 enrollment was completed. Cohort 1 treatment groups are (60 per group):

- Group 1: Bupropion SR (400 mg/day) plus Naltrexone (48 mg/day)

- Group 2: Bupropion SR (400 mg/day) plus Naltrexone (16 mg/day)

- Group 3: Bupropion SR (400 mg/day) plus N-Placebo

- Group 4: B-placebo plus Naltrexone (48 mg/day)

- Group 5: B-Placebo plus N-Placebo

Cohort treatment 2 Groups are:

- Group 6: B-Placebo plus N-Placebo (n=20)

- Group 7: Bupropion SR (400 mg/day) plus Naltrexone (32 mg/day)(n=60)

Estado general Completed
Fecha de inicio April 2005
Fecha de Terminación March 2007
Fecha de finalización primaria March 2007
Fase Phase 2
Tipo de estudio Interventional
Resultado primario
Medida Periodo de tiempo
Percentage change in total body weight baseline to week 24
Inscripción 410
Condición
Intervención

Tipo de intervención: Drug

Nombre de intervención: naltrexone and bupropion SR

Descripción: naltrexone 16, 32 or 48 mg/day and bupropion SR 400 mg/day

Elegibilidad

Criterios:

Inclusion Criteria:

- Female and male subjects, 18 to 60 years of age

- Have body mass index (BMI) of 30 to 40 kg/m2

- Free from clinically significant illness or disease as determined by medical history and physical examination

- Non-smoker and no use of tobacco or nicotine products for at least 6 months prior to baseline

- Normotensive (systolic <140 mm Hg; diastolic <90 mm Hg). Anti-hypertensive medications are allowed with the exception of adrenergic blockers, beta-blockers and clonidine. Medical regimen must be stable for at least 6 weeks

- LDL cholesterol < 190 mg/dL and triglycerides < 400 mg/dL. Medications for treatment of dyslipidemia are allowed as long as medical regimen has been stable for at least 6 weeks

- No clinically significant abnormality of serum albumin, blood urea nitrogen, creatinine, calcium and phosphorus

- Bilirubin, ALT and AST within 1.5 x ULN

- No clinically significant abnormality of hematocrit, white blood cell count, white cell differential, or platelets

- Fasting glucose less than 140 mg/dL on no hypoglycemic agents

- No clinically significant abnormality on urinalysis

- TSH within 1.5 x ULN, normal T3, if TSH below lower limit of normal

- Negative serum pregnancy test in women with intact uterus

- Score < 11 for depression and score < 11 for anxiety on Hospital Anxiety and Depression (HAD) Scale

- ECG: no clinically significant abnormality

- Score of zero on the Mood Assessment questionnaire and a response of "No" to the Bipolar Disorder Questions

- If female with child-bearing potential, must be non-lactating and agree to use effective contraception throughout the study period and 30 days after discontinuation of study drugs

- Able to comply with all required study procedures and schedule

- Willing and able to give written informed consent

Exclusion Criteria:

- Obesity of known endocrine origin (e.g., untreated hypothyroidism, Cushing's syndrome)

- Serious medical condition or medical condition that limits participation in the prescribed exercise program: (e.g. unstable cardiovascular disease including congestive heart failure, angina pectoris, and myocardial infarction; stroke; claudication; acute limb ischemia; acute renal or hepatic disorder; renal, hepatic or respiratory insufficiency)

- Active malignancy or history of malignancy (other than non-melanoma skin cancer or surgically cured cervical cancer) within 5 years of enrollment

- Serious psychiatric condition (e.g., any history of bipolar disorder, psychosis, suicidal attempt or post-partum depression; a history of major depression, suicidal ideation or antidepressant use within 1 year)

- Type I or Type II diabetes mellitus requiring pharmacotherapy

- Excluded concomitant medications: anorectic agents; weight loss agents; dietary supplements to promote muscle building, enhance mood, or reduce appetite; adrenergic blockers; beta blockers; anti-psychotic agents; clonidine; theophylline; cimetidine; oral corticosteroids; anti-depressant; topiramate; Depo-Provera®, smoking cessation agents; frequent, known use of opioid or opioid-like analgesics

- History of surgical intervention for obesity

- History of seizure disorder or predisposition to seizures (e.g., history of cerebrovascular accident, significant head trauma, brain surgery, skull fracture, subdural hematoma, or febrile seizures)

- History of bulimia or anorexia nervosa

- History of drug or alcohol abuse within 5 years

- History of treatment with bupropion, or naltrexone within 12 months

- History of hypersensitivity to bupropion, or naltrexone

- Use of drugs, herbs, or dietary supplements known to significantly affect body weight within one month of baseline

- Use of investigational drug, device or procedure within 90 days

- Participation in any previous clinical trial conducted by Orexigen Therapeutics

- Any condition which in the opinion of the investigator makes the subject unsuitable for inclusion in this study

Género: All

Edad mínima: 18 Years

Edad máxima: 60 Years

Voluntarios Saludables: No

Oficial general
Apellido Papel Afiliación
Frank Greenway, MD Principal Investigator Pennington Biomedical Research Center
Ubicación
Instalaciones:
Scripps Clinic Del mar | San Diego, California, 92130, United States
CSRA Partners in Health, Inc | Augusta, Georgia, 30909, United States
UK Clinical Research Organization | Lexington, Kentucky, 40536, United States
Pennington Biomedical Research Center | Baton Rouge, Louisiana, 70808, United States
Center for Nutrition and Preventive Medicine | Charlotte, North Carolina, 28211, United States
Duke University Medical Center | Durham, North Carolina, 27710, United States
MUSC Weight Management Center | Charleston, South Carolina, 29425, United States
Ubicacion Paises

United States

Fecha de verificación

April 2008

Fiesta responsable

Nombre Titulo: Eduardo Dunayevich, MD

Organización: Orexigen Therapeutics, Inc

Palabras clave
Tiene acceso ampliado No
Condición Examinar
Número de brazos 7
Grupo de brazo

Etiqueta: 1

Tipo: Experimental

Descripción: Bupropion SR (400 mg/day) plus Naltrexone (48 mg/day)

Etiqueta: 2

Tipo: Experimental

Descripción: Bupropion SR (400 mg/day) plus Naltrexone (16 mg/day)

Etiqueta: 3

Tipo: Active Comparator

Descripción: Bupropion SR (400 mg/day)

Etiqueta: 4

Tipo: Active Comparator

Descripción: Naltrexone (48 mg/day)

Etiqueta: 5

Tipo: Placebo Comparator

Descripción: B-Placebo plus N-Placebo

Etiqueta: 6

Tipo: Placebo Comparator

Descripción: B-Placebo plus N-Placebo

Etiqueta: 7

Tipo: Experimental

Descripción: Bupropion SR (400 mg/day) plus Naltrexone (32 mg/day)

Información de diseño del estudio

Asignación: Randomized

Modelo de intervención: Parallel Assignment

Propósito primario: Treatment

Enmascaramiento: Triple (Participant, Investigator, Outcomes Assessor)

Fuente: ClinicalTrials.gov