Efficacy of Naltrexone HCl/Bupropion HCl Extended Release Versus Placebo for Treatment of Weight Regain in Participants Post Bariatric Surgery

Withdrawn before enrolling · Phase 4 · Has a placebo group

Conditions studied: Weight Regain Post Bariatric Surgery

In brief

The purpose of this study is to determine the effect of naltrexone hydrochloride(HCL) and bupropion hydrochloride extended release combination (NB) compared with placebo on weight loss in obese participants post bariatric surgery.

Key facts

Study ID: NCT02616315
Run by: Takeda
People needed: 0
Starts: 2016-02-01
Expected to finish: 2017-12-01
Last updated by the study team: 2016-04-08

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

In the opinion of the investigator, the participant is capable of understanding and complying with protocol requirements.
The participant signs and dates a written, informed consent form and any required privacy authorization prior to the initiation of any study procedures.
Is female or male and aged 18 to 65 years, inclusive.
Is at least 2 years post Roux-en-Y Gastric Bypass (RYGB) procedure for treatment of severe obesity prior to screening.
Has achieved an initial weight loss of ≥20% of their preoperative body weight, and has regained ≥10% of the total weight lost.
Has a body mass index (BMI) (weight [kg]/[height {m}]\^2) ≥30 kg/m\^2.
A female participant of childbearing potential who is sexually active with a nonsterilized male partner agrees to routinely use adequate contraception from signing of informed consent throughout the duration of the study and for 12 weeks after the last dose of study drug.
Is able to speak and read English.

You may not qualify if…

Has obesity of known endocrine origin (eg, untreated hypothyroidism, Cushing's syndrome) or of genetic origin.
Is currently using other bupropion- or naltrexone-containing products or has a history of hypersensitivity or allergies to naltrexone or bupropion.
Has a history of cancer that has been in remission for <5 years prior to screening. A history of basal cell carcinoma or Stage 1 squamous cell carcinoma of the skin is allowed.
Has a history of Type 1 or current type 2 diabetes mellitus (T2DM) diagnosis.
Has had a myocardial infarction within 6 months prior to screening.
Has a history of Class III or IV congestive heart failure, as per the New York Heart Association functional classification.
Has a history of angina pectoris Grade III or IV, as per the Canadian Cardiovascular Society grading scheme.
Has a clinical history of strokes, including ischemic and hemorrhagic strokes.
Has a history (within the last 20 years) of seizures, cranial trauma, active bulimia, anorexia nervosa, or other conditions that predispose the participant to seizures.
Has, in the judgment of the investigator, any clinically significant electrocardiogram (ECG), laboratory, hematology, physical examination, medical history, or urinalysis finding that should prohibit participation in the study.
Has uncontrolled hypertension defined as blood pressure (BP) ≥145/95 mm Hg at screening. BP will be measured on 2 separate occasions with an approximate 30-minute interval between measurements at the screening visit.
Has a thyrotropin (thyroid stimulating hormone -TSH) value outside the normal range at the screening visit; unless there is a normal triiodothyronine (T3) value.
Had initiation or alteration of dose of antihypertensive or lipid-lowering agents within 4 weeks prior to screening.
Used prescribed or over-the-counter drugs intended for weight loss, or participated in a weight loss program other than standard of care for a post bariatric population, within 3 months prior to randomization.
Has prior or planned surgical or device intervention for obesity except for the required RYGB Surgery.
Has a history or current diagnosis of angle-closure glaucoma.
Is experiencing post bariatric dumping syndrome that may impact the conduct or outcome of the study as determined by the investigator.
Has moderate or severe renal impairment (end-stage renal disease) defined as estimated glomerular filtration rate (eGFR) <60 mL/min/1.73m\^2, using the Chronic Kidney Disease Epidemiology Collaboration equation (CKD-EPI).
Has a clinical history of hepatic impairment or current documented aspartate aminotransferase (AST) or alanine aminotransferase (ALT) >3 times the upper limit of normal (ULN) at the screening visit.
Has glycosylated hemoglobin (HbA1c) ≥6.5% at Screening Visit.
Has current known infection with human immunodeficiency virus (HIV) or hepatitis (documentation of no detectable virus is required for participants with a past infection of hepatitis B or C).
Is undergoing an abrupt discontinuation of alcohol, benzodiazepines, barbiturates, or antiepileptic drugs.
Is a chronic user or has a positive screen for opioids.
Has a hemoglobin of ≤10 g/100 mL at the screening visit.
Has a history of serious psychiatric illness such as:

Where it is running

Study site — Chicago, Illinois, United States
Study site — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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