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Naltrexone for Antipsychotic-Induced Weight Gain

Naltrexone for Antipsychotic-Induced Weight Gain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01866098
Acronym
NTX
Enrollment
144
Registered
2013-05-31
Start date
2013-05-31
Completion date
2019-04-07
Last updated
2021-10-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bipolar Disorder, Schizoaffective Disorder, Schizophrenia, Schizophreniform Disorder, Severe Major Depression With Psychotic Features

Keywords

antipsychotic, severe mental illness, weight loss

Brief summary

This study is designed to look at the effects of naltrexone on weight loss in individuals treated with antipsychotic medications. Naltrexone is an FDA approved medication for the management of alcohol dependence and drug dependence, but has not been fully evaluated for its effect on weight loss in individuals with severe mental illness (i.e. schizophrenia, schizoaffective disorder, bipolar disorder etc.) The purpose of this study is to find out how effective two different doses of oral naltrexone is on reducing body weight when compared to placebo (an inactive substance or sugar pill).

Detailed description

Persons with severe mental illness (SMI) die, on average, 25 years earlier than the general population1. Most of this early mortality can be attributed to cardiovascular disease (CVD) and diabetes mellitus (DM), which are directly related to obesity. Obesity is a leading cause of preventable death in the United States, second only to smoking. The physical health of patients has become a major focus of schizophrenia care, as recent decades have seen immense gains in symptom control and community integration. There is an urgent need for the development of interventions that address the obesity crisis in schizophrenia. Patients treated with antipsychotic medications have been shown to have a preference for diets high in fat and sugar. Patients with schizophrenia typically seek behaviors that increase dopamine mediated reward in the brain such as smoking and substance use, both of which occur more often in this group than the general population. The system might require intact dopamine and opioid function. Naltrexone is an oral agent that competitively antagonizes all known opioid receptors in the brain. Human studies with naltrexone were completed in individuals with different illnesses, including schizophrenia, and have been shown to be a safe and easy agent to use. It is shown to decrease craving in alcoholics and is approved by the FDA for the treatment of alcohol dependence. Naltrexone is reported to decrease craving for other substances of abuse, like nicotine. Furthermore, it has been shown to prevent secondary weight gain due to cessation of cigarette smoking at low (25mg and 50 mg), but not higher doses. Naltrexone has been tested in human feeding studies, and has been shown to reduce both the quantity of food eaten and the choice of palatable foods. Subjects will be randomized to either 25, 50 or 0mg of Naltrexone and will take the study medication daily for 52 weeks. Subjects will be seen weekly for the first 4 weeks of the study, thereafter they will be seen on a bi-weekly (every other week) basis to be assessed (i.e. weight, side effect check, paper questionnaires) throughout the remaining 48 weeks of treatment. The purpose of this study is to determine the efficacy of two doses of naltrexone (25mg & 50mg) versus placebo for weight and health risk reduction in 144 obese individuals with severe mental illness treated with an antipsychotic medication.

Interventions

DRUGNaltrexone

25 or 50mg (randomized) oral capsule taken once daily for 52 weeks to establish optimal dose for weight loss over the course of the study.

DRUGPlacebo

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
Yale University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 18 to 75 * Meet Diagnostic & Statistical Manual - 4 (DSM-IV) criteria for schizophrenia, schizoaffective disorder, bipolar disorder, major depression, or another psychotic disorder based on Structured Clinical Interview for the DSM-IV (SCID) interview * Body Mass Index (BMI) of 28 and over * On a stable dose of antipsychotic medication; i.e. at least one month with no dose change, and three months from an antipsychotic switch * Deemed to be symptomatically stable by the clinical staff in the last two months * Over 7% total body weight increase on antipsychotics for subjects within first year of illness

Exclusion criteria

* Meet criteria for current opiate abuse or dependence (confirmed by positive urine drug screen for opiates or, if suspected by study doctor via patient history and or suspicion of occult opiate use, a naloxone challenge will be performed.) * Current history of dementia, mental retardation * Not capable of giving informed consent for participation in the study * Women who are pregnant or breast-feeding * Physical conditions affecting body weight (e.g. Cushing's disease, polycystic ovary syndrome) Diabetes Mellitus (defined as prescribed an anti-diabetic medication for diabetes or a hemoglobin A1c level \> 7 confirmed by primary care physician at screening) * Severe liver dysfunction, (serum aminotransferases greater than three times normal), acute infectious hepatitis, liver failure.

Design outcomes

Primary

MeasureTime frameDescription
Change in Weight From BaselineBaseline and 52 weeksWeight (kilograms; kg) will be measured at each assessment and change in weight will be determined at study endpoint.
Percent of Subjects Who Lost More Than 5% of Body Weight From Baseline52 weeksBody Mass Index will be calculated at each assessment and change over time will be assessed at endpoint.

Secondary

MeasureTime frameDescription
Changes in Insulin From BaselineBaseline and 52 weeksInsulin will be collected over the course of participation and changes will be evaluated at study endpoint.
Changes in Total Cholesterol From BaselineBaseline and 52 weeksTotal Cholesterol will be collected over the course of participation and changes will be evaluated at study endpoint.
Changes in Fasting Glucose From BaselineBaseline and 52 weeksFasting glucose will be collected over the course of participation and changes will be evaluated at study endpoint.
Changes in LDL From BaselineBaseline and 52 weeksLow-density lipoprotein (HDL) will be collected over the course of participation and changes will be evaluated at study endpoint.
Changes in HDL From BaselineBaseline and 52 weeksHigh-density lipoprotein (HDL) will be collected over the course of participation and changes will be evaluated at study endpoint.
Changes in Glycosylated Hemoglobin (HbA1c) From BaselineBaseline and 52 weeksGlycosylated hemoglobin (HbA1c) will be collected over the course of participation and changes will be evaluated at study endpoint.

Countries

United States

Participant flow

Participants by arm

ArmCount
Placebo
Oral placebo capsule taken once daily for 52 weeks Placebo
51
Naltrexone 25mg
Oral Naltrexone 25mg capsule taken once daily for 52 weeks Naltrexone: 25 or 50mg (randomized) oral capsule taken once daily for 52 weeks to establish optimal dose for weight loss over the course of the study.
47
Naltrexone 50mg
Oral Naltrexone 50mg capsule taken once daily for 52 weeks Naltrexone: 25 or 50mg (randomized) oral capsule taken once daily for 52 weeks to establish optimal dose for weight loss over the course of the study.
46
Total144

Withdrawals & dropouts

PeriodReasonFG000FG001FG002
Overall StudyAdverse Event154
Overall StudyDeath010
Overall StudyLost to Follow-up111813
Overall StudyNon-compliance101
Overall StudyPhysician Decision012
Overall StudyPregnancy200
Overall StudyProtocol Violation100
Overall StudyUnrelated Hospitalization201
Overall StudyWithdrawal by Subject120

Baseline characteristics

CharacteristicPlaceboNaltrexone 25mgNaltrexone 50mgTotal
Age, Continuous42.8 years
STANDARD_DEVIATION 12.8
45.0 years
STANDARD_DEVIATION 11.5
43.0 years
STANDARD_DEVIATION 14.2
43.6 years
STANDARD_DEVIATION 12.8
Body Mass Index (BMI)39.1 weight in kg/ height m^2
STANDARD_DEVIATION 7.3
37.1 weight in kg/ height m^2
STANDARD_DEVIATION 5.7
38.9 weight in kg/ height m^2
STANDARD_DEVIATION 11.4
38.4 weight in kg/ height m^2
STANDARD_DEVIATION 8.4
Race/Ethnicity, Customized
African American
24 Participants28 Participants16 Participants68 Participants
Race/Ethnicity, Customized
Other
9 Participants3 Participants3 Participants15 Participants
Race/Ethnicity, Customized
White/Caucasian
18 Participants16 Participants27 Participants61 Participants
Region of Enrollment
United States
51 participants47 participants46 participants144 participants
Sex: Female, Male
Female
30 Participants22 Participants25 Participants77 Participants
Sex: Female, Male
Male
21 Participants25 Participants21 Participants67 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 511 / 470 / 46
other
Total, other adverse events
35 / 5133 / 4735 / 46
serious
Total, serious adverse events
0 / 511 / 470 / 46

Outcome results

Primary

Change in Weight From Baseline

Weight (kilograms; kg) will be measured at each assessment and change in weight will be determined at study endpoint.

Time frame: Baseline and 52 weeks

Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChange in Weight From Baseline-0.16 kgStandard Error 1.78
Naltrexone 25mgChange in Weight From Baseline0.69 kgStandard Error 2.22
Naltrexone 50mgChange in Weight From Baseline-0.95 kgStandard Error 2.06
p-value: 0.83Mixed Models Analysis
Primary

Percent of Subjects Who Lost More Than 5% of Body Weight From Baseline

Body Mass Index will be calculated at each assessment and change over time will be assessed at endpoint.

Time frame: 52 weeks

Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
PlaceboPercent of Subjects Who Lost More Than 5% of Body Weight From Baseline10 Participants
Naltrexone 25mgPercent of Subjects Who Lost More Than 5% of Body Weight From Baseline4 Participants
Naltrexone 50mgPercent of Subjects Who Lost More Than 5% of Body Weight From Baseline9 Participants
p-value: 0.1Chi-squared
Secondary

Changes in Fasting Glucose From Baseline

Fasting glucose will be collected over the course of participation and changes will be evaluated at study endpoint.

Time frame: Baseline and 52 weeks

Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChanges in Fasting Glucose From Baseline8.2 mg/dLStandard Error 2.6
Naltrexone 25mgChanges in Fasting Glucose From Baseline4.6 mg/dLStandard Error 3.2
Naltrexone 50mgChanges in Fasting Glucose From Baseline-0.4 mg/dLStandard Error 2.9
p-value: 0.19Mixed Models Analysis
Secondary

Changes in Glycosylated Hemoglobin (HbA1c) From Baseline

Glycosylated hemoglobin (HbA1c) will be collected over the course of participation and changes will be evaluated at study endpoint.

Time frame: Baseline and 52 weeks

Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChanges in Glycosylated Hemoglobin (HbA1c) From Baseline-0.007 mg/dLStandard Error 0.11
Naltrexone 25mgChanges in Glycosylated Hemoglobin (HbA1c) From Baseline-0.061 mg/dLStandard Error 0.15
Naltrexone 50mgChanges in Glycosylated Hemoglobin (HbA1c) From Baseline0.060 mg/dLStandard Error 0.39
p-value: 0.96Mixed Models Analysis
Secondary

Changes in HDL From Baseline

High-density lipoprotein (HDL) will be collected over the course of participation and changes will be evaluated at study endpoint.

Time frame: Baseline and 52 weeks

Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChanges in HDL From Baseline0.04 mg/dLStandard Error 1.73
Naltrexone 25mgChanges in HDL From Baseline0.79 mg/dLStandard Error 2.19
Naltrexone 50mgChanges in HDL From Baseline0.36 mg/dLStandard Error 1.93
p-value: 0.95Mixed Models Analysis
Secondary

Changes in Insulin From Baseline

Insulin will be collected over the course of participation and changes will be evaluated at study endpoint.

Time frame: Baseline and 52 weeks

Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChanges in Insulin From Baseline6.45 mg/dLStandard Error 4.89
Naltrexone 25mgChanges in Insulin From Baseline0.45 mg/dLStandard Error 6.23
Naltrexone 50mgChanges in Insulin From Baseline2.16 mg/dLStandard Error 5.55
p-value: 0.92Mixed Models Analysis
Secondary

Changes in LDL From Baseline

Low-density lipoprotein (HDL) will be collected over the course of participation and changes will be evaluated at study endpoint.

Time frame: Baseline and 52 weeks

Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChanges in LDL From Baseline-10.87 mg/dLStandard Error 4.47
Naltrexone 25mgChanges in LDL From Baseline1.14 mg/dLStandard Error 5.46
Naltrexone 50mgChanges in LDL From Baseline-4.40 mg/dLStandard Error 4.91
p-value: 0.43Mixed Models Analysis
Secondary

Changes in Total Cholesterol From Baseline

Total Cholesterol will be collected over the course of participation and changes will be evaluated at study endpoint.

Time frame: Baseline and 52 weeks

Population: Analysis population consists of participants who were randomized, received at least 1 dose of the trial compound (naltrexone or placebo), and had at least 1 assessment after baseline.

ArmMeasureValue (LEAST_SQUARES_MEAN)Dispersion
PlaceboChanges in Total Cholesterol From Baseline-1.16 mg/dLStandard Error 5.12
Naltrexone 25mgChanges in Total Cholesterol From Baseline1.52 mg/dLStandard Error 6.41
Naltrexone 50mgChanges in Total Cholesterol From Baseline-3.02 mg/dLStandard Error 5.72
p-value: 0.98Mixed Models Analysis

Source: ClinicalTrials.gov · Data processed: Mar 23, 2026