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Buprenorphine/Naloxone Treatment for Opioid Dependence-Experiment II-3 - 6

University of Colorado Denver (CU Denver) logo

University of Colorado Denver (CU Denver)

Status and phase

Withdrawn
Phase 2

Conditions

Heroin Dependence
Opioid-Related Disorders

Treatments

Drug: Placebo Drug
Drug: Test Drug

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00000331
R01DA011160 (U.S. NIH Grant/Contract)
NIDA-11160-6
R01-11160-6

Details and patient eligibility

About

The purpose of this study is to assess the abuse liability and examine the reinforcing effects of intravenous buprenorphine and buprenorphine/naloxone combinations in healthy, non-drug dependent volunteers.

Full description

not available at this time

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Individuals must be healthy, non-drug dependent volunteers, be at least 18 years of age, and have no prior history of drug or alcohol abuse or dependence. Subjects must have had some minimal experience with opioids (e.g. at least two prior exposures)

Exclusion criteria

Individuals with evidence of an active Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) Axis I psychiatric disorder (e.g. psychosis, manic-depressive illness, organic psychiatric disorders), significant medical illness (e.g., liver or cardiovascular disease) or pregnant female subjects are excluded from study participation.

Trial design

0 participants in 2 patient groups, including a placebo group

Test Drug
Experimental group
Description:
Test drug to prevent heroine withdrawal
Treatment:
Drug: Test Drug
Placebo Pill
Placebo Comparator group
Description:
Placebo drug
Treatment:
Drug: Placebo Drug

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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