Buprenorphine Dose Escalation Trial for Treatment of Non-Dependent Opiate Users - 2

Substance-Related Disorders Clinical Trial

Official title:

PK 0396 - Buprenorphine Dose Escalation Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00015041
• Other study ID #: NIDA-5-0012-2
• Secondary ID: Y01-5-0012-2
• Status: Completed
• Phase: Phase 1
• First received: April 18, 2001
• Last updated: January 11, 2017
• Start date: November 1996
• Est. completion date: July 1998

Study information

• Verified date: July 1998
• Source: National Institute on Drug Abuse (NIDA)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effect, pharmacokinetics and dose proportionality of buprenorphine when administered to non-dependent opiate users. 1) To evaluate whether plasma concentrations of buprenorphine increase proportionally to buprenorphine dose. 2) To evaluate the dose-response of subjective and physiological effects of buprenorphine; and 3) To determine the safety of buprenorphine.

Description:

This will be an open-label, single dose-escalation trial. A total of 24 opiate experienced, but not dependent subjects will receive four ascending doses of buprenorphine, 4, 8, 16, and 24 mg, respectively, with an at least a 14 day washout interval between treatments. The four treatments are sublingual administration of:

1. two 2-mg buprenorphine sublingual tablets,

2. one 8-mg buprenorphine sublingual tablet,

3. two 8-mg buprenorphine sublingual tablets; and

4. three 8-mg buprenorphine sublingual tablets.

The dose proportionality in plasma profiles of buprenorphine and dose response of the buprenorphine sublingual tablets are evaluated at buprenorphine dose range of 4 to 24 mg.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Est. completion date: July 1998
• Est. primary completion date: June 1998
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years to 45 Years

Eligibility

Inclusion Criteria:

1. Be male or female of any race, between 21 and 45 years of age.

2. Weigh within 15% of ideal body weight for height according to the current life insurance table.

3. Be in good physical and mental health as judged by interview and physical examination.

4. Have no significant oral cavity pathology including excessive caries, gingivitis, infectious or inflammatory disease, or recent piercing of the oral cavity.

5. Be experienced in illicit use of opiates but not be physically dependent on opiates and other drugs (except nicotine or caffeine) at the time of the study. A history of other psychoactive drug use is acceptable but preference will be for subjects reporting less frequent and more controlled illicit drug use.

6. For female subjects, test nonpregnant and use adequate birth control, and not be lactating.

7. Be capable of providing written informed consent to participate in this study.

8. Be able to comply with protocol requirements and be likely to complete all four study treatments.

Exclusion Criteria:

1. Have a diagnosis of drug addiction (other than nicotine, caffeine, and opiate) as per DSM-IV criteria.

2. Have any significant, active medical or psychiatric illnesses (other than drug dependence) which might inhibit their ability to complete the study or might be complicated by administration of study medications.

3. Have clinically significant abnormal laboratory measurements in liver function tests (AST and ALT levels greater than 3 times the upper limit of normal), hematology (CBC, differential, platelet count), serum chemistries (SMA-24) and urinalysis at screening.

4. Test positive on the HIV blood screen.

5. Have a history of significant hepatic, renal, endocrine, cardiac, nervous, psychiatric, gastrointestinal, pulmonary, hematologic or metabolic disorders.

6. Have known hypersensitivity to buprenorphine and its derivatives or opiates or opiate-like analgesics.

7. Receive any medications for medical conditions.

8. Have any condition or history considered by the investigator(s) to place the subjects at increased risk.

9. Do not actively meet the inclusion criteria at the time of screening.

Study Design

Primary Purpose: Treatment

Related Conditions & MeSH terms

• Disease
• Opioid-Related Disorders
• Substance-Related Disorders

Intervention

Drug:
• Buprenorphine

Locations

Country	Name	City	State
United States	Cincinnati MDRU	Cincinnati	Ohio

Sponsors (2)

Lead Sponsor	Collaborator
National Institute on Drug Abuse (NIDA)	Cincinnati MDRU

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	PK parameters of buprenorphine
Primary	Intoxication and withdrawal