The Safety of Using Buprenorphine With Naloxone in a Buccal Film to Initiate Treatment of Opioid Dependent Subjects

Withdrawn before enrolling · Phase 3

Conditions studied: Opioid Dependence

In brief

A randomized, double blind, active controlled study in approximately 40 opioid dependent subjects. Study duration is up to five days and includes a maximum of 3 days confinement in the clinic. Opioid dependent subjects who provide informed consent meet all entry criteria are eligible for enrollment into the study.

Key facts

Study ID

NCT02516436

Run by

BioDelivery Sciences International

People needed

0

Expected to finish

2017-05-01

Last updated by the study team

2017-05-04

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Signed informed consent obtained prior to any study procedure being performed
• Pre-specified plan for continued treatment following study participation
• Male or non-pregnant and non-nursing female. A female of childbearing potential is eligible to participate in this study if she is not pregnant and is using an acceptable method of birth control.
• Subject is aged 18 to 55 years, inclusive
• Current diagnosis of opioid substance use disorder per the Diagnostic and Statistical Manual of Mental Disorders - 5th edition (DSM-5)
• Clinical opioid withdrawal scale (COWS) total score ≥12 prior to dosing on Day 1
• Subject is otherwise in good general health in the judgment of the Investigator as determined from the physical and oral examination findings.
• Subject is committed to getting help for their opioid dependence, in the judgment of the Investigator.
• Subject has at least 1 verified contact.

You may not qualify if…

• Inability to meet study participation requirements, including a stay of up to 2 nights in the clinic
• Positive buprenorphine or methadone result on urine drug screen at Screening or Baseline
• Concurrent Diagnostic and Statistical Manual of Mental Disorders - 5th edition diagnosis of substance use disorder (excluding opioids and tobacco)
• Prolonged QT interval by medical history, family history, or current electrocardiogram (ECG) finding
• History of clinically significant hepatic impairment as determined by the Investigator.
• Use of any medication, nutraceutical or herbal product with CYP3A4 inhibition or induction properties within the past 30 days. This exclusion also extends to grapefruit juice and grapefruit juice-containing products as well as St. John's wort and St. John's wort-containing products (prescription or nonprescription drugs, vitamins, minerals, or dietary/herbal supplements).
• Use of an investigational drug or device within the last 30 days
• History of hypersensitivity, allergy, or intolerance to buprenorphine or naloxone
• Increased suicidal risk, as determined by meeting any of the following:
• History of suicidal ideation ≤ 3 months prior to Baseline with a score of 4 (intent to act) or 5 (specific plan and intent) on the electronic Columbia Suicide Severity Rating Scale (eC-SSRS)
• History of suicidal behavior ≤1 year prior to Baseline (actual attempt, interrupted attempt, aborted attempt and/or preparatory acts/behavior) on the electronic Columbia Suicide Severity Rating Scale (eC-SSRS)
• Lack of motivation or a pattern of prior poor response to treatment, as judged by the investigator
• A history or current evidence of any clinically significant disorder or any other condition which in the opinion of the Investigator, would jeopardize the safety of the subject or impact the validity of the study results

Where it is running

• Study site — Birmingham, Alabama, United States
• Study site — Orem, Utah, United States
• Study site — Salt Lake City, Utah, United States

Full record on ClinicalTrials.gov

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