ALK21-004: Single-dose Opiate Challenge of Medisorb® Naltrexone (VIVITROL®) in Adults Who Use Opioids

NCT ID: NCT01218984

Last Updated: 2017-01-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 27 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-03-31
• Study Completion Date: 2003-05-31

Brief Summary

This was a Phase 2, multicenter, randomized, double-blind pilot study in opioid-using adults to assess the presence, duration, and degree of opiate blockade as well as the safety and tolerability of Medisorb® naltrexone (VIVITROL®). Subjects were randomized in a 1:1:1 ratio to receive a single gluteal intramuscular (IM) injection of Medisorb naltrexone 75, 150, or 300 mg.

Detailed Description

Potential subjects were screened within 21 days prior to dosing of study drug (Medisorb naltrexone or placebo) on Day 0. Screening evaluations included a baseline hydromorphone challenge session in which increasing doses of hydromorphone (0 mg [placebo], 3 mg, 4.5 mg, and 6 mg) were administered at hourly intervals to produce a cumulative dose-response curve. Throughout the 4-hour challenge period, subject-rated measures (Visual Analog Scale [VAS] questions) and physiological measures (ie, pupil size) were recorded.

As a safety measure, at least 7 days after the baseline hydromorphone challenge, a naloxone challenge was performed followed by a 1-day oral naltrexone tolerability assessment. On Day 0, eligible subjects were administered a single dose of study drug. To assess the level of opiate blockade and surmountability attributable to Medisorb naltrexone, experimental hydromorphone challenge sessions were conducted postdose at Days 7, 14, 21, 28, 42, and 56, with a single placebo hydromorphone challenge administered at a randomly selected visit. Pupil size was measured 15 minutes prior to the first hydromorphone dose and at 15, 30, 45, and minutes after each ascending hydromorphone/placebo for hydromorphone dose. Blood samples for measurement of naltrexone and 6B-naltrexol were obtained at screening and before hydromorphone/placebo administration on Days 7, 14, 21, 28, 42, and 56.

Subjects were monitored for safety through Day 56.

Conditions

Opiate Dependence

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Medisorb naltrexone 75 mg

Group Type: EXPERIMENTAL

Medisorb naltrexone 75 mg

Intervention Type: DRUG

Single administration via intramuscular (IM) injection.

Hydromorphone (10 mg/mL)

Intervention Type: DRUG

Increasing doses of 0, 3, 4.5, and 6 mg were administered at baseline (pre-study drug administration). After study drug administration, additional hydromorphone challenge sessions consisting of administering 0, 3, 4.5, and 6 mg were administered at 1-hr intervals at each of the postdose evaluation visits. In addition, at a randomly selected evaluation visit, subjects received four 0 mg (placebo) doses at 1-hour intervals.

Naloxone Challenge and Oral Naltrexone Tolerability Testing

Intervention Type: DRUG

Administered according to the instructions provided by the respective manufacturer. Testing occurred at least 7 days after the baseline hydromorphone challenge and prior to study drug administration.

Medisorb naltrexone 150 mg

Group Type: EXPERIMENTAL

Medisorb naltrexone 150 mg

Intervention Type: DRUG

Single administration via IM injection.

Hydromorphone (10 mg/mL)

Intervention Type: DRUG

Increasing doses of 0, 3, 4.5, and 6 mg were administered at baseline (pre-study drug administration). After study drug administration, additional hydromorphone challenge sessions consisting of administering 0, 3, 4.5, and 6 mg were administered at 1-hr intervals at each of the postdose evaluation visits. In addition, at a randomly selected evaluation visit, subjects received four 0 mg (placebo) doses at 1-hour intervals.

Naloxone Challenge and Oral Naltrexone Tolerability Testing

Intervention Type: DRUG

Administered according to the instructions provided by the respective manufacturer. Testing occurred at least 7 days after the baseline hydromorphone challenge and prior to study drug administration.

Medisorb naltrexone 300 mg

Group Type: EXPERIMENTAL

Medisorb naltrexone 300 mg

Intervention Type: DRUG

Single administration via IM injection.

Hydromorphone (10 mg/mL)

Intervention Type: DRUG

Increasing doses of 0, 3, 4.5, and 6 mg were administered at baseline (pre-study drug administration). After study drug administration, additional hydromorphone challenge sessions consisting of administering 0, 3, 4.5, and 6 mg were administered at 1-hr intervals at each of the postdose evaluation visits. In addition, at a randomly selected evaluation visit, subjects received four 0 mg (placebo) doses at 1-hour intervals.

Naloxone Challenge and Oral Naltrexone Tolerability Testing

Intervention Type: DRUG

Administered according to the instructions provided by the respective manufacturer. Testing occurred at least 7 days after the baseline hydromorphone challenge and prior to study drug administration.

Interventions

Medisorb naltrexone 75 mg

Single administration via intramuscular (IM) injection.

Intervention Type: DRUG

Medisorb naltrexone 150 mg

Single administration via IM injection.

Intervention Type: DRUG

Medisorb naltrexone 300 mg

Single administration via IM injection.

Intervention Type: DRUG

Hydromorphone (10 mg/mL)

Increasing doses of 0, 3, 4.5, and 6 mg were administered at baseline (pre-study drug administration). After study drug administration, additional hydromorphone challenge sessions consisting of administering 0, 3, 4.5, and 6 mg were administered at 1-hr intervals at each of the postdose evaluation visits. In addition, at a randomly selected evaluation visit, subjects received four 0 mg (placebo) doses at 1-hour intervals.

Intervention Type: DRUG

Naloxone Challenge and Oral Naltrexone Tolerability Testing

Administered according to the instructions provided by the respective manufacturer. Testing occurred at least 7 days after the baseline hydromorphone challenge and prior to study drug administration.

Intervention Type: DRUG

Other Intervention Names

Naltrexone for extended-release injectable suspension; Naltrexone for extended-release injectable suspension; Naltrexone for extended-release injectable suspension; Dilaudid-HP®; opioid agonist; Narcan® (naloxone); ReVia® (oral naltrexone)

Eligibility Criteria

Inclusion Criteria

• Adults who had used opioids: non-medically for at least 1 year; at least once per week for at least some period during their use history; and fewer than 3 times per week on average for the 30 days prior to screening.
• Provided written informed consent
• Demonstrated a positive response to hydromorphone challenge during screening
• Willing to use contraception for study duration if of childbearing potential

Exclusion Criteria

• Any clinically significant medical condition or laboratory abnormality at screening
• Participated in a clinical trial within prior 30 days
• Dependent on opioids
• Seeking treatment for opioid abuse
• Psychosis or any major mood or anxiety disorder
• Pregnancy or lactation

• Minimum Eligible Age: 21 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Alkermes, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Alkermes, Inc.

Principal Investigators

Bernard L. Silverman, MD

Role: STUDY_DIRECTOR

Alkermes, Inc.

References

Bigelow GE, Preston KL, Schmittner J, Dong Q, Gastfriend DR. Opioid challenge evaluation of blockade by extended-release naltrexone in opioid-abusing adults: dose-effects and time-course. Drug Alcohol Depend. 2012 Jun 1;123(1-3):57-65. doi: 10.1016/j.drugalcdep.2011.10.018. Epub 2011 Nov 12.

Reference Type: RESULT

PMID: 22079773 (View on PubMed)

Other Identifiers

ALK21-004

Identifier Type: -

Identifier Source: org_study_id