Opiate Dependence
Conditions
Keywords
Opiate Dependence
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.
Interventions
DRUGMedisorb naltrexone 75 mg
Single administration via intramuscular (IM) injection.
DRUGMedisorb naltrexone 150 mg
Single administration via IM injection.
DRUGMedisorb naltrexone 300 mg
Single administration via IM injection.
DRUGHydromorphone (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.
DRUGNaloxone 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.
Sponsors
Alkermes, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
Primary 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 Primary
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Slope Change From Baseline for Pupil Size | 4 weeks (Baseline to Day 28) | Photographs of subjects' pupils were measured horizontally and vertically, 15 minutes before the first hydromorphone dose and every 15 minutes after each hydromorphone/placebo for hydromorphone dose, for up to 1 hour. Size was the product of vertical and horizontal measures. The slope, determined by linear regression, was used as a summary measure of the dose-response relationship between the hydromorphone dose and pupil size. The steeper the slope, the greater the hydromorphone effect. A slope of zero indicated no evidence of a hydromorphone effect. |
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Medisorb Naltrexone 75 mg Administered as a single gluteal intramuscular (IM) injection | 9 |
| Medisorb Naltrexone 150 mg Administered as a single gluteal IM injection | 8 |
| Medisorb Naltrexone 300 mg Administered as a single gluteal IM injection | 10 |
| Total | 27 |
Baseline characteristics
| Characteristic | Medisorb Naltrexone 150 mg | Medisorb Naltrexone 300 mg | Medisorb Naltrexone 75 mg | Total |
|---|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 8 Participants | 10 Participants | 9 Participants | 27 Participants |
| Age, Continuous | 42.88 years STANDARD_DEVIATION 4.7 | 32.5 years STANDARD_DEVIATION 8.02 | 35.22 years STANDARD_DEVIATION 9.28 | 36.48 years STANDARD_DEVIATION 8.6 |
| Gender Female | 0 Participants | 2 Participants | 1 Participants | 3 Participants |
| Gender Male | 8 Participants | 8 Participants | 8 Participants | 24 Participants |
| Region of Enrollment United States | 8 participants | 10 participants | 9 participants | 27 participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk |
|---|---|---|---|
| deaths Total, all-cause mortality | — / — | — / — | — / — |
| other Total, other adverse events | 6 / 9 | 5 / 8 | 7 / 10 |
| serious Total, serious adverse events | 0 / 9 | 0 / 8 | 0 / 10 |
Outcome results
Primary
Slope Change From Baseline for Pupil Size
Photographs of subjects' pupils were measured horizontally and vertically, 15 minutes before the first hydromorphone dose and every 15 minutes after each hydromorphone/placebo for hydromorphone dose, for up to 1 hour. Size was the product of vertical and horizontal measures. The slope, determined by linear regression, was used as a summary measure of the dose-response relationship between the hydromorphone dose and pupil size. The steeper the slope, the greater the hydromorphone effect. A slope of zero indicated no evidence of a hydromorphone effect.
Time frame: 4 weeks (Baseline to Day 28)
Population: Placebo hydromorphone challenge sessions were excluded from the analysis. Results for subjects who discontinued prior to Day 28 were not imputed.
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Medisorb Naltrexone 75 mg | Slope Change From Baseline for Pupil Size | -0.5540 cm(2)/hr | Standard Deviation 0.3473 |
| Medisorb Naltrexone 150 mg | Slope Change From Baseline for Pupil Size | -0.3607 cm(2)/hr | Standard Deviation 0.3998 |
| Medisorb Naltrexone 300 mg | Slope Change From Baseline for Pupil Size | -0.1410 cm(2)/hr | Standard Deviation 0.1745 |