| Eligibility |
Inclusion Criteria:
- Willing and able to provide written informed consent
- Adult men or women aged 18 to 55 years, inclusive
- History of recreational opioid use defined as non therapeutic use at least 10 times in
the subject's lifetime and at least once in the 12 weeks prior to the Enrollment Visit
- Body mass index between 19 kg/m2 and 32 kg/m2 inclusive, with a body weight of not
less than 50 kg at Enrollment
- Subjects must be in good health as determined by medical history, physical
examination, 12 lead electrocardiogram (ECG), and vital signs (pulse rate, systolic
blood pressure and diastolic blood pressure, respiratory rate, and oxygen saturation
using pulse oximetry) at Enrollment
Exclusion Criteria:
- Exclusion Criteria for Enrollment:
- Self-reported history of drug or alcohol dependence (lifetime) other than caffeine or
nicotine as defined by DSM IV-TR criteria
- Current treatment or treatment within their lifetime for substance disorders, other
than treatment for smoking cessation
- Positive or missing alcohol breath test at Enrollment; the alcohol breath test can be
repeated and/or the subject rescheduled at the discretion of the investigator or
designee
- Pregnant or breastfeeding or missing pregnancy test
- Unwillingness or inability to abstain from recreational drug use for the duration of
the trial
- Current consumption of greater than 20 cigarettes per day or inability to abstain from
smoking (or use of any nicotine-containing substance) for at least 8 hours
- Participation in another clinical trial within 30 days prior to Enrollment that
resulted in the administration of at least 1 dose of IMP
- Diseases or conditions known to interfere with the absorption, distribution,
metabolism, or excretion of drugs. Subjects with a history of cholecystectomy are not
excluded
- Prolongation of QTcF (after repeated assessment) at Enrollment, i.e., >450 ms for men
or >470 ms for women, or presence of additional risk factors for torsade de pointes
(e.g., heart failure, hypokalemia), or use of concomitant medications that prolong the
QT interval
- History of orthostatic hypotension or other cardiovascular diseases
- Any clinically significant disease that in the investigator's opinion may affect
efficacy or safety assessments or may compromise the subject's safety during trial
participation, e.g., significant pulmonary, gastrointestinal, cardiac, endocrine,
metabolic, neurological, or psychiatric disorders
- Definite or suspected history of drug allergy or hypersensitivity to opioids or opioid
antagonists
- Use of prescription medications within the longer of 14 days or 5 half-lives or use of
over-the-counter medications within the longer of 7 days or 5 half-lives prior to
dosing, exceptions may be made on a case-by-case basis (e.g., for medications with a
short half-life or for topical medications) if approved by the medical monitor in
agreement with the investigator
- Any contraindication for naloxone, oxycodone IR, or tramadol IR administration
- Not able to abstain from consumption of beverages or food containing caffeine (tea,
coffee, cola, chocolate, etc.) or alcohol from 2 days prior to each Day 1 until
discharge from the research unit; beverages or food containing quinine (e.g., bitter
lemon, tonic water) from 1 week before Day 1 of the Qualification Phase until the
final examination; grapefruit juice (sweet or sour) or Seville oranges from 1 week
before Day 1 of the Qualification Phase until the final examination.
- Blood loss of 500 mL or more within 4 weeks before dosing in the treatment phase in
this trial, including blood donation. Planned blood donations during the trial and up
to 12 weeks after the Final Examination
- History of seizure disorder including unprovoked seizure and/or epilepsy or any
condition associated with a significant risk for seizure disorder or epilepsy at the
Enrollment Visit at the discretion of the investigator
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