Abuse Potential of HORIZANT With and Without Oxycodone in Healthy, Nondependent Recreational Opioid Users

NCT ID: NCT06247488

Last Updated: 2024-08-12

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 110 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-01-31
• Study Completion Date: 2023-04-25

Brief Summary

The purpose of this study is to assess the abuse potential of gabapentin enacarbil immediate release capsules taken alone and in combination with oxycodone in healthy adult, non-dependent, recreational opioid users.

Detailed Description

The primary purpose of this study is to evaluate the abuse potential of gabapentin enacarbil immediate-release (GE-IR), the active moiety in Horizant, taken alone and taken in combination with oxycodone, compared to that of oxycodone alone.

This study is a randomized, double-blind, active- and placebo-controlled, 6-way crossover design, aimed to assess the abuse potential, safety, and pharmacokinetics (PK) of GE-IR doses when administered alone or in combination with an opioid active control (oxycodone), and compared to placebo and oxycodone intake alone, in healthy, nondependent, recreational opioid users.

Conditions

Abuse Potential

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: OTHER
• Blinding Strategy: QUADRUPLE

Study Groups

Placebo

oral masked Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Participant will receive oral dose of placebo.

Oxycodone 20 mg

oral active control

Group Type: ACTIVE_COMPARATOR

Oxycodone 20 mg

Intervention Type: DRUG

Participant will receive oral dose of oxycodone 20 mg.

GE-IR 200mg

single oral dose

Group Type: EXPERIMENTAL

GE-IR 200 mg

Intervention Type: DRUG

Participant will receive oral dose of GE-IR 200 mg and oxycodone 20 mg.

GE-IR 450 mg

single oral dose

Group Type: EXPERIMENTAL

GE-IR 450 mg

Intervention Type: DRUG

Participant will receive oral dose of GE-IR 450 mg and oxycodone 20 mg.

GE-IR 200 mg + Oxycodone 20 mg

oral doses given together

Group Type: EXPERIMENTAL

Oxycodone 20 mg

Intervention Type: DRUG

Participant will receive oral dose of oxycodone 20 mg.

GE-IR 200 mg

Intervention Type: DRUG

Participant will receive oral dose of GE-IR 200 mg and oxycodone 20 mg.

GE-IR 450 mg + Oxycodone 20 mg

oral doses given together

Group Type: EXPERIMENTAL

Oxycodone 20 mg

Intervention Type: DRUG

Participant will receive oral dose of oxycodone 20 mg.

GE-IR 450 mg

Intervention Type: DRUG

Participant will receive oral dose of GE-IR 450 mg and oxycodone 20 mg.

Interventions

Placebo

Participant will receive oral dose of placebo.

Intervention Type: DRUG

Oxycodone 20 mg

Participant will receive oral dose of oxycodone 20 mg.

Intervention Type: DRUG

GE-IR 200 mg

Participant will receive oral dose of GE-IR 200 mg and oxycodone 20 mg.

Intervention Type: DRUG

GE-IR 450 mg

Participant will receive oral dose of GE-IR 450 mg and oxycodone 20 mg.

Intervention Type: DRUG

Other Intervention Names

matching over-encapsulated capsule; Oxycontin; Gabapentin Enacarbil, Horizant; Gabapentin Enacarbil, Horizant

Eligibility Criteria

Inclusion Criteria

1. Provision of signed and dated informed consent form (ICF),

2. Stated willingness to comply with all study procedures and availability for the duration of the study,

3. Male or female, between 18 and 55 years of age, inclusive,

4. Current nondependent, recreational opioid user who has used opioid drugs for recreational (nontherapeutic) purposes (i.e., for psychoactive effects) at least 5 times in the subject's lifetime and at least once in the last 12 weeks,

5. Body mass index (BMI) within 18.0 kg/m2 to 36.0 kg/m2, inclusive,

6. If female, meets 1 of the following criteria:

1. If of childbearing potential agrees to use 1 of the accepted contraceptive regimens from at least 30 days prior to the first study treatment administration, during the study, and for at least 30 days after the last dose of the study treatment. An acceptable method of contraception includes 1 of the following:

• Abstinence from heterosexual intercourse,
• Hormonal contraceptives (birth control pills, injectable/implantable/insertable hormonal birth control products, transdermal patch), or
• Intrauterine device (IUD; with or without hormones). Or

2. If of childbearing potential agrees to use a double barrier method (e.g., condom and spermicide) during the study and for at least 30 days after the last dose of study treatment.

Or

3. If of non-childbearing potential, defined as surgically sterile (i.e., has undergone complete hysterectomy, bilateral oophorectomy or tubal ligation) or is in a postmenopausal state (i.e., at least 1 year without menses without an alternative medical condition and confirmed follicle stimulating hormone (FSH) ≥ 40 milli-International unit (mIU)/mL prior to the first study treatment administration),

7. If male and engaging in sexual activity that has the risk of pregnancy must agree to use a double barrier method (e.g., condom and spermicide) and agree to not donate sperm during the study and for at least 90 days after the last dose of study treatment, a male who has a pregnant partner shall be excluded,

8. Healthy, as determined by no clinically significant findings from medical history, physical examination, 12-lead ECG, vital signs or clinical laboratory (including hematology, clinical chemistry, urinalysis, and serology [screening visit only]) at screening visit and admission, in the opinion of an investigator.

9. Negative COVID-19 test prior to each admission.

Exclusion Criteria

1. History of significant hepatic, renal, cardiovascular, pulmonary, hematologic, neurological, psychiatric, gastrointestinal, endocrine, immunologic, ophthalmologic, or dermatologic disease of any etiology (including infections),

2. Presence or history of significant gastrointestinal, liver or kidney disease, or surgery that may affect drug bioavailability with the exception that cholecystectomy is permitted at the discretion of an investigator,

3. Presence of any significant respiratory illness or presence or history of chronic respiratory disease (e.g., upper respiratory illness, sleep apnea, emphysema, asthma) at screening (subjects with acute respiratory illness may be rescheduled upon resolution at the discretion of an investigator),

4. Personal or family history (first degree relatives) of allergy, hypersensitivity, or drug rash with eosinophilia and systemic symptoms (DRESS) syndrome to gabapentin enacarbil,gabapentin or any drug product including naloxone, opioids (e.g., oxycodone), or related drugs or known excipients of any of the drug products in this study (e.g. lactose),

5. History of sensitivity to or poor tolerance of gabapentin enacarbil, gabapentin, pregabalin, naloxone, or oxycodone,

6. Female who is lactating at screening,

7. Female who is pregnant according to the pregnancy test at screening or prior to the first study treatment administration or planning to become pregnant within 30 days following the last study treatment administration,

8. History of substance or alcohol dependence (excluding nicotine and caffeine) within the past 2 years, as defined by the Diagnostic and Statistical Manual of Mental Disorders, 4th Edition (DSM-IV), and/or subject has ever been in a drug or alcohol rehabilitation program within the last 2 years,

9. Subjects with positive urine drug screen (UDS) results at screening and admission will be assessed for inclusion at the discretion of an Investigator. If tetrahydrocannabinol (THC) is positive at admission to the qualification phase and treatment phase, a cannabis intoxication evaluation will be done by an investigator and subjects may be permitted to continue in the study, rescheduled, or discontinued at the discretion of an investigator. Other positive test results should be reviewed to determine if the subject may be rescheduled, in the opinion of the investigator,

10. Is a heavy smoker (>20 cigarettes per day or nicotine-equivalent) and/or is unable to abstain from smoking or unable to abstain from the use of prohibited nicotine-containing products for at least 1 hour before and 6 hours after study treatment administration (including e-cigarettes, pipes, cigars, chewing tobacco, nicotine topical patches, nicotine gum, or nicotine lozenges),

11. Is a heavy opioid user and not likely to be sensitive to a 20 mg dose of oxycodone, in the opinion of an investigator or designee,

12. Regularly consumes excessive amounts of caffeine or xanthines within 30 days prior to screening, defined as greater than 6 servings (1 serving is approximately equivalent to 120 mg of caffeine) of coffee, tea, cola, or other caffeinated beverages per day,

13. History of suicidal ideation or suicidal behaviour within 2 years of screening, showing suicidal tendency as per the Columbia Suicide Severity Rating Scale (C-SSRS) administered at screening, or is currently at risk of suicide in the opinion of an investigator,

14. Presence of clinically significant ECG abnormalities at the screening visit, as defined by medical judgment, Note: QT corrected according to Fridericia's formula (QTcF) interval of >450 msec in male subjects or >470 msec in female subjects will be exclusionary. The ECG may be repeated once for confirmatory purposes if the initial value obtained exceeds the limits specified,

15. Has creatinine clearance ≤60ml/min as calculated by the Cockcroft-Gault equation,

16. Any history of tuberculosis,

17. Positive screening results to human immunodeficiency virus (HIV) 1 and 2 antibodies, hepatitis B virus surface antigen (HBsAg) or hepatitis C virus antibody (HCVAb) tests,

18. Intake of an investigational product (IP) within 30 days or 5 times the half-life (whichever is longer) prior to screening,

19. Use of any prescription drugs (with the exception of hormonal contraceptives or hormone replacement therapy) in the 30 days prior to the first study treatment administration, that in the opinion of an investigator would put into question the status of the subject as healthy,

20. Use of over-the-counter (OTC) products (including herbal preparations and supplements) within 7 days prior to the first study treatment administration, with the exception of ibuprofen or acetaminophen,

21. Use of a prohibited medication as specified in section 4.7,

22. Donation of plasma in the 7 days prior to screening,

23. Blood donation (excluding plasma) of approximately 500 mL of blood in the 56 days prior to screening,

24. Is, in the opinion of an investigator or designee, considered unsuitable or unlikely to comply with the study protocol for any reason.

25. Poor venous access at screening, as judged by an investigator.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Arbor Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Altasciences Clinical Kansas

Overland Park, Kansas, United States

Countries

United States

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

AR26.3031.2

Identifier Type: -

Identifier Source: org_study_id