Abuse Potential of Oral Gabapentin in Healthy, Non-Drug-Dependent Individuals With Recreational Sedative Drug Use Experience
A Phase 4, Randomized, Double-Blind, Placebo and Active-Controlled, Single-Dose, Four-Way Crossover Study Evaluating the Abuse Potential of Two Doses of Gabapentin Taken Orally in Healthy, Non-Drug-Dependent Participants With Sedative Drug Use Experience
Aperçu de l'étude
Statut
Statut
Les conditions
Les conditions
Intervention / Traitement
Intervention / Traitement
Description détaillée
Type d'étude
Type d'étude
Inscription (Réel)
Inscription
Phase
Phase
- Phase 4
Contacts et emplacements
Coordonnées de l'étude
Coordonnées de l'étude
- Nom: Dik Ng
- Numéro de téléphone: (+44) 1304626895
- E-mail: Dik.Ng@viatris.com
Sauvegarde des contacts de l'étude
- Nom: Laura Zachwieja
- Numéro de téléphone: (+1) 304 5992595
- E-mail: Laura.Zachwieja@viatris.com
Lieux d'étude
-
-
Kansas
-
Overland Park, Kansas, États-Unis, 66212
- Dr. Vince Clinical Research
-
-
Critères de participation
Critère d'éligibilité
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
La description
Inclusion Criteria:
- Male and female participants must be 18 to 55 years of age, inclusive, at the time of screening. At least 20% of participants randomized into the Treatment Phase should be female.
Male participants must agree to the following requirements during the intervention period and for at least 93 days after the last dose of study intervention, which corresponds to the time needed to eliminate study intervention(s) plus an additional 90 days (a spermatogenesis cycle):
• Refrain from donating sperm.
PLUS either:
- Be abstinent from heterosexual intercourse as their preferred and usual lifestyle (abstinent on a long term and persistent basis) and agree to remain abstinent; OR
- Must agree to use contraception/barrier as detailed below:
- Agree to use a male condom and spermicide when engaging in any activity that allows for passage of ejaculate to another person.
Male participants should be advised of the benefit for a female partner to use a highly effective method of contraception, as a condom may break or leak when having sexual intercourse with a woman of child-bearing potential (WOCBP) who is not currently pregnant.
- A female participant is eligible to participate if she is not pregnant or breastfeeding, and at least 1 of the following conditions applies:
- Is not a WOCBP; OR
- Is a WOCBP and using a contraceptive method
- A WOCBP agrees not to donate eggs (ova, oocytes) for the purpose of reproduction during the study and for 30 days after the last dose of investigational product. The investigator should evaluate the effectiveness of the contraceptive method in relationship to the first dose of study intervention.
- Participants who are overtly healthy. Healthy is defined as no clinically relevant abnormalities identified by a detailed medical history, complete physical examination, vital signs, 12-lead electrocardiogram (ECG), and/or clinical laboratory tests.
- Participants must be recreational sedative drug users, defined as those reporting using a sedative agent (e.g., barbiturates, benzodiazepines) for its intoxicating effects on at least 10 lifetime occasions and at least once in the 12 weeks before the Screening Visit, but who have no signs of dependence and are not seeking treatment for their sedative use.
- Participants must satisfactorily complete the Drug Discrimination phase.
- Body mass index (BMI) of 17.5 to 34 kg/m2, inclusive; and a total body weight ≥50 kg (110 lb).
Exclusion Criteria:
- Participants with current or past diagnosis of any type of drug dependence within the past year. Diagnosis of substance and/or alcohol dependence (excluding caffeine and nicotine) will be assessed by the Investigator using the Diagnostic and Statistical Manual of Mental Disorders-5-Text Revision (DSM-5-TR) criteria performed at Screening. Current drug use will be allowed if the candidate can produce a negative urine sample (excluding THC) prior to first dose and are free of any signs/symptoms of withdrawal. The candidate will be informed if they have a positive breathalyzer or urine ethanol test.
- Participants who are heavy smokers (>20 cigarettes equivalents per day)
- Participants who are unable to abstain from smoking for at least 2 hours before and at least 8 hours after study drug administration.
- Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurological, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at the time of dosing).
- Participants with any history of sleep apnea, myasthenia, or glaucoma.
- Any condition possibly affecting drug absorption (e.g., gastrectomy) excluding cholecystectomy within 1 year prior to study.
- Participants with a positive test for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C antibody (HCVAb).
- Participants with active suicidal ideation or suicidal behavior within 5 years prior to Screening as determined through the use of the Columbia Suicide Severity Rating Scale (C-SSRS) or active ideation identified at Screening or on Day -1.
- Other acute or chronic medical or psychiatric condition including recent (within the past year) or active suicidal ideation or behavior or clinically significant laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the participant inappropriate for entry into this study.
- Use of prescription or nonprescription drugs and dietary supplements within 7 days or 5 half-lives (whichever is longer) prior to the first dose of investigational product. (Refer to Section 6.8 for additional details).
- Herbal supplements and herbal medications must be discontinued at least 14 days prior to the first dose of study medication.
- Previous administration with an investigational drug within 30 days (or as determined by the local requirement) or 5 half-lives (whichever is longer) prior to screening.
- Positive urine drug screen (UDS) for substances of abuse at admission to the Qualification Phase, excluding tetrahydrocannabinol (THC). If a participant presents with a positive UDS (excluding THC) at admission or any visit, the investigator, at his/her discretion, may reschedule a repeat UDS until the UDS is negative (excluding THC) before the participant is permitted to be dosed in any phase of the study.
- Participants who are unable to abstain from using THC during the inpatient stays in the Qualification and Treatment Phases of the study.
- Has participated in, is currently participating in, or is seeking treatment for substance and/or alcohol related disorders (excluding nicotine and caffeine). If participation in a rehabilitation program was court-mandated as part of a plea agreement, entry may be permissible at the Investigator's discretion.
- Has a positive urine ethanol test upon admission to the study center. Positive results may be repeated and/or participants rescheduled at the Investigator's discretion.
- Screening sitting BP 145 mm Hg (systolic) or 95 mm Hg (diastolic), following at least 5 minutes of rest. If BP is 145 mm Hg (systolic) or 95 mm Hg (diastolic), the BP should be repeated 2 more times and the average of the 3 BP values should be used to determine the participant's eligibility. Repeated BP tests should be spaced at least 5 minutes apart.
- Baseline (screening) 12 lead ECG that demonstrates clinically relevant abnormalities that may affect participant safety or interpretation of study results (e.g., baseline corrected QT (QTc) interval as determined by the Fridericia method (QTcF) >450 msec (males) or >470 msec (females), complete left bundle branch block [LBBB], signs of an acute or indeterminate-age myocardial infarction, ST T interval changes suggestive of myocardial ischemia, second- or third-degree atrioventricular [AV] block, or serious bradyarrhythmias or tachyarrhythmias). If QTcF exceeds 450 msec (males) or 470 msec (females), or QRS exceeds 120 msec, the ECG should be repeated 2 more times and the average of the 3 QTcF or QRS values should be used to determine the participant's eligibility. Computer-interpreted ECGs should be overread by an Investigator experienced in reading ECGs before excluding participants.
Participants with ANY of the following abnormalities in clinical laboratory tests at screening, as assessed by the study-specific laboratory and confirmed by a single repeat test, if deemed to be clinically significant in the opinion of the investigator:
- Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) level 1.5 × upper limit of normal (ULN);
- Total bilirubin level 1.5 × ULN; participants with a history of Gilbert's syndrome may have direct bilirubin measured and would be eligible for this study provided the direct bilirubin level is ULN.
- Blood donation (excluding plasma donations) of approximately 1 pint (500 mL) or more within 56 days prior to dosing.
- History of sensitivity to heparin or heparin-induced thrombocytopenia.
- Unwilling or unable to comply with the criteria in the Lifestyle considerations section of the protocol.
- History of hypersensitivity to gabapentin or alprazolam or any of the components in the formulation of the study products.
- Investigator site staff members directly involved in the conduct of the study and their family members, site staff members otherwise supervised by the investigator, or Sponsor employees, including their family members, directly involved in the conduct of the study.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Autre
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Double
Nombre de bras
Armes et Interventions
Groupe de participants / BrasGroupe de participants / Bras |
Intervention / TraitementIntervention / Traitement |
|---|---|
|
Comparateur actif: Treatment Phase A
|
2mg
|
|
Comparateur placebo: Treatment Phase B
|
placebo
|
|
Comparateur actif: Treatment Phase C
|
1200mg
1800mg
|
|
Comparateur actif: Treatment Phase D
|
1200mg
1800mg
|
Que mesure l'étude ?
Principaux critères de jugement
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Bipolar Visual Analog Scale (VAS) for "Drug Liking" Maximum Effect (Emax)
Délai: Up to 24 hours after treatments
|
Drug liking assesses how much a participant likes or dislikes a drug effect at the time the question is being asked.
It is scored using a 100 mm visual analogue scale (VAS), where 0 mm = "Strong Disliking", 50 mm = "Neither Like nor Dislike", and 100 mm = "Strong Liking"
|
Up to 24 hours after treatments
|
Mesures de résultats secondaires
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Bipolar VAS for "Drug Liking" (Time for Emax [TEmax])
Délai: Up to 24 hours after treatments
|
Time after dosing when the maximum effect for Drug Liking VAS is reached
|
Up to 24 hours after treatments
|
|
Bipolar VAS for "Drug Liking" (Area Under the Effect-time Profile From Time 0 to the Time of the Last Quantifiable Effect [AUEClast])
Délai: Up to 24 hours after treatments (Assessments were made at the following timepoints after each treatment: 0, 0.25, 0.5,1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12 and 24 hours)
|
Area under the effect-time profile from time 0 to the time of the last available data for the "Drug liking" visual analog scale which assesses how much a participant likes or dislikes a drug effect at the time the question ("at this moment, my liking this drug is") is being asked.
It is scored using a 100 mm visual analogue scale (VAS), where 0 mm = "Strong Disliking", 50 mm = "Neither Like nor Dislike", and 100 mm = "Strong Liking".
The minimum and maximum possible scores are approximately 0 and 2400 if a subject scores 0 mm (strong disliking) and 100 mm (strong liking) respectively at every timepoint up to 24 hours.
|
Up to 24 hours after treatments (Assessments were made at the following timepoints after each treatment: 0, 0.25, 0.5,1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12 and 24 hours)
|
|
Unipolar VAS for "High" (Maximum Effect, Emax)
Délai: Up to 24 hours after treatments
|
Maximum effect on the 100 mm visual analog scale for the question "I am feeling high" where 0 = "not at all" and 100 = "extremely"
|
Up to 24 hours after treatments
|
|
Unipolar VAS for "High" (Time for Emax [TEmax])
Délai: Up to 24 hours after treatments
|
Time after dosing when the maximum effect for "High" VAS is reached
|
Up to 24 hours after treatments
|
|
Unipolar VAS for "High" (Area Under the Effect-time Profile From Time 0 to the Time of the Last Quantifiable Effect [AUEClast])
Délai: Up to 24 hours after treatments (Assessments were made at the following timepoints after each treatment: 0, 0.25, 0.5,1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12 and 24 hours)
|
Area under the effect-time profile from time 0 to the time of the last available data for the "High" visual analog scale which measures on a 100 mm visual analog scale the subject's response to the question "I am feeling high" where 0 = "not at all" and 100 = "extremely".
The minimum and maximum possible scores are 0 and approximately 2400 if a subject scores 0 mm (not at all) and 100 mm (extremely) respectively at every timepoint up to 24 hours.
|
Up to 24 hours after treatments (Assessments were made at the following timepoints after each treatment: 0, 0.25, 0.5,1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12 and 24 hours)
|
|
Bipolar VAS for "Take Drug Again"
Délai: at 12 and 24 hours after treatments
|
100 mm visual analog scale for the question "I would take this drug again" where 0 = "definitely not", 50 = "neutral", and 100 = "definitely so".
|
at 12 and 24 hours after treatments
|
|
Bipolar VAS for "Overall Drug Liking"
Délai: at 12 and 24 hours after treatments
|
100 mm visual analog scale for the question "Overall, my liking for this drug is" where0 = "definitely not", 50 = "neutral", and 100 = "definitely so".
|
at 12 and 24 hours after treatments
|
|
Pharmacokinetics of gabapentin
Délai: Up to 24 hours after treatments (concentrations were measured at the following timepoints after each treatment for this outcome measure: 0, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12 and 24hours)
|
Maximum plasma concentration (Cmax), time when the maximum concentration is reached (Tmax), and Area Under the concentration time profile from time 0 to the time of the last quantifiable concentration (AUClast) for gabapentin measured from blood samples
|
Up to 24 hours after treatments (concentrations were measured at the following timepoints after each treatment for this outcome measure: 0, 0.25, 0.5, 1, 1.5, 2, 2.5, 3, 3.5, 4, 6, 8, 12 and 24hours)
|
Collaborateurs et enquêteurs
Parrainer
Parrainer
Collaborateurs
Collaborateurs
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Début de l'étude
Achèvement primaire (Réel)
Achèvement primaire
Achèvement de l'étude (Réel)
Achèvement de l'étude
Dates d'inscription aux études
Première soumission
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Première publication
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour publiée
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Acides aminés, peptides et protéines
- Produits chimiques organiques
- Composés hétérocycliques
- Composés hétérocycliques, 2 anneaux
- Composés hétérocycliques, anneau fusionné
- Hydrocarbures
- Cyclohexanes
- Cycloparaffines
- Hydrocarbures, alicyclique
- Hydrocarbures, cyclique
- Acides, acyclique
- Acides carboxyliques
- Amines
- Acides aminés
- Benzazépines
- acide gamma-aminobutyrique
- Aminobutyrate
- Butyrate
- Acides, carbocyclique
- Benzodiazépines
- Acides cyclohexanecarboxyliques
- Gabapentine
- Alprazolam
Autres numéros d'identification d'étude
Autres numéros d'identification d'étude
- GABA-TBZ-4002
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .