- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02688374
A Bioequivalence Study of Three, 2 mg Nicotine Chewing Gums (Two Tests and One Reference) in Healthy Adult Smokers
18. desember 2017 oppdatert av: GlaxoSmithKline
A Single-Dose, Open-Label, Three-way Crossover Bioequivalence Study of Three, 2 mg Nicotine Chewing Gums (Two Tests and One Reference) in Chinese Male Healthy Adult Smokers
This is a randomized, open-label, single-dose, three-period, crossover, single-center comparative bioavailability (BA) study under fasting condition in Chinese healthy male adult participants with a history of cigarette smoking.
The participants will be admitted to the investigational clinic at least 38 hours before dosing and will remain domiciled until the completion of all study procedures at approximately 24 hours after dosing.
Three toothpastes (one is commercial non-medicated non-nicotine containing chewing gum and other two are nicotine containing gums) will be provided across the 3 treatment periods.
During each of the 3 treatment periods, participants will be under supervision in a non-smoking area and will abstain from smoking.There will be a total of at least 7 days and not more than 10 days (clinical furlough period) between treatment periods.
Twenty (20) blood samples will be collected for pharmacokinetic (PK) analysis at baseline and multiple time points following study drug administration.
The trial duration will be approximately 49 days and up to 55 days from screening to study end including the screening period.
Studieoversikt
Status
Fullført
Forhold
Studietype
Intervensjonell
Registrering (Faktiske)
45
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
-
Beijing, Kina, 100032
- GSK Investigational Site
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 45 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Mann
Beskrivelse
Inclusion Criteria:
- Participants must understand and provide written informed consent before any assessment is performed, understand the study procedures, and be willing to complete the required assessments and the study.
- Chinese male participants between 18 and 45 years of age (inclusive) in general good physical health as judged by the Investigator.
- Normal vital signs as follows:
- Oral body temperature between 35.0 and 37.5 ºC (95 and 99.5 F) inclusive
- Supine systolic blood pressure between 90 and 140 mmHg inclusive
- Supine diastolic blood pressure between 55 and 90 mmHg inclusive
- Pulse rate between 50 and 100 beats per minute (bpm) inclusive
- History of cigarette smoking of at least 10 cigarettes per day continuously for the past 3 months prior to screening.
- Body weight ≥ 50 kg, Body Mass Index (BMI) between 19 and 28 at screening.
- Ability to communicate and comply with all study requirements including the study specific chewing and swallowing procedures.
Exclusion Criteria:-
- Use of other investigational drugs within 30 days or 10 half-lives of enrollment, whichever is longer.
- History of or known hypersensitivity to the study drug or excipients.
- Diagnosis of long QT syndrome or QTc > 450 msec for males at screening.
- Any surgical or medical condition which may significantly alter the absorption, distribution, metabolism or excretion of any drug substance.
- History of malignancy or neoplastic disease of any organ system treated or untreated, orthostatic hypotension, cardiovascular disease, stroke, TIA, fainting or blackouts, clinically significant metabolic, pulmonary, neurological, hematological, autoimmune, psychiatric or endocrine disorders.. within the past 5 years prior to screening.
- Any evidence of cardiovascular, pulmonary, renal, hepatic, gastrointestinal, hematological, endocrinological, metabolic, autoimmune, neurological, psychiatric, other diseases or other clinically significant laboratory findings at screening.
- Participant has used any medication within two weeks before first scheduled study drug administration or within less than 10 times the elimination half-life of the respective drug.
- Unable to comply with the chewing and/or swallowing rhythm requirements (> 5% deviation of the total counts over 30 minutes) after trying either one of the two training sessions for 3 times.
- CO > 12 ppm after at least 38 hours confinement period in clinics prior to first dosing.
- Participants reports consumption of any drug metabolizing enzyme inducing or inhibiting aliments, evidence of current alcohol abuse or reports consumption exceeding 35 g of pure alcohol per day.
- Any history of drug hypersensitivity, asthma, urticaria, or other significant allergic diathesis, positive results in any of the virology tests for Human immunodeficiency virus (HIV)-Ab, Hepatitis C virus (HCV)-Ab, Surface antigen of the hepatitis B virus (HBs-Ag), and Tp-Ab.
- Participation in a previous clinical study with or without another investigational product and with ~470 ml blood drawn, or blood donation within the last 3 months prior to screening or previous enrollment into the current study.
- Vulnerable individual
- Inability to be venipuncture and/or tolerate venous access, unwilling to accept slight irritation of the throat and increased salivation due to nicotine gum administration.
- Unable or unwilling to discontinue the use or consumption of cigarette smoking, any nicotine containing products, Oral, local or topical pharmaceutical agents, consumption of caffeine/theophylline - containing products, grapefruit, Seville orange, orange, lemon, lime, apple, and pineapple, performance of unaccustomed strenuous physical exercise.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Annen
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Annen: Treatment A:Treatment B:Treatment C
Participants will be administered with Treatment A(Nicorette 2 mg coated mint gum) followed by Treatment B (Nicotinell 2 mg coated mint gum) followed by Treatment C (Nicotinell 2 mg coated fruit flavor gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
Annen: Treatment B:Treatment C:Treatment A
Participants will be administered with Treatment B (Nicotinell 2 mg coated mint gum) followed by Treatment C (Nicotinell 2 mg coated fruit flavor gum) followed by Treatment A(Nicorette 2 mg coated mint gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
Annen: Treatment C:Treatment A:Treatment B
Participants will be administered with Treatment C (Nicotinell 2 mg coated fruit flavor gum) followed by Treatment A(Nicorette 2 mg coated mint gum) followed by Treatment B (Nicotinell 2 mg coated mint gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
Annen: Treatment A: Treatment C:Treatment B
Participants will be administered with Treatment A (Nicorette 2 mg coated mint gum) followed by Treatment C (Nicotinell 2 mg coated fruit flavor gum) followed by Treatment B (Nicotinell 2 mg coated mint gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
Annen: Treatment B:Treatment A: Treatment C
Participants will be administered with Treatment B (Nicotinell 2 mg coated mint gum) followed by Treatment A (Nicorette 2 mg coated mint gum) followed by Treatment C (Nicotinell 2 mg coated fruit flavor gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
Annen: Treatment C:Treatment B:Treatment A
Participants will be administered with Treatment C (Nicotinell 2 mg coated fruit flavor gum) followed by Treatment B (Nicotinell 2 mg coated mint gum) followed by Treatment A (Nicorette 2 mg coated mint gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Area under the curve from time zero to last sampling time [AUC(0-t)]
Tidsramme: 2 days
|
AUC(0-t) will be calculated using the trapezoidal rule.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Area under the curve from time zero extrapolated to infinity [AUC(0-inf)]
Tidsramme: 2 days
|
The area under the plasma concentration versus time curve will be calculated from time 0 to infinity where AUC = AUClast + Clast/λz Clast is the concentration at the last measurable sampling time point and λz is the terminal elimination rate constant.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Maximum plasma concentration (Cmax)
Tidsramme: 2 days
|
Cmax will be obtained graphically from the plasma concentration over time profile.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Time to reach maximum plasma concentration (Tmax)
Tidsramme: 2 days
|
Tmax will be obtained graphically from the plasma concentration over time profile.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Termination rate constant (Lambda_z)
Tidsramme: 2 days
|
Lambda_z will be computed as the slope of the regression line of ln (C(t)) on time.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Elimination half life (t1/2)
Tidsramme: 2 days
|
T1/2 will be computed as T1/2 = 0.693/ λz.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Systemic clearance (CL/F)
Tidsramme: 2 days
|
CL/F will be calculated as the Dose/AUCinf, where Dose is the actual nicotine dose released.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Apparent volume of distribution (Vd/F)
Tidsramme: 2 days
|
Vd/F will be determined by the following equation: Vz/F = Dose/(lambda_z · AUCinf), where Dose is the actual nicotine dose released.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
11. mars 2016
Primær fullføring (Faktiske)
12. juni 2016
Studiet fullført (Faktiske)
12. juni 2016
Datoer for studieregistrering
Først innsendt
18. februar 2016
Først innsendt som oppfylte QC-kriteriene
18. februar 2016
Først lagt ut (Anslag)
23. februar 2016
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
19. desember 2017
Siste oppdatering sendt inn som oppfylte QC-kriteriene
18. desember 2017
Sist bekreftet
1. desember 2017
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Psykiske lidelser
- Kjemisk-induserte lidelser
- Stoffrelaterte lidelser
- Tobakksbruksforstyrrelse
- Fysiologiske effekter av legemidler
- Nevrotransmittere agenter
- Molekylære mekanismer for farmakologisk virkning
- Autonome agenter
- Agenter fra det perifere nervesystemet
- Kolinerge midler
- Ganglioniske stimulerende midler
- Nikotiniske agonister
- Kolinerge agonister
- Nikotin
Andre studie-ID-numre
- 204979
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .