- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02245438
Effect of Tipranavir and Ritonavir on the Pharmacokinetic Characteristics of Norethindrone-Ethinyl Estradiol in Healthy Female Adult Volunteers
18. september 2014 oppdatert av: Boehringer Ingelheim
A Single Centre, Open-label, Randomized, Parallel Group, Multiple Dose Comparison of the Effect of TPV 750 mg and RTV 200 mg or TPV 500 mg and RTV 100 mg, Administered Twice Daily, on the Pharmacokinetic Characteristics of Norethindrone-Ethinyl Estradiol (Ortho®-1/35 ) Administered as a Single Dose, in Healthy Female Adult Volunteers.
Study to characterize the effects of two dose combinations of Tipranavir (TPV)/Ritonavir (RTV) (TPV 750 mg/RTV 200 mg and TPV 500 mg/RTV 100 mg), administered twice-daily, on the pharmacokinetics of Norethindrone-Ethinyl Estradiol (NET/EE) 1 mg/ 0.035 mg administered as a single dose.
Studieoversikt
Status
Avsluttet
Forhold
Studietype
Intervensjonell
Registrering (Faktiske)
52
Fase
- Fase 1
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 50 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Hunn
Beskrivelse
Inclusion Criteria:
- Female subjects between 18 and 50 years of age inclusive
- A Body Mass Index (BMI) between 18 and 29 kg/m2
- Signed informed consent prior to trial participation
- Ability to swallow numerous large capsules without difficulty
- Acceptable laboratory values that indicate adequate baseline organ function are required at the time of screening. Laboratory values are considered to be acceptable if severity is less than or equal to Grade 1, based on the AIDS Clinical Trials Group Grading Scale. All abnormal laboratory values greater than Grade 1 are subject to approval by the trial clinical monitor.
- Acceptable medical history, physical examination and ECG, and chest X-ray (if not conducted within the last 12 months) are required prior to entering the treatment phase of the study
- Willingness to abstain from alcohol for 48 hours prior to Study Day 0 and abstain from alcohol for the duration of the study. In addition, red wine must not have been ingested within 5 days prior to Day 0 (Visit 2)
- Willingness to abstain from ingesting grapefruit, grapefruit juice, or products containing grapefruit juice, within 10 days before Day 0, Visit 2 and for the duration of the study
- Willingness to abstain from ingesting Seville oranges, garlic supplements, St. John's Wort, Milk Thistle, or methylxanthine-containing drinks or food (coffee, tea, cola, energy drinks, chocolate, etc) within 5 days of Day 0, Visit 2 and for the duration of the study
- Willingness to abstain from over the counter herbal medications for the duration of the study
- Reasonable probability for completion of the study
Exclusion Criteria:
Female subjects who are of reproductive potential who:
- Have positive serum beta-human chorionic gonadotropin at Visit 1, or on Day 0 or Day 1
- Have not been using a barrier contraceptive method for at least 3 months prior to Visit 3 (Day 1)
- Are not willing to use a reliable method of double-barrier contraception (such as diaphragm with spermicidal cream/jelly or condoms with spermicidal foam), during the trial and 30 days after completion/termination
- Are breast-feeding
- Participation in another trial with an investigational medicine within 30 days prior to Day 0 (Visit 2)
- Use of any medication listed in the protocol within 30 days prior to Day 0 (Visit 2)
- Use of any other pharmacological contraceptive (including oral, patch or injectable contraceptives) for 1 month prior to study initiation and for the duration of the study
- Administration of antibiotics within 10 days prior to Day 0 (Visit 2) or during the trial
- History of central nervous system (CNS), gastrointestinal, hepatic, or renal disorders within the past sixty (60) days. Subjects will be excluded for these disorders greater than sixty days if, in the opinion of the investigator, the subject does not qualify as a healthy volunteer
- History of thrombotic disease
- History of migraine headache
- Have serological evidence of hepatitis B or C virus
- Have serological evidence of exposure to HIV
- Recent history of alcohol or substance abuse (within 6 months of study period)
- Cigarette smoking (greater than 10 cigarettes per day)
- Blood or plasma donations within 30 days prior to Day 0 (Visit 2) or during the trial.
- Subjects with a seated systolic blood pressure either <100 mm Hg or >150 mm Hg; resting heart rate either <50 beats/min or >90 beats/min. For subjects with a resting heart rate below 50, due to a high fitness level, the investigator may discuss exclusion with the medical monitor on a case-by-case basis
- Subjects with a history of any illness or allergy that, in the opinion of the investigator, might confound the results of the study or pose additional risk in administering Tipranavir, Ritonavir or NET/EE to the subject
- Subjects who have had an acute illness within 2 weeks prior to Day 0 (Visit 2)
- Subjects who are currently taking any over-the-counter drug within 7 days prior to Day 0,(Visit 2) or who are currently taking any prescription drug that, in the opinion of the investigator in consultation with the clinical monitor, might interfere with either the absorption, distribution or metabolism of the test substances
- Known hypersensitivity to TPV, RTV, or NET/EE
- Inability to comply with the protocol
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: TPV/RTV low dose
|
Andre navn:
Andre navn:
|
|
Eksperimentell: TPV/RTV high dose
|
Andre navn:
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Area under plasma concentration time curve
Tidsramme: up to day 17
|
up to day 17
|
|
Maximum plasma concentration of the analyte
Tidsramme: up to day 17
|
up to day 17
|
|
Drug concentration of the analyte in plasma at 12 hours after administration
Tidsramme: up to day 17
|
up to day 17
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Oral clearance of the analyte
Tidsramme: up to day 17
|
up to day 17
|
|
Time of maximum concentration of the analyte
Tidsramme: up to day 17
|
up to day 17
|
|
Apparent terminal half life of the analyte
Tidsramme: up to day 17
|
up to day 17
|
|
Number of subjects with adverse events
Tidsramme: up to 45 days
|
up to 45 days
|
|
Number of subject with clinically relevant changes in laboratory parameters
Tidsramme: up to 17 days
|
up to 17 days
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
Hjelpsomme linker
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
1. mai 2002
Primær fullføring (Faktiske)
1. juni 2002
Datoer for studieregistrering
Først innsendt
18. september 2014
Først innsendt som oppfylte QC-kriteriene
18. september 2014
Først lagt ut (Anslag)
19. september 2014
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
19. september 2014
Siste oppdatering sendt inn som oppfylte QC-kriteriene
18. september 2014
Sist bekreftet
1. september 2014
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
- Fysiologiske effekter av legemidler
- Molekylære mekanismer for farmakologisk virkning
- Anti-infeksjonsmidler
- Antivirale midler
- Enzymhemmere
- Anti-HIV-midler
- Antiretrovirale midler
- Hormoner
- Hormoner, hormonsubstitutter og hormonantagonister
- Proteasehemmere
- Østrogener
- Cytokrom P-450 CYP3A-hemmere
- Cytokrom P-450 enzymhemmere
- Prevensjonsmidler, hormonelle
- Prevensjonsmidler
- Reproduktive kontrollmidler
- Prevensjonsmidler, orale, kombinert
- Prevensjonsmidler, Oral
- Prevensjonsmidler, kvinner
- Prevensjonsmidler, orale, syntetiske
- HIV-proteasehemmere
- Virale proteasehemmere
- Prevensjonsmidler, orale, hormonelle
- Ritonavir
- Østradiol
- Etinylestradiol
- Tipranavir
- Norethindron
- Norethindroneacetat
- Norinyl
Andre studie-ID-numre
- 1182.22
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. .