- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01706796
A Study Comparing PF-06273340 Immediate Release Tablet, PF-06273340 Modified Release Tablets To PF-06273340 Oral Solution In The Fasted State. This Study Will Also Compare PF-06273340 Modified Release Tablets In Fasted And Fed State
23. januar 2013 opdateret af: Pfizer
A Phase 1, Open Label, Randomized, Single Dose, 5 Period Crossover Relative Bioavailability Study In Healthy Volunteers Evaluating Spray Dried Dispersion (SDD) Immediate Release (IR) PF-06273340 Tablet, Two SDD Modified Release (MR) Matrix Tablets In Comparison With PF-06273340 Oral Solution, Including Preliminary Assessment Of Food Effect
The primary purpose of this study is to estimate the relative bioavailability and food effect of PF-06273340 tablets.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
12
Fase
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Singapore, Singapore, 188770
- Pfizer Investigational Site
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Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
21 år til 55 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Healthy male and/or female subjects of non-child bearing potential, between the ages of 21 and 55 years, inclusive (Healthy is defined as no clinically relevant abnormalities identified by a detailed medical history, full physical examination, including blood pressure and pulse rate measurement, 12-lead ECG and clinical laboratory tests).
- Body Mass Index (BMI) of 17.5 to 30.5 kg/m2; and a total body weight >50 kg (110 lbs).
- An informed consent document signed and dated by the subject.
- Subjects who are willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures
Exclusion Criteria:
- Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing).
- Any condition possibly affecting drug absorption (eg, gastrectomy).
- A positive urine drug screen.
- History of regular alcohol consumption exceeding 14 drinks/week for females or 21 drinks/week for males (1 drink = 5 ounces (150 mL) of wine or 12 ounces (360 mL) of beer or 1.5 ounces (45 mL) of hard liquor) within 6 months of Screening.
- Use of tobacco- or nicotine-containing products in excess of the equivalent of 5 cigarettes per day.
- Treatment with an investigational drug within 30 days (or as determined by the local requirement, whichever is longer) or 5 half-lives preceding the first dose of study medication.
- Screening supine blood pressure >=140 mm Hg (systolic) or >=90 mm Hg (diastolic), on a single measurement (confirmed by a single repeat, if necessary) following at least 5 minutes of rest.
- Evidence or history of orthostatic hypotension.
- 12-lead ECG demonstrating QTc >450 or a QRS interval >120 msec at Screening. If QTc exceeds 450 msec, or QRS exceeds 120 msec, the ECG should be repeated two more times and the average of the three QTc values should be used to determine the subject's eligibility.
- Pregnant or nursing females; females of childbearing potential, including those with tubal ligation.
- Use of prescription or nonprescription drugs, vitamins and dietary supplements within 7 days or 5 half-lives (whichever is longer) prior to the first dose of study medication. Herbal supplements must be discontinued 28 days prior to the first dose of study medication. As an exception, acetaminophen/paracetamol may be used at doses of <=1 g/day. Limited use of non-prescription medications that are not believed to affect subject safety or the overall results of the study may be permitted on a case-by-case basis following approval by the sponsor.
- 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 Lifestyle guidelines described in this protocol.
- Other severe acute or chronic medical or psychiatric condition or 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 subject inappropriate for entry into this study.
- Subjects who are investigational site staff members or relatives of those site staff members or subjects who are Pfizer employees directly involved in the conduct of the trial.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Crossover opgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
---|---|
Eksperimentel: PF-06273340 Oral Solution Fasted
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Oral solution, single dose, fasted
Immediate Release Tablet, single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fasted
Modified Release Tablet (long duration, MR2), single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fed
Modified Release Tablet (long duration, MR2), single dose, fed
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Eksperimentel: PF-06273340 Immediate Release Tablet Fasted
|
Oral solution, single dose, fasted
Immediate Release Tablet, single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fasted
Modified Release Tablet (long duration, MR2), single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fed
Modified Release Tablet (long duration, MR2), single dose, fed
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Eksperimentel: PF-06273340 Modified Release (MR1) Tablet Fasted
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Oral solution, single dose, fasted
Immediate Release Tablet, single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fasted
Modified Release Tablet (long duration, MR2), single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fed
Modified Release Tablet (long duration, MR2), single dose, fed
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Eksperimentel: PF-06273340 Modified Release (MR2) Tablet Fasted
|
Oral solution, single dose, fasted
Immediate Release Tablet, single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fasted
Modified Release Tablet (long duration, MR2), single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fed
Modified Release Tablet (long duration, MR2), single dose, fed
|
Eksperimentel: PF-06273340 Modified Release (MR1) Tablet Fed
|
Oral solution, single dose, fasted
Immediate Release Tablet, single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fasted
Modified Release Tablet (long duration, MR2), single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fed
Modified Release Tablet (long duration, MR2), single dose, fed
|
Eksperimentel: PF-06273340 Modified Release (MR2) Tablet Fed
|
Oral solution, single dose, fasted
Immediate Release Tablet, single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fasted
Modified Release Tablet (long duration, MR2), single dose, fasted
Modified Release Tablet (short duration, MR1), single dose, fed
Modified Release Tablet (long duration, MR2), single dose, fed
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
---|---|
Maximum Observed Plasma Concentration (Cmax)
Tidsramme: up to 48 h post dose
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up to 48 h post dose
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Area Under the Curve From Time Zero to Last Quantifiable Concentration (AUClast)
Tidsramme: up to 48 h post dose
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up to 48 h post dose
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Area Under the Curve From Time Zero to Extrapolated Infinite Time [AUC (0 - 8)]
Tidsramme: up to 48 h post dose
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up to 48 h post dose
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Elimination half life
Tidsramme: up to 48 h post dose
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up to 48 h post dose
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Time to Reach Maximum Observed Plasma Concentration (Tmax)
Tidsramme: up to 48 h post dose
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up to 48 h post dose
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. november 2012
Primær færdiggørelse (Faktiske)
1. januar 2013
Studieafslutning (Faktiske)
1. januar 2013
Datoer for studieregistrering
Først indsendt
11. oktober 2012
Først indsendt, der opfyldte QC-kriterier
11. oktober 2012
Først opslået (Skøn)
15. oktober 2012
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
24. januar 2013
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
23. januar 2013
Sidst verificeret
1. januar 2013
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- B5261003
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med PF-06273340
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PfizerAfsluttet
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PfizerAfsluttet
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