- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02118909
Evaluate the Effects of Itraconazole and Ciprofloxacin on Single-Dose PK of Pracinostat in Healthy Nonsmoking Subjects
22. februar 2017 opdateret af: Helsinn Healthcare SA
A Two-Part Study to Evaluate the Effect of CYP3A4 Inhibition (Itraconazole-Part 1) and CYP1A2 Inhibition (Ciprofloxacin - Part 2) on the Single-Dose Pharmacokinetics of Pracinostat in Healthy Nonsmoking Subjects
This study is designed as a 2-part, open-label study to assess the effect of pracinostat with itraconazole (part 1) and pracinostat with ciprofloxacin (part 2) on the bioavailability of pracinostat.
Secondarily to evaluate the safety and tolerability of pracinostat administered with itraconazole or ciprofloxacin.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
32
Fase
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Arizona
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Tempe, Arizona, Forenede Stater, 67296
- Celerion
-
-
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
18 år til 55 år (Voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Healthy volunteer
- Continuous nonsmoker who has not used nicotine-containing products for at least 3 months prior to the first dose
- Body Mass Index (BMI) ≥ 18.5 and ≤ 32.0 kg/m2 at screening.
- Medically healthy with no clinically significant medical history, physical examination, laboratory profiles, vital signs or ECGs, as deemed by the PI.
- Female subjects must be of non-childbearing potential and must have undergone sterilization procedures at least 6 months prior to the first dose or be postmenopausal with amenorrhea for at least 1 year prior to the first dose and follicle stimulating hormone (FSH) serum levels consistent with postmenopausal status.
- A non vasectomized, male subject must agree to use a condom with spermicide or abstain from sexual intercourse during the study until 90 days beyond the last dose of study medication.
- Understands the study procedures in the informed consent form (ICF), and be willing and able to comply with the protocol.
Exclusion Criteria:
- Subject is mentally or legally incapacitated or has significant emotional problems at the time of screening visit or expected during the conduct of the study.
- History or presence of clinically significant medical or psychiatric condition or disease in the opinion of the PI.
- History of any illness that, in the opinion of the PI, might confound the results of the study or poses an additional risk to the subject by their participation in the study.
- History or presence of alcoholism or drug abuse within the past 2 years prior to screening.
- History or presence of hypersensitivity or idiosyncratic reaction to the study medication or related compounds.
- History of prolonged QT syndrome or require any current medications which may prolong QTc.
History or presence of:
- myasthenia gravis;
- convulsions.
- Female subjects who are pregnant or lactating.
- Positive urine cotinine, drug and alcohol results at screening or check-in.
- Positive results at screening for HIV, HBsAg or HCV.
- Seated blood pressure is less than 90/40 mgHg or greater than 140/90 mmHg at screening.
- Seated heart rate is lower than 40 bpm or higher than 99 bpm at screening.
- QTcF interval, is >430 msec (males) or >450 msec (females) or deemed clinical abnormal by the PI at screening or prior to dosing.
Unable to refrain from or anticipates the use of:
- Any drug, including prescription and non-prescription medications, tobacco, antacids, herbal remedies, or vitamin supplements beginning approximately 14 days prior to the first dose of study medication and throughout the study. Hormone replacement therapy will be allowed if postmenopausal females are on a stable treatment for at least 1 month prior to dosing on Day 1 of Period 1. Acetaminophen (up to 2 g per 24 hour period) may be permitted during the study.
- Any drugs known to be significant inducers of CYP enzymes, including St. John's Wort, for 28 days prior to the first dose of study medication and throughout the study. Appropriate sources will be consulted by the PI or designee to confirm lack of PK/pharmacodynamics interaction with study medication.
- Have been on a diet incompatible with the on-study diet, in the opinion of the PI, within the 28 days prior to the first dose of study medication(s), and throughout the study.
- Hemoglobin, platelet count or absolute neutrophils below the lower limit of normal at screening.
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) above upper limit of normal at screening.
- Donation of blood or significant blood loss within 56 days prior to the first dose of study medication.
- Participation in another clinical trial within 28 days prior to the first dose of study medication.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Part 1 (Pracinostat + Itraconazole)
Single-dose pracinostat and itraconazole dosing every day for 8 days
|
|
|
Eksperimentel: Part 2 (Pracinostat + Ciprofloxacin)
Single dose pracinostat and ciprofloxacin 2 times a day for 7 days
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Peak plasma concentration Cmax in healthy nonsmoking subjects given a single-dose of pracinostat
Tidsramme: pre-dose, 0.25, 0.5, 1, 1.25, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, 24, 36, 48, 72, 96 hours
|
Plasma PK parameter Cmax to describe bioavailability of pracinostat
|
pre-dose, 0.25, 0.5, 1, 1.25, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, 24, 36, 48, 72, 96 hours
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of participants with Adverse Events as a measure of safety and tolerability of single-dose pracinostat when administered with itraconazole or with ciprofloxacin in healthy nonsmoking adult subjects.
Tidsramme: 1 month
|
Safety will be monitored through physical examinations, vital sign measurements, electrocardiograms, adverse events, and clinical laboratory tests.
|
1 month
|
|
Peak plasma PK concentration Area Under the Curve (AUC)AUC 0-t, AUC 0-inf in healthy nonsmoking subjects given a single dose of pracinostat
Tidsramme: pre-dose, 0.25, 0.5, 1, 1.25, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, 24, 36, 48, 72, 96 hours
|
Plasma PK parameter AUC 0-t, AUC 0-inf for pracinostat
|
pre-dose, 0.25, 0.5, 1, 1.25, 1.5, 2, 2.5, 3, 4, 6, 8, 12, 16, 24, 36, 48, 72, 96 hours
|
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.
Hjælpsomme links
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. maj 2014
Primær færdiggørelse (Faktiske)
1. juni 2014
Studieafslutning (Faktiske)
1. august 2014
Datoer for studieregistrering
Først indsendt
11. april 2014
Først indsendt, der opfyldte QC-kriterier
17. april 2014
Først opslået (Skøn)
21. april 2014
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
23. februar 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
22. februar 2017
Sidst verificeret
1. februar 2017
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Anti-infektionsmidler
- Enzymhæmmere
- Antineoplastiske midler
- Hormoner, hormonsubstitutter og hormonantagonister
- Topoisomerase II-hæmmere
- Topoisomerasehæmmere
- Antibakterielle midler
- Cytokrom P-450 CYP3A-hæmmere
- Cytokrom P-450 enzymhæmmere
- Hormonantagonister
- Antifungale midler
- Steroidsyntesehæmmere
- 14-alfa-demethylasehæmmere
- Cytokrom P-450 CYP1A2-hæmmere
- Ciprofloxacin
- Itraconazol
Andre undersøgelses-id-numre
- MEI-007
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 Itraconazol
-
Alexandria UniversityRekrutteringTinea CapitisEgypten
-
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University of Maryland, BaltimoreAfsluttet
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Shandong Suncadia Medicine Co., Ltd.Afsluttet
-
University of Alabama at BirminghamWashington University School of Medicine; University of California, DavisAfsluttetInvasive svampeinfektionerForenede Stater, Panama
-
Urooj FatimaRekrutteringDermatofytose | Tinea CorporisPakistan
-
Multan Medical And Dental CollegeAfsluttetDermatofytose | Trichofytinfektion | Resistent dermatofytinfektionPakistan
-
Haisco Pharmaceutical Group Co., Ltd.Tilmelding efter invitation
-
AbbVieAktiv, ikke rekrutterendeHepatocellulært karcinom | Tredobbelt negativ brystkræft | Duktalt adenokarcinom i bugspytkirtlen | Esophageal pladecellekarcinom | Galdevejskræft | Hormonreceptor+/human epidermal vækstfaktorreceptor 2 negativ brystkræft | Hoved- og halspladecellekræft | Platinresistent højgradig epitelial ovariecancerForenede Stater, Australien, Israel, Japan, Puerto Rico, Sydkorea, Spanien, Taiwan