- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03143725
Study to Compare Bioavailability of GLPG1972 Given as 2 Different Tablet Formulations Versus an Oral Solution
19. juni 2017 opdateret af: Galapagos NV
Open-label Study to Compare the Bioavailability of an Oral Wet Granulation Tablet of GLPG1972 Relative to an Oral Solution and to an Oral Direct Compression Tablet After Single-dose Intake in Healthy Subjects, and to Evaluate the Effect of Food on the Bioavailability of an Oral Wet Granulation Tablet.
This study is a Phase I, randomized, open-label, cross-over study with 4 single-dose treatments of GLPG1972 to compare the bioavailability of the oral wet granulation (WG) tablet relative to an oral solution and to the oral direct compression (DC) tablet after single dose intake in healthy male subjects and to evaluate the effect of food on the bioavailability of the WG oral tablet.
Studieoversigt
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
-
-
-
Antwerp, Belgien
- SGS Belgium Life Sciences
-
-
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 50 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Han
Beskrivelse
Inclusion Criteria:
- Male between 18 and 50 years of age, inclusive,
- A body mass index (BMI) between 18-30 kg/m², inclusive, weight of at least 50 kg.
- Judged by the investigator to be in good health based upon the results of a medical history, physical examination, vital signs, 12-lead ECG, and laboratory findings.
- Discontinuation of all medications except occasional paracetamol at least 2 weeks or 5 half-lives prior to the first study drug administration.
- Non-smokers and not using any nicotine-containing products.
- Negative urine drug screen and alcohol breath test.
- Current sexually active male agrees to use adequate contraception
- Willing to consume a non-vegetarian high-fat and high-calorie breakfast
- Able and willing to sign the ICF
Exclusion Criteria:
- Known hypersensitivity to study drug ingredients or a significant allergic reaction to any drug
- Positive serology for hepatitis B virus surface antigen (HBsAg) or hepatitis C virus (HCV) or any history of hepatitis from any cause with the exception of hepatitis A.
- History of or a current immunosuppressive condition
- Symptoms of clinically significant illness in the 3 months before the initial study drug administration.
- History of malignancy within the past 5 years
- Clinically relevant abnormalities detected on ECG regarding either rhythm or conduction (e.g. QTcF >450 msec, or a known long QT syndrome).
- Presence of abnormal liver function
- Renal function with an estimated creatinine clearance <80 ml/min based on the Cockcroft-Gault formula.
- Presence of any condition known to interfere with absorption, distribution, metabolism or excretion of drugs.
- Clinically relevant abnormalities detected on "vital signs"
- Dietary requirements precluding participation.
- Significant blood loss including blood donation or had a transfusion of any blood product within 12 weeks
- Hemoglobin level <7.5 mmol/L (12 g/dL).
- Active drug or alcohol abuse within 2 years prior to the initial study drug administration.
- Current (2 weeks before screening) and planned uninterrupted consumption of large quantities (> 6 cups) of coffee
- Administration of an injectable drug within 30 days prior to the initial study drug administration.
- Concurrent participation, or participation in a drug/device study within 8 weeks or 5 half-lives of the drug or within 6 months for biologicals
- Investigator or any sub-investigator, research assistant, pharmacist, study coordinator, or other staff
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: Treatment A
GLPG1972 oral solution after overnight fast
|
Oral administration of GLPG1972 in four different treatment conditions (Treatments A throug D)
|
|
Eksperimentel: Treatment B
GLPG1972 oral DC tablet after breakfast
|
Oral administration of GLPG1972 in four different treatment conditions (Treatments A throug D)
|
|
Eksperimentel: Treatment C
GLPG1972 oral WG tablet after overnight fast
|
Oral administration of GLPG1972 in four different treatment conditions (Treatments A throug D)
|
|
Eksperimentel: Treatment D
GLPG1972 oral WG tablet after breakfast
|
Oral administration of GLPG1972 in four different treatment conditions (Treatments A throug D)
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Assessment of the maximum observed plasma concentration of GLPG1972 after single oral doses
Tidsramme: on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
|
Determine bioavailability of GLPG1972 by assessing PK parameters
|
on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
|
|
Assessment of plasma concentration of GLPG1972 24hrs post-dose after single oral doses
Tidsramme: At 24 hours post dose
|
Determine bioavailability of GLPG1972 by assessing PK parameters
|
At 24 hours post dose
|
|
Assessment of time to achieve the maximal plasma concentration of GLPG1972 after single oral doses
Tidsramme: on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
|
Determine bioavailability of GLPG1972 by assessing PK parameters
|
on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
|
|
Assessment of the last quantifiable plasma concentration of GLPG1972 after single oral doses
Tidsramme: on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
|
Determine bioavailability of GLPG1972 by assessing PK parameters
|
on day 1 pre-dose and at 0.5, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 12, 16, 24 and 48 hours post doses
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
the number of subjects with adverse events
Tidsramme: at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
|
To assess safety and tolerability of GLPG1972 given orally
|
at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
|
|
the number of subjects with abnormal vital signs
Tidsramme: at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
|
To assess safety and tolerability of GLPG1972 given orally
|
at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
|
|
the number of subjects with abnormal ECG
Tidsramme: at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
|
To assess safety and tolerability of GLPG1972 given orally
|
at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
|
|
the number of subjects with abnormal laboratory assessments
Tidsramme: at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
|
To assess safety and tolerability of GLPG1972 given orally
|
at screening, pre-dose at date 1 and post-dose at 24 and 48 hours
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Studieleder: Ann Fieuw, MD MSc, Galapagos NV
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 (Faktiske)
14. april 2017
Primær færdiggørelse (Faktiske)
6. juni 2017
Studieafslutning (Faktiske)
6. juni 2017
Datoer for studieregistrering
Først indsendt
4. maj 2017
Først indsendt, der opfyldte QC-kriterier
4. maj 2017
Først opslået (Faktiske)
8. maj 2017
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
20. juni 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
19. juni 2017
Sidst verificeret
1. juni 2017
Mere information
Begreber relateret til denne undersøgelse
Andre undersøgelses-id-numre
- GLPG1972-CL-105
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
UBESLUTET
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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 GLPG1972
-
Galapagos NVAfsluttet
-
Galapagos NVInstitut de Recherches Internationales ServierAfsluttet
-
Galapagos NVPRA Health SciencesAfsluttet
-
Galapagos NVAfsluttet