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Relative Bioavailability and Food Effect Study of IX-01 Capsules in Healthy Men

5. august 2020 oppdatert av: Ixchelsis Limited

A Randomised, Single-dose, 3-way Crossover Study to Evaluate the Relative Bioavailability of the IX-01 Capsule Formulation Compared With the IX-01 Aqueous Dispersion Formulation, and the Effect of Food on the IX-01 Capsule Formulation, in Healthy Male Subjects

The purpose of this study is to compare the absorption and blood levels of IX-01 when given as a capsule compared to liquid form, and how food affects the absorption in healthy men.

Studieoversikt

Status

Fullført

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Faktiske)

12

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • London, Storbritannia
        • Hammersmith Medicines Research

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

Nei

Kjønn som er kvalifisert for studier

Mann

Beskrivelse

Inclusion Criteria:

  • A body mass index (Quetelet index) in the range 18-30 kilograms/meters squared (kg/m2)
  • Body Mass Index = weight [kg] divided by (height [m])2
  • Total body weight greater than (>)50 kg at screening
  • Ability to communicate satisfactorily with the investigator and to participate in, and comply with the requirements of, the entire trial
  • Participants and their partners must be willing to use adequate forms of contraception and to comply with the contraception requirements during the trial and for 4 months after the last dose of medication
  • Willingness to give written consent to have data entered into The Over Volunteering Prevention System

Exclusion Criteria:

  • Clinically relevant abnormal history, physical findings, ECG, or laboratory values at the pre-trial screening assessment, including:

    • Lipid and/or liver function test results >1.25 x Upper Limit of Normal (ULN) or other clinical laboratory blood biochemistry test results outside the normal reference range unless discussed and approved by sponsor
    • International normalised ratio (INR) of >1.2 or a platelet count < 150 x 109/Liter
    • History of unexplained syncope
    • Family history of unexplained sudden death, or sudden death due to long QT syndrome
    • Fridericia Correction Formula (QTcF) interval >450 milliseconds (msec) at screening
    • Bundle branch block and other conduction abnormalities, other than mild first degree atrio-ventricular block
    • Irregular rhythms other than sinus arrhythmia or occasional supraventricular ectopic beats
    • T-wave configuration of insufficient quality for determination of QT interval, as assessed by the investigator
  • Presence of acute or chronic illness or history of chronic illness sufficient to invalidate participation in the trial
  • Impaired gastrointestinal, endocrine, thyroid, hepatic, cardiovascular, respiratory, haematological, renal or neurological function, diabetes mellitus, coronary heart disease, or history of any psychotic mental illness
  • Surgery (for example (e.g.) stomach bypass) or medical condition that might affect absorption, metabolism or elimination of medicines
  • Any skin condition, abnormality of the lumbar spine, medical or surgical condition that would preclude lumbar puncture (e.g. coagulopathy, local or systemic infection, left ventricular outflow obstruction, aortic stenosis, previous back surgery)
  • Presence or history of severe adverse reaction to any drug
  • Use of any prescription or over-the-counter medicine during the 14 days before the first dose of trial medication, or intention to use any medicine during the trial, with the exception of short courses of medication considered by the investigator not to interfere with the safety of the participant or the integrity of the trial data (such as acetaminophen (paracetamol))
  • Current use of any herbal remedy or nutritional supplement, or intention to use any such product during the study
  • Participation in another clinical trial of a new chemical entity or a prescription medicine within the previous 3 months.
  • Previous participation in this trial or any other clinical trial of an oxytocin receptor antagonist
  • Presence or history of drug or alcohol abuse, or intake of more than 21 units of alcohol weekly or more than 5 cigarettes daily
  • Blood pressure and heart rate in supine position at the screening examination outside the ranges 100-130 millimeters of mercury (mm Hg) systolic, 60-90 mm Hg diastolic; heart rate 50-100 beats/minute. Measurements must be made in duplicate, and all values must fall within the acceptable ranges
  • Possibility that the participant will not cooperate with the requirements of the protocol
  • Evidence of drug abuse on urine testing
  • Positive test for hepatitis B, hepatitis C, Human Immunodeficiency Virus 1 (HIV1) or Human Immunodeficiency Virus 2 (HIV2)
  • Loss of more than 400 mL blood during the 3 months before the trial, e.g. as a blood donor
  • Objection by General Practitioner (GP), on medical grounds, to participant entering trial
  • Employee of the investigator site or any company involved in sponsoring, organizing or conducting the trial, or immediate family of the employee

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: Crossover-oppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: IX-01 Capsule while Fasting
Singe oral dose of 800 milligrams of IX-01 as a capsule, while fasting, in 1 of 3 treatment periods
Eksperimentell: IX-01 Aqueous Dispersion while Fasting
Single oral dose of 800 milligrams IX-01 as an aqueous dispersion, while fasting in 1 of 3 treatment periods
Eksperimentell: IX-01 Capsule after Food
Single oral dose of 800 milligrams IX-01 as a capsule, after food, in 1 of 3 treatment periods

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Relative Bioavailability (Frel) of a Capsule Compared to a Liquid Formulation of IX-01 While Fasting, as Calculated by a Ratio of Area Under the Plasma Concentration Time Curve From Time 0 to Infinity
Tidsramme: Pre-dose up to 96 hours post dose
Pre-dose up to 96 hours post dose
Relative Bioavailability (Frel) of a Capsule Formulation of IX-01 in the Fed State Compared to the Fasted State, as Calculated by a Ratio of Area Under the Plasma Concentration Time Curve From Time 0 to Infinity
Tidsramme: Pre-dose up to 96 hours post dose
Pre-dose up to 96 hours post dose
Relative Bioavailability (Frel) of a Capsule Compared With a Liquid Formulation of IX-01 While Fasting, as Calculated by a Ratio of Peak Plasma Concentrations
Tidsramme: Pre-dose up to 96 hours post dose
Pre-dose up to 96 hours post dose
Relative Bioavailability (Frel) of a Capsule Formulation of IX-01 in a Fed State Compared to a Fasted State, as Calculated by a Ratio of Peak Plasma Concentrations
Tidsramme: Pre-dose up to 96 hours post dose
Pre-dose up to 96 hours post dose
Area Under the Plasma Concentration Time Curve From Time 0 to Infinity, Following a Single Dose of IX-01
Tidsramme: Pre-dose and up to 96 hours post dose
Pre-dose and up to 96 hours post dose
Peak Plasma Concentration (Cmax) of IX-01
Tidsramme: Pre-dose and up to 96 hours post dose
Pre-dose and up to 96 hours post dose
Time to Peak Plasma Concentration (Tmax) of IX-01
Tidsramme: Pre-dose up to 96 hours post dose
Pre-dose up to 96 hours post dose
Elimination Half Life (t1/2) of IX-01
Tidsramme: Pre-dose up to 96 hours post dose
Pre-dose up to 96 hours post dose
Elimination Rate Constant (Kel) of IX-01
Tidsramme: Pre-dose up to 96 hours post last dose
Pre-dose up to 96 hours post last dose
Area Under the Plasma Concentration Time Curve From Time 0 to the Time of the Last Measurable Sample of IX-01
Tidsramme: Pre-dose to the time of the last measurable sample
Pre-dose to the time of the last measurable sample
Concentration of IX-01 in Cerebrospinal Fluid (CSF) After a Single Dose of the Liquid Formulation of IX-01
Tidsramme: 1, 2, 4 and 6 hours after dosing
Listed by time point of 1, 2, 4, 6 hours post dose
1, 2, 4 and 6 hours after dosing

Sekundære resultatmål

Resultatmål
Tidsramme
Number of Participants With One or More Drug-Related Adverse Events (AEs) or Any Serious AEs
Tidsramme: Baseline to study completion (approximately 6 weeks)
Baseline to study completion (approximately 6 weeks)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Studieleder: Email: Ixchelsis@Choruspharma.com, Ixchelsis Limited

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 2014

Primær fullføring (Faktiske)

1. juni 2014

Studiet fullført (Faktiske)

1. juni 2014

Datoer for studieregistrering

Først innsendt

12. mai 2014

Først innsendt som oppfylte QC-kriteriene

13. mai 2014

Først lagt ut (Anslag)

15. mai 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

20. august 2020

Siste oppdatering sendt inn som oppfylte QC-kriteriene

5. august 2020

Sist bekreftet

1. august 2020

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

  • IX-0102

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. .

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