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Multiple Dose Study of D1971a in Healthy Volunteers

27 avril 2017 mis à jour par: Daiichi Sankyo, Inc.

A Phase I, Double-Blind, Randomised, Placebo Controlled, Multiple-Dose Study to Assess Safety, Tolerability and Pharmacokinetics of DS-1971a in Healthy Male and Female Subjects

This is a randomised, double-blind, placebo-controlled multiple dose study designed to explore the safety, tolerability and PK of DS-1971a following oral administration over 14 days to healthy male and female subjects. Each participant receives lidocaine as a local anaesthetic before inserting the intravenous cannula.

Aperçu de l'étude

Statut

Complété

Les conditions

Description détaillée

Within strictly defined limits, the protocol permits the dose escalation committee to amend the dose escalation rules, doses proposed in the study protocol and to change the timing of or to add additional assessments following review of the safety, tolerability and plasma DS-1971a concentration data. The decisions to change the doses will be documented in the minutes of the dose escalation committee.

Type d'étude

Interventionnel

Inscription (Réel)

25

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • London, Royaume-Uni
        • Mammersmith Medicines Research Ltd.

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 65 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Healthy male and female subjects aged 18 years to 65 years.
  • A body mass index (BMI) in the range 18 kg/m2 to 30 kg/m2, inclusive, and weighing between 50 kg and 100 kg, inclusive at screening. BMI is calculated as weight [kg]/(height [m])2.
  • Female subjects must be of non-childbearing potential as follows:

    • Must be postmenopausal (the last menstrual period was at least 12 months before Screening, and a follicle stimulating hormone [FSH] test at Screening confirms postmenopausal status); or
    • Must be surgically sterile having undergone hysterectomy, bilateral oophorectomy, bilateral salpingectomy and/or bilateral tubal ligation.
  • Willing to comply with all study restrictions, including the use of contraception, concomitant medication, and dietary and lifestyle restrictions.
  • Sufficient intelligence to understand the nature of the study and any hazards of participating in it. Ability to communicate satisfactorily with the Investigator and to participate in, and comply with requirements of, the entire study.
  • Have given written consent to participate in the study after reading the ICF, and after having the opportunity to discuss the study with the Investigator or his delegate.
  • Have given written consent to have his/her data entered into The Over volunteering Prevention System.

Exclusion Criteria:

  • Clinically relevant abnormal history, physical findings, ECG findings, or laboratory values that could interfere with the objectives of the study or compromise the safety of the subject.
  • Presence or history of acute or chronic illness, including (but not limited to) liver or kidney disease, hypertension, seizures, or any known impairment of endocrine, or other specific body-organ dysfunction.
  • History of serious reaction to any medicine.
  • Presence or history of malignant disease.
  • Acute or chronic infectious disease, including human immunodeficiency virus (HIV), hepatitis B virus (HBV) or C virus (HCV) infection.
  • Surgery (eg, stomach bypass) or medical condition that might affect how the body handles or absorbs medicines.
  • Significant illness within 4 weeks before the first dose of study medication.
  • Participation in another clinical study of a new chemical entity or a prescription medicine within the previous 3 months, or unwilling to abstain from participating in other clinical trials during the study and for 3 months after receipt of study medication.
  • Blood pressure (BP) and heart rate in semi-supine position at the Screening examination outside the ranges 90 mmHg to 140 mmHg systolic, 40 mmHg to 90 mmHg diastolic; heart rate < 40 beats/min to > 100 beats/min. Subjects with Stage 1 hypertension (systolic 140 mmHg to 160 mmHg; diastolic 90 mmHg to 100 mmHg) may be enrolled provided they do not have evidence of end-organ damage, diabetes or a 10 year cardiovascular risk > 20%.
  • Abnormal ECG waveform morphology at Screening that would preclude accurate measurement of the uncorrected QT interval (QT) duration.
  • QT interval for heart rate corrected using QTcF interval duration > 430 ms for men or > 450 ms for women, obtained as an average from the measurements on duplicate Screening ECGs over a brief recording period.
  • Estimated glomerular filtration rate (eGFR) < 80 mL/min/1.73m2 (based on Modification of Diet in Renal Disease [MDRD] equation) or an absolute creatinine value outside the normal range.
  • Use of any prescription or over the counter (OTC) medications, or herbal remedies (such as St John's wort), known to be strong inhibitors or strong inducers of cytochrome (CYP) enzymes (also known as CYP P450 enzymes) during the 30 days before the first dose of study medication; use of any other prescription or OTC medicine (with the exception of acetaminophen (paracetamol)), including dietary supplements or herbal remedies, during the 7 days before the dose of study medication.
  • Pregnant or breastfeeding women.
  • Consumption of certain foods or beverages before the first dose and throughout the study period.
  • Loss of more than 400 mL blood or donation of blood, plasma, platelets, or any other blood components during the 3 months before the first dose of study medication, or unwilling to abstain from doing so during the study and for 3 months after receipt of study medication.
  • Abuse of drugs or alcohol during the 2 years before the first dose of study medication, or intake of more than 21 units of alcohol weekly for male subjects and 14 units of alcohol weekly for female subjects.
  • Use of tobacco products or nicotine-containing products during the 3 months before the first dose of study medication and during the study.
  • Evidence of drug or alcohol abuse at screening or admission.
  • Likely possibility that the volunteer will not cooperate with the requirements of the protocol.
  • Objection by General Practitioner (GP) to the volunteer entering the study.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Quadruple

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: DS-1971a (Low Dose)
Participants in Cohort 1 who receive a low dose of DS 1971a in an oral suspension
DS 1971a is supplied as a powder or crystals and will be given as an oral suspension
Expérimental: DS-1971a (Mid dose)
Participants in Cohort 2 who receive a mid dose of DS 1971a in an oral suspension
DS 1971a is supplied as a powder or crystals and will be given as an oral suspension
Expérimental: DS-1971a (High dose)
Participants in Cohort 3 who receive a high dose of DS 1971a in an oral suspension
DS 1971a is supplied as a powder or crystals and will be given as an oral suspension
Expérimental: Pooled placebo
Participants in Cohort 1, 2 or 3 who receive matching DS-1971a Placebo
Placebo matching DS-1971a suspension

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Number of participants with at least one Treatment Emergent Adverse Event (TEAEs)
Délai: 14 days
TEAEs are adverse events that began or got worse after treatment began. Clinically significant changes in laboratory tests and/or physical examinations are considered adverse events.
14 days

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Cmax of DS-1971a
Délai: Day 1 and Day 14
Cmax is the highest concentration of the drug in the blood
Day 1 and Day 14
Tmax of DS-1971a
Délai: Day 1 and Day 14
Tmax is the time it takes for Cmax to be reached
Day 1 and Day 14
Area Under Curve at steady state (AUCtau) of DS-1971a
Délai: Day 1 and Day 14
AUCtau is the area under the plasma concentration-time curve at steady state. In pharmacokinetics, steady state refers to the situation where the overall intake of a drug is about even with the rate it is being eliminated from the body.
Day 1 and Day 14
Area under the Curve (additional measures) for DS-1971a
Délai: Day 1 and Day 14
Additional AUC measures include AUC0-24 (to 24 hours), AUClast (to the last observable measure), AUC0-inf (to infinity), and AUCextr (from AUClast to infinity)
Day 1 and Day 14
Tmax of DS-1971a metabolites M1 and M2
Délai: Day 1 and Day 14
Tmax of metabolites M1 and M2 characterized by Tmax
Day 1 and Day 14
Cmax of DS-1971a metabolites M1 and M2
Délai: Day 1 and Day 14
Cmax of metabolites M1 and M2 characterized by Cmax
Day 1 and Day 14
AUC of DS-1971a metabolites M1 and M2
Délai: Day 1 and Day 14
AUC measures include AUCtau, AUC0-24, AUClast, AUC0-inf
Day 1 and Day 14

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 septembre 2015

Achèvement primaire (Réel)

1 décembre 2015

Achèvement de l'étude (Réel)

1 décembre 2015

Dates d'inscription aux études

Première soumission

28 septembre 2015

Première soumission répondant aux critères de contrôle qualité

29 septembre 2015

Première publication (Estimation)

1 octobre 2015

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

28 avril 2017

Dernière mise à jour soumise répondant aux critères de contrôle qualité

27 avril 2017

Dernière vérification

1 avril 2017

Plus d'information

Termes liés à cette étude

Mots clés

Autres numéros d'identification d'étude

  • DS1971-A-E106
  • 2015-002885-22 (Numéro EudraCT)

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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