- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02564861
Multiple Dose Study of D1971a in Healthy Volunteers
27. april 2017 opdateret af: 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.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
25
Fase
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
-
London, Det Forenede Kongerige
- Mammersmith Medicines Research Ltd.
-
-
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 65 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
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.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Grundvidenskab
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 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
|
|
Eksperimentel: 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
|
|
Eksperimentel: 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
|
|
Eksperimentel: Pooled placebo
Participants in Cohort 1, 2 or 3 who receive matching DS-1971a Placebo
|
Placebo matching DS-1971a suspension
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Number of participants with at least one Treatment Emergent Adverse Event (TEAEs)
Tidsramme: 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
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Cmax of DS-1971a
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: Day 1 and Day 14
|
AUC measures include AUCtau, AUC0-24, AUClast, AUC0-inf
|
Day 1 and Day 14
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
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. september 2015
Primær færdiggørelse (Faktiske)
1. december 2015
Studieafslutning (Faktiske)
1. december 2015
Datoer for studieregistrering
Først indsendt
28. september 2015
Først indsendt, der opfyldte QC-kriterier
29. september 2015
Først opslået (Skøn)
1. oktober 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
28. april 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
27. april 2017
Sidst verificeret
1. april 2017
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- DS1971-A-E106
- 2015-002885-22 (EudraCT nummer)
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 DS-1971a
-
Daiichi Sankyo, Inc.AfsluttetSund og raskDet Forenede Kongerige
-
Daiichi Sankyo, Inc.AfsluttetSund og raskDet Forenede Kongerige
-
Daiichi Sankyo, Inc.Afsluttet
-
Daiichi SankyoRekrutteringSarkom | Faste tumorerForenede Stater, Korea, Republikken, Holland, Belgien, Frankrig
-
Daiichi Sankyo Co., Ltd.Aktiv, ikke rekrutterende
-
Daiichi Sankyo Co., Ltd.AfsluttetAvanceret solid tumorForenede Stater, Japan
-
Hospital St. Joseph, Marseille, FranceAfsluttetPancreatitis, kroniskFrankrig
-
M.D. Anderson Cancer CenterDaiichi Sankyo UK Ltd.Afsluttet
-
Daiichi Sankyo, Inc.Hammersmith Medicines ResearchAfsluttetSund og raskDet Forenede Kongerige
-
Sierra Medical Ltd.Queen Alexandra HospitalRekruttering