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Phase I Study in Healthy Male Subjects Comparing QGC001 to Placebo

11. Juli 2013 aktualisiert von: Quantum Genomics SA

A Phase I, Double-blind, Placebo-controlled, Ascending Single-dose, Safety, Tolerability and Pharmacokinetic Study of QGC001 in Healthy Male Subjects.

QGC001/1QG1 is a Phase I "first time in man" study aiming to determine the overall safety and tolerability of single ascending oral doses of QGC001 in healthy male subjects compared to placebo, as well as the pharmacokinetics of QGC001 and its metabolite EC33 and the pharmacodynamic properties of QGC001 (effects on the renin-angiotensin-aldosterone system, blood pressure and heart rate) in healthy male subjects.

Studienübersicht

Status

Abgeschlossen

Bedingungen

Intervention / Behandlung

Studientyp

Interventionell

Einschreibung (Tatsächlich)

56

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienorte

      • Rueil-Malmaison, Frankreich, 92502
        • Biotrial PARIS

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 45 Jahre (Erwachsene)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Männlich

Beschreibung

Inclusion Criteria:

  • Caucasian, male healthy subjects of 18 to 45 years of age.
  • Body weight ≥50 kg, with a body mass index calculated as weight in kg/(height in m2) from 18 to 27 kg/m2 at screening.
  • Subjects will sign and date an informed consent form before any study-specific screening procedure is performed.
  • Healthy, as determined by the investigator on the basis of medical history, physical examination findings, clinical laboratory test results, vital sign measurements, and digital 12 lead ECG readings.
  • Non-smoker or smoker of fewer than 5 cigarettes per day as determined by history. Must be able to abstain from smoking during the inpatient stay.
  • Have a high probability for compliance with and completion of the study.

Exclusion Criteria:

  • Any significant cardiovascular, hepatic, renal, respiratory, gastrointestinal, endocrine, immunologic, dermatological, haematological, neurologic, psychiatric disease or history of any clinically important drug allergy.
  • Acute disease state within 7 days before study day 1.
  • History of drug abuse within 1 year before study day 1.
  • History of alcoholism within 1 year before day 1. Consumption of more than 50 g of ethanol per day.
  • Positive serologic findings for human immunodeficiency virus antibodies, hepatitis B surface antigen, and/or hepatitis C virus antibodies.
  • Positive findings of urine drug screen (e.g., amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine, methadone, opiates, MDMA)
  • History of any clinically important drug allergy.
  • Prohibited Treatments: use of any investigational drug within 90 days or prescription drug within 30 days before investigational medical product administration.
  • Consumption of any caffeine-containing products in excess of 6 cups per day (or equivalent), of grapefruit, grapefruit-containing products, or alcoholic beverages within 24 hours before study day 1.
  • Use of any over-the-counter drugs including herbal supplements (except for the occasional use of acetaminophen [paracetamol], aspirin and vitamins ≤100% recommended daily allowance) within 7 days before investigational medicinal product administration.
  • Donation of blood (i.e. 450 ml) within 90 days before study day 1.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Verdreifachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: 10 mg of QGC001
Each dose of QGC001 was administered orally with 100 mL of sterile water for irrigation at 08:00 in the morning of Day 1.
Experimental: 50 mg of QGC001
Each dose of QGC001 was administered orally with 100 mL of sterile water for irrigation at 08:00 in the morning of Day 1.
Experimental: 125 mg of QGC001
Each dose of QGC001 was administered orally with 100 mL of sterile water for irrigation at 08:00 in the morning of Day 1.
Experimental: 250 mg of QGC001
Each dose of QGC001 was administered orally with 100 mL of sterile water for irrigation at 08:00 in the morning of Day 1.
Experimental: 500 mg of QGC001
Each dose of QGC001 was administered orally with 100 mL of sterile water for irrigation at 08:00 in the morning of Day 1.
Experimental: 750 mg of QGC001
Each dose of QGC001 was administered orally with 100 mL of sterile water for irrigation at 08:00 in the morning of Day 1.
Experimental: 1,000 mg of QGC001
Each dose of QGC001 was administered orally with 100 mL of sterile water for irrigation at 08:00 in the morning of Day 1.
Experimental: 1,250 mg of QGC001
Each dose of QGC001 was administered orally with 100 mL of sterile water for irrigation at 08:00 in the morning of Day 1.
Placebo-Komparator: Placebo
The placebo was administered orally with 100 mL of sterile water for irrigation at 08:00 in the morning of Day 1.
Enthält Magnesiumstearat, Silica Dental, wasserfreie Laktose

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Adverse events
Zeitfenster: up to 11 days
up to 11 days
Blood pressure
Zeitfenster: up to 11 days
up to 11 days
Heart rate
Zeitfenster: up to 11 days
up to 11 days
Body temperature
Zeitfenster: up to 11 days
up to 11 days
12-lead ECG
Zeitfenster: up to 11 days
up to 11 days
Red blood cell count
Zeitfenster: up to 11 days
up to 11 days
Haemoglobin
Zeitfenster: up to 11 days
up to 11 days
Haematocrit
Zeitfenster: up to 11 days
up to 11 days
White blood cell count with differential
Zeitfenster: up to 11 days
up to 11 days
Platelet count
Zeitfenster: up to 11 days
up to 11 days
Plasma sodium
Zeitfenster: up to 11 days
up to 11 days
Plasma potassium
Zeitfenster: up to 11 days
up to 11 days
Plasma calcium
Zeitfenster: up to 11 days
up to 11 days
Plasma total bilirubin
Zeitfenster: up to 11 days
up to 11 days
Plasma conjugated bilirubin
Zeitfenster: up to 11 days
up to 11 days
Plasma Aspartate Amino Transferase (ASAT)
Zeitfenster: up to 11 days
up to 11 days
Plasma Alanine Amino Transferase (ALAT)
Zeitfenster: up to 11 days
up to 11 days
Plasma Gamma Glutamyl Transferase (GGT)
Zeitfenster: up to 11 days
up to 11 days
Plasma alkaline phosphatases
Zeitfenster: up to 11 days
up to 11 days
Plasma total protein
Zeitfenster: up to 11 days
up to 11 days
Plasma Creatine PhosphoKinase (CPK)
Zeitfenster: up to 11 days
up to 11 days
Plasma creatinine
Zeitfenster: up to 11 days
up to 11 days
Plasma glucose
Zeitfenster: up to 11 days
up to 11 days
Plasma cholesterol
Zeitfenster: up to 11 days
up to 11 days
Plasma triglycerides
Zeitfenster: up to 11 days
up to 11 days
Urinary pH
Zeitfenster: up to 11 days
up to 11 days
Urinary protein
Zeitfenster: up to 11 days
up to 11 days
Urinary glucose
Zeitfenster: up to 11 days
up to 11 days
Urinary leukocytes
Zeitfenster: up to 11 days
up to 11 days
Urinary nitrites
Zeitfenster: up to 11 days
up to 11 days
Urinary ketones
Zeitfenster: up to 11 days
up to 11 days
Urinary blood
Zeitfenster: up to 11 days
up to 11 days

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Maximum observed plasma concentration (Cmax) of QGC001
Zeitfenster: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
Time at which Cmax is observed (tmax) of QGC001
Zeitfenster: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
Elimination rate constant (λz) of QGC001
Zeitfenster: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
Terminal half-life (t1/2,z) of QGC001
Zeitfenster: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
Area Under the Concentration-time curve (AUClast and AUC0-∞) of QGC001
Zeitfenster: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
Maximum observed plasma concentration (MRCmax) of metabolic ratios
Zeitfenster: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
Area Under the Concentration-time curve (MRAUC) of metabolic ratios
Zeitfenster: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
Cumulative amount eliminated (Ae)
Zeitfenster: H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
Fraction recovered (Fe)
Zeitfenster: H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
Renal clearance (CLR)
Zeitfenster: H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
Plasma renin
Zeitfenster: H-1 pre-dose and H2, H4 and H9 post-dose
Determination of renin in blood samples. In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
H-1 pre-dose and H2, H4 and H9 post-dose
Plasma aldosterone
Zeitfenster: H-1 pre-dose and H2, H4 and H9 post-dose
Determination of aldosterone in blood samples. In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
H-1 pre-dose and H2, H4 and H9 post-dose
Plasma cortisol
Zeitfenster: H-1 pre-dose and H2, H4 and H9 post-dose
Determination of cortisol in blood samples. In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
H-1 pre-dose and H2, H4 and H9 post-dose
Plasma copeptin
Zeitfenster: H-1 pre-dose and H2, H4 and H9 post-dose
Determination of copeptin in blood samples (if possible, will be determined later). In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
H-1 pre-dose and H2, H4 and H9 post-dose
Urinary aldosterone
Zeitfenster: H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
Aldosterone analysis in urine samples. In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
Urinary cortisol
Zeitfenster: H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
Cortisol analysis in urine samples. In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
Urinary creatinin
Zeitfenster: H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
Creatinin analysis in urine samples. In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Februar 2012

Primärer Abschluss (Tatsächlich)

1. Mai 2012

Studienabschluss (Tatsächlich)

1. Mai 2012

Studienanmeldedaten

Zuerst eingereicht

26. Juni 2013

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

11. Juli 2013

Zuerst gepostet (Schätzen)

16. Juli 2013

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

16. Juli 2013

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

11. Juli 2013

Zuletzt verifiziert

1. Juli 2013

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • QGC001/1QG1

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

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