- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01900171
Phase I Study in Healthy Male Subjects Comparing QGC001 to Placebo
11. juli 2013 oppdatert av: 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.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
56
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Rueil-Malmaison, Frankrike, 92502
- Biotrial PARIS
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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:
- 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.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Trippel
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Eksperimentell: 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.
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Eksperimentell: 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.
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Eksperimentell: 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.
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Eksperimentell: 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.
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Eksperimentell: 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.
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Eksperimentell: 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.
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Eksperimentell: 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.
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Eksperimentell: 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.
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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.
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Inneholder magnesiumstearat, silika dental type, vannfri laktose
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Adverse events
Tidsramme: up to 11 days
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up to 11 days
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Blood pressure
Tidsramme: up to 11 days
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up to 11 days
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Heart rate
Tidsramme: up to 11 days
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up to 11 days
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Body temperature
Tidsramme: up to 11 days
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up to 11 days
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12-lead ECG
Tidsramme: up to 11 days
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up to 11 days
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Red blood cell count
Tidsramme: up to 11 days
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up to 11 days
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Haemoglobin
Tidsramme: up to 11 days
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up to 11 days
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Haematocrit
Tidsramme: up to 11 days
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up to 11 days
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White blood cell count with differential
Tidsramme: up to 11 days
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up to 11 days
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Platelet count
Tidsramme: up to 11 days
|
up to 11 days
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Plasma sodium
Tidsramme: up to 11 days
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up to 11 days
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Plasma potassium
Tidsramme: up to 11 days
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up to 11 days
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Plasma calcium
Tidsramme: up to 11 days
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up to 11 days
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Plasma total bilirubin
Tidsramme: up to 11 days
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up to 11 days
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Plasma conjugated bilirubin
Tidsramme: up to 11 days
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up to 11 days
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Plasma Aspartate Amino Transferase (ASAT)
Tidsramme: up to 11 days
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up to 11 days
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Plasma Alanine Amino Transferase (ALAT)
Tidsramme: up to 11 days
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up to 11 days
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Plasma Gamma Glutamyl Transferase (GGT)
Tidsramme: up to 11 days
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up to 11 days
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Plasma alkaline phosphatases
Tidsramme: up to 11 days
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up to 11 days
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Plasma total protein
Tidsramme: up to 11 days
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up to 11 days
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Plasma Creatine PhosphoKinase (CPK)
Tidsramme: up to 11 days
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up to 11 days
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Plasma creatinine
Tidsramme: up to 11 days
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up to 11 days
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Plasma glucose
Tidsramme: up to 11 days
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up to 11 days
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Plasma cholesterol
Tidsramme: up to 11 days
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up to 11 days
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Plasma triglycerides
Tidsramme: up to 11 days
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up to 11 days
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Urinary pH
Tidsramme: up to 11 days
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up to 11 days
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Urinary protein
Tidsramme: up to 11 days
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up to 11 days
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Urinary glucose
Tidsramme: up to 11 days
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up to 11 days
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Urinary leukocytes
Tidsramme: up to 11 days
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up to 11 days
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Urinary nitrites
Tidsramme: up to 11 days
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up to 11 days
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Urinary ketones
Tidsramme: up to 11 days
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up to 11 days
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Urinary blood
Tidsramme: up to 11 days
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up to 11 days
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
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Maximum observed plasma concentration (Cmax) of QGC001
Tidsramme: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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Time at which Cmax is observed (tmax) of QGC001
Tidsramme: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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Elimination rate constant (λz) of QGC001
Tidsramme: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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Terminal half-life (t1/2,z) of QGC001
Tidsramme: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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Area Under the Concentration-time curve (AUClast and AUC0-∞) of QGC001
Tidsramme: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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Maximum observed plasma concentration (MRCmax) of metabolic ratios
Tidsramme: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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Area Under the Concentration-time curve (MRAUC) of metabolic ratios
Tidsramme: H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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H0, H 0.5, H1, H1.5, H2, H3, H4, H5, H6, H9, H12, H24 and H48 post-dose
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Cumulative amount eliminated (Ae)
Tidsramme: H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
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H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
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Fraction recovered (Fe)
Tidsramme: H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
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H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
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Renal clearance (CLR)
Tidsramme: H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
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H-12 to H0 pre-dose and H0- H6, H6-H12 and H12-H24 post-dose
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Plasma renin
Tidsramme: H-1 pre-dose and H2, H4 and H9 post-dose
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Determination of renin in blood samples.
In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
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H-1 pre-dose and H2, H4 and H9 post-dose
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Plasma aldosterone
Tidsramme: H-1 pre-dose and H2, H4 and H9 post-dose
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Determination of aldosterone in blood samples.
In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
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H-1 pre-dose and H2, H4 and H9 post-dose
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Plasma cortisol
Tidsramme: H-1 pre-dose and H2, H4 and H9 post-dose
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Determination of cortisol in blood samples.
In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
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H-1 pre-dose and H2, H4 and H9 post-dose
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Plasma copeptin
Tidsramme: H-1 pre-dose and H2, H4 and H9 post-dose
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Determination of copeptin in blood samples (if possible, will be determined later).
In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
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H-1 pre-dose and H2, H4 and H9 post-dose
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Urinary aldosterone
Tidsramme: H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
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Aldosterone analysis in urine samples.
In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
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H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
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Urinary cortisol
Tidsramme: H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
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Cortisol analysis in urine samples.
In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
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H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
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Urinary creatinin
Tidsramme: H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
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Creatinin analysis in urine samples.
In dose groups 1 and 2, no pharmacodynamic evaluations will be done.
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H-12 to H0 pre-dose, H0-H6, H6-H12 and H12-H24 post-dose
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Publikasjoner og nyttige lenker
Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.
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. februar 2012
Primær fullføring (Faktiske)
1. mai 2012
Studiet fullført (Faktiske)
1. mai 2012
Datoer for studieregistrering
Først innsendt
26. juni 2013
Først innsendt som oppfylte QC-kriteriene
11. juli 2013
Først lagt ut (Anslag)
16. juli 2013
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
16. juli 2013
Siste oppdatering sendt inn som oppfylte QC-kriteriene
11. juli 2013
Sist bekreftet
1. juli 2013
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- QGC001/1QG1
Legemiddel- og utstyrsinformasjon, studiedokumenter
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Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
produkt produsert i og eksportert fra USA
Nei
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