Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Pharmacodynamics, Preliminary Pharmacokinetics and Tolerability of BIBB 1464 (Tablet) in Hyperlipemic Healthy Male Subjects

28. august 2014 opdateret af: Boehringer Ingelheim

Pharmacodynamics, Preliminary Pharmacokinetics and Tolerability After Multiple Oral Doses of 0.25 mg, 0.5 mg and 1 mg o.d. BIBB 1464 (Tablet) or Pravastatin 20 mg Over 2 Weeks in Hyperlipemic Healthy Male Subjects (Parallel Group Comparison, Randomized, Placebo Controlled, Partly Double Blind [Pravastatin Open])

Lipid lowering effect, investigation of pharmacodynamics (inhibition of oxidosqualene cyclase, monoepoxysqualene (MES) as marker), safety / tolerability and preliminary pharmacokinetics

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

100

Fase

  • Fase 1

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

Han

Beskrivelse

Inclusion Criteria:

  • Healthy male Caucasian subjects as determined by results of screening
  • Written informed consent in accordance with GCP and local legislation given
  • Age >= 18 and <= 65 years
  • Broca >= - 20% and <= + 30%
  • LDL-cholesterol level >= 3.3 mmol/L at pre-screening and at the two screening visits

Exclusion Criteria:

  • Any finding of the medical examination. (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
  • Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal (including thyroid) disorder
  • Surgery of the gastro-intestinal tract (except appendectomy)
  • Disease of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
  • History or orthostatic hypotension, fainting spells or blackouts
  • Chronic or relevant acute infections
  • History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged the investigator
  • Intake of drugs with a long half-life (> 24 hours) (<= 1 month prior to administration or during the trial)
  • Use of any drugs which might influence the result of the trial (<= 10 days prior to administration or during the trial)
  • Participation in another trial with an investigational drug (<= 2 month prior to administration or during the trial)
  • Smoker (> 10 cigarettes or > 3 cigars or >3 pipes/day)
  • Inability to refrain from smoking during the period of the study
  • Alcohol abuse (>60/g/day)
  • Drug abuse
  • Blood donation (>400ml <=1 month prior to administration)
  • Excessive physical activities (<=5 days prior to administration)
  • Any laboratory value outside the normal range of clinical relevance
  • LDL - cholesterol screening measurements day -1 and day -7 the different between these two values exceed 12% of the higher dose
  • subjects who are vegetarian

Eye-lens

  • Cataract extraction in one or both eyes deemed likely within 2 years ("senile", non-idiopathic will not automatically exclude patients from participation)
  • Lens Opacities Classification System (LOCS) III grade >3.0 (for nuclear opalescence or cortical grad) >0.5 (for posterior sub capsular grad)
  • Log MAR Bailey-Lovie visual acuity >0.5
  • Corneal or conjunctival problems which would preclude lens photography
  • Shallow anterior chamber with risk of angle-closure glaucoma
  • Pupil will not dilate to at least 6 mm
  • Visually significant fundus pathology in clinician's judgment
  • Amblyopia, optic nerve disease, iritis, history of eye surgery, argon or YAG laser, major eye trauma, extended use (daily for >3 month) of ocular or systemic corticosteroid treatment , use of anticoagulants, or glaucoma therapy, or participation in another clinical trial investigation an anti-cataract or cataractogenic formulation within the last year

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Placebo
Aktiv komparator: Pravastatin
Eksperimentel: BIBB 1464 MS low dose
Eksperimentel: BIBB 1464 MS medium dose
Eksperimentel: BIBB 1464 MS high dose

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Percentage change of LDL plasma cholesterol
Tidsramme: baseline, 2 weeks
baseline, 2 weeks
Percentage change of total plasma cholesterol
Tidsramme: baseline, 2 weeks
baseline, 2 weeks

Sekundære resultatmål

Resultatmål
Tidsramme
Percentage change in lipid profile
Tidsramme: baseline, 1 week
baseline, 1 week
Number of patients with adverse events
Tidsramme: Up to day 42
Up to day 42
Number of patients with clinical significant findings in eye lens opacification
Tidsramme: Up to day 42
Up to day 42
Number of patients with clinical significant findings in laboratory parameters
Tidsramme: Up to day 28
Up to day 28
Number of patients with clinical significant findings in electrocardiogram (ECG)
Tidsramme: Up to day 28
Up to day 28
Number of patients with clinical significant findings in physical examination
Tidsramme: Up to day 28
Up to day 28
Number of patients with clinical significant findings in vital signs
Tidsramme: Up to day 15
Up to day 15
Investigator assessed tolerability on a 4 point scale
Tidsramme: day 42
day 42
Amount of drug excreted in urine
Tidsramme: Up to day 15
Up to day 15
Drug plasma concentration
Tidsramme: Up to day 28
Up to day 28
Monoepoxysqualene (MES) plasma concentration
Tidsramme: Up to day 28
Up to day 28

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Hjælpsomme links

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. januar 2000

Primær færdiggørelse (Faktiske)

1. maj 2000

Datoer for studieregistrering

Først indsendt

28. august 2014

Først indsendt, der opfyldte QC-kriterier

28. august 2014

Først opslået (Skøn)

1. september 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

1. september 2014

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

28. august 2014

Sidst verificeret

1. august 2014

Mere information

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 Placebo

Abonner