- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00645190
A Randomized, Double-blind, Flexible Dose, Multicenter Study to Evaluate the Effectiveness and Safety of Galantamine IR in Mild to Moderate Alzheimer's Disease
18. maj 2011 opdateret af: Xian-Janssen Pharmaceutical Ltd.
A Randomized, Double Blind, Active Control, Flexible Dose, Multicenter Study to Evaluate Galantamine HBr in the Treatment of Alzheimer's Disease:Safety and Effectiveness of an Immediate-release Table Formulation.
The purpose of this randomized, double-blind, active-controlled, flexible dosage, multicenter study is to evaluate the effectiveness and safety of galantamine tablet (16-24mg/day) for 16 weeks in the treatment of mild to moderate Alzheimer's Disease (AD) comparing with Donepezil.
Studieoversigt
Detaljeret beskrivelse
This is a randomized, double-blind, active-controlled, flexible dosage, multicenter study to evaluate the effectiveness and safety of galantamine tablet in the treatment of mild to moderate AD.
The comparator is Donepezil tablet.
At least 206 patients were to be randomized in the study.
The study consisted of 3 phases: a screening phase, a single-blind run-in phase and a double-blind treatment phase.
Screening phase is less than 2 week for eligible assessment; If the patient was taking any anti-dementia drug at screening, he/she had to stop these drugs and enter into the single-blind run-in phase.
The patient who did not take any anti-dementia drug can enter into baseline directly.
During the single-blind run-in phase, all eligible patients will take placebo twice daily for 4 weeks.
Double-blind treatment phase is 16 weeks.
At baseline, all patients who are still eligible for inclusion/exclusion criteria will be randomized to either galantamine group or donepezil group at 1:1 ratio, drugs will be taken twice daily by a flexible dose for 16 weeks.
Dose will be titrated during the first 9-12 weeks.
Dose will be fixed to 16mg/day or 24mg/day based on tolerability of the patient judged by the investigator.
The primary effectiveness endpoint is changes in ADAS-cog/11 at week 16 from baseline, secondary endpoint is responder rate in term of ADAS-cog/11.
Safety evaluation included adverse events, physical examination, ECG, and safety laboratory tests.
Study drug are taken orally twice a day.
The treatment duration was 16 weeks.
Initial galantamine dose is 8 mg/day, dose was increased to 16mg/day at week 5 and to 24 mg/day at week 9.
At week 12, dose was fixed to either 16mg/day or 24mg/day at the discretion of investigators.
Initial donepezil dose is 5mg/day, dose was then increased to 10mg/day at week 9.
At week 12, dose was fixed to either 5mg/day or 10mg/day at the discretion of investigators.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
215
Fase
- Fase 3
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
40 år og ældre (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Out-patients diagnosed with mild to moderate probable AD. The diagnosis should have been established in accordance with the classification for probable AD of NINCDS-ADRDA
- MMSE score of 10-24 (inclusive) at screening
- Patients who lived with or had regular daily visits from a responsible caregiver
- .Has signed the informed consent form by subject and assent form by care-giver
Exclusion Criteria:
- Patients with neurodegenerative disorders such as Parkinson's disease
- Patients with some conditions possibly resulting in cognitive impairment, e.g. acute cerebral trauma, infection
- Has evidence of multi-infarct dementia or clinically active cerebrovascular disease.
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
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
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Primary endpoint (ADAS-cog/11) decreased 5.4 ± 6.4 and 4 .0 ± 7.3 in galantamine and Donepezil group respectively after 16-week treatment from baseline of 22.5 ± 9.3 and 23.3 ± 9.7 respectively, showing the non-inferiority in term of efficacy.
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Sekundære resultatmål
Resultatmål |
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Secondary endpoint is responder rate. It showed 78% responder rate in galantamine group and 58% responder rate in Donepezil group after 16 weeks.
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
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.
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. marts 2004
Studieafslutning (Faktiske)
1. februar 2005
Datoer for studieregistrering
Først indsendt
24. marts 2008
Først indsendt, der opfyldte QC-kriterier
24. marts 2008
Først opslået (Skøn)
27. marts 2008
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
19. maj 2011
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
18. maj 2011
Sidst verificeret
1. marts 2010
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Psykiske lidelser
- Hjernesygdomme
- Sygdomme i centralnervesystemet
- Sygdomme i nervesystemet
- Neurokognitive lidelser
- Neurodegenerative sygdomme
- Demens
- Tauopatier
- Alzheimers sygdom
- Lægemidlers fysiologiske virkninger
- Neurotransmittermidler
- Molekylære mekanismer for farmakologisk virkning
- Autonome agenter
- Agenter fra det perifere nervesystem
- Kolinerge midler
- Enzymhæmmere
- Nootropiske midler
- Cholinesterasehæmmere
- Parasympathomimetika
- Galantamin
Andre undersøgelses-id-numre
- CR005803
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 .
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