A Study of Semagacestat for Alzheimer's Patients (Identity XT)
22 september 2014 bijgewerkt door: Eli Lilly and Company
Open-Label Extension for Alzheimer's Disease Patients Who Complete One of Two Semagacestat Phase 3 Double-Blind Studies (H6L-MC-LFAN or H6L-MC-LFBC)
The primary objective of the original study was to assess the safety of semagacestat in Alzheimer's disease (AD) patients during 24 months of open-label treatment. Baseline for the efficacy measures is defined as the baseline for feeder studies LFAN (NCT00594568) and LFBC (NCT00762411). For all safety analyses (adverse events), baseline for patients will be week 0 of this study (LFBF).
Preliminary results from LFAN and LFBC showed semagacestat did not slow disease progression and was associated with worsening of clinical measures of cognition and the ability to perform activities of daily living. Study drug was stopped in all studies. Studies LFAN, LFBC and LFBF have been amended to continue collecting safety data, including cognitive scores, for at least seven months. The CT-Registry will reflect results of analyses from the original protocol in addition to those from the amended protocol. Very few participants from LFBC rolled over into LFBF (N = 9). Due to insufficient sample size, the data for LFBC participants who rolled into LFBF were not analyzed.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Studietype
Ingrijpend
Inschrijving (Werkelijk)
180
Fase
- Fase 3
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
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New South Wales
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Kogarah, New South Wales, Australië, 2217
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Victoria
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Geelong, Victoria, Australië, 3220
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Heidelberg West, Victoria, Australië, 3081
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British Columbia
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Kelowna, British Columbia, Canada, V1Y3G8
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Penticton, British Columbia, Canada, V2A5C8
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Quebec
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Sherbrooke, Quebec, Canada, J1H1Z1
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Antofagasta, Chili
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Santiago, Chili
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Valdivia, Chili
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Hannover, Duitsland, 30559
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Muenchen, Duitsland, 81675
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Regensburg, Duitsland, D-93053
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Siegen, Duitsland, 57072
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Kuopio, Finland, 70210
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Oulu, Finland, 90229
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Toulouse, Frankrijk, TSA 60033
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Ashkelon, Israël, 78306
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Petah Tikva, Israël, 49100
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Tel Hashomer, Israël, 52661
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Milano, Italië, 20132
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Fukui, Japan, 910-3113
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Fukuoka, Japan, 770-8076
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Kochi, Japan, 780-0842
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Tokushima, Japan, 770-0852
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Lublin, Polen, 20-950
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Poznan, Polen, 61- 485
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Barcelona, Spanje, 08003
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Plasencia, Spanje, 10600
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Arizona
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Phoenix, Arizona, Verenigde Staten, 85004
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Sun City, Arizona, Verenigde Staten, 85351
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Tucson, Arizona, Verenigde Staten, 85741
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California
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Costa Mesa, California, Verenigde Staten, 92626
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Fresno, California, Verenigde Staten, 93720
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Laguna Hills, California, Verenigde Staten, 92653
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Lomita, California, Verenigde Staten, 90717
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Orange, California, Verenigde Staten, 92868
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San Diego, California, Verenigde Staten, 92103
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San Francisco, California, Verenigde Staten, 94109
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Santa Monica, California, Verenigde Staten, 90404
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Connecticut
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Hamden, Connecticut, Verenigde Staten, 06518
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New Haven, Connecticut, Verenigde Staten, 06510
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District of Columbia
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Washington, District of Columbia, Verenigde Staten, 20057
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Florida
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Brooksville, Florida, Verenigde Staten, 34601
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Deerfield Beach, Florida, Verenigde Staten, 33064
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Fort Lauderdale, Florida, Verenigde Staten, 33308
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Fort Myers, Florida, Verenigde Staten, 33912
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Hollywood, Florida, Verenigde Staten, 33021
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Miami, Florida, Verenigde Staten, 33137
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Orlando, Florida, Verenigde Staten, 32806
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St Petersburg, Florida, Verenigde Staten, 33716
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Tampa Bay, Florida, Verenigde Staten, 33613
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Indiana
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Indianapolis, Indiana, Verenigde Staten, 46202
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Kentucky
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Lexington, Kentucky, Verenigde Staten, 40503
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Louisiana
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New Orleans, Louisiana, Verenigde Staten, 70131
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Shreveport, Louisiana, Verenigde Staten, 71104
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Massachusetts
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Hyannis, Massachusetts, Verenigde Staten, 02601
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Missouri
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St Louis, Missouri, Verenigde Staten, 63108
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New York
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New York, New York, Verenigde Staten, 10032
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North Carolina
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Durham, North Carolina, Verenigde Staten, 27705
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Raleigh, North Carolina, Verenigde Staten, 27607
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Winston-Salem, North Carolina, Verenigde Staten, 27103
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Ohio
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Toledo, Ohio, Verenigde Staten, 43623
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Oklahoma
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Oklahoma City, Oklahoma, Verenigde Staten, 73116
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Oregon
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Eugene, Oregon, Verenigde Staten, 97401
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Pennsylvania
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Jenkintown, Pennsylvania, Verenigde Staten, 19046
- For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician.
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Philadelphia, Pennsylvania, Verenigde Staten, 19104
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Rhode Island
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East Providence, Rhode Island, Verenigde Staten, 02914
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South Carolina
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North Charleston, South Carolina, Verenigde Staten, 29406
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Vermont
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Bennington, Vermont, Verenigde Staten, 05201
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Bellville, Zuid-Afrika, 7530
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Stockholm, Zweden, 14186
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Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
55 jaar en ouder (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Beschrijving
Inclusion Criteria:
- Meets National Institute of Neurological and Communicative Disorders and Stroke/Alzheimer's Disease and Related Disorders Association (NINCDS/ADRDA) criteria for probable Alzheimer's Disease
- Completed semagacestat study LFAN or study LFBC through 88 weeks
- Must continue to have a reliable caregiver
- Capable of swallowing whole oral medication
- Agrees not to participate in other investigational compounds for the duration of study
Exclusion Criteria:
- Meets LFAN or LFBC study discontinuation criteria at the last visit of the LFAN or LFBC study
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Drug: semagacestat
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140mg administered orally, once daily for 24 months; dose reduction to 100mg or 60 mg possible due to intolerability
Andere namen:
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Change From Baseline in Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog11) at Week 16 After Cessation of Study Drug
Tijdsspanne: Baseline (LFAN randomization), 16 weeks (LFBF) after cessation of study drug
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The cognitive subscale of the ADAS (ADAS-Cog11) consists of 11 items assessing areas of function most typically impaired in Alzheimer's Disease (AD): orientation, verbal memory, language, and praxis.
The scale ranges from 0 to 70, with higher scores indicating greater disease severity.
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Baseline (LFAN randomization), 16 weeks (LFBF) after cessation of study drug
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Change From Baseline in Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory (ADCS-ADL) at Week 16 After Cessation of Study Drug
Tijdsspanne: Baseline (LFAN randomization), 16 weeks (LFBF) after cessation of study drug
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The ADCS-ADL is a 23-item inventory developed as a rater-administered questionnaire answered by the participant's caregiver.
It measures both basic and instrumental activities of daily living.
The total score ranges from 0 to 78, with lower scores indicating greater disease severity.
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Baseline (LFAN randomization), 16 weeks (LFBF) after cessation of study drug
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Percent Change From Baseline in Amyloid Beta (Aβ) 1-42 Plasma Concentration at Week 12
Tijdsspanne: Baseline (LFAN Randomization ), 6 hours pose-dose at Week 12 (LFBF)
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Concentration of amino acid peptide known as Aβ 1-42 in plasma.
Least Square (LS) Mean value was controlled for baseline value, age, and investigator.
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Baseline (LFAN Randomization ), 6 hours pose-dose at Week 12 (LFBF)
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Change From Baseline in Hippocampal Volume Using Volumetric Magnetic Resonance Imaging (vMRI) at Week 12
Tijdsspanne: Baseline (LFAN Randomization), 12 weeks (LFBF)
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The vMRI assessment of right hippocampal and left hippocampal volume is reported.
Least Square (LS) Mean value was controlled for baseline value, age, and investigator.
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Baseline (LFAN Randomization), 12 weeks (LFBF)
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Change From Baseline in Amyloid Imaging Positron Emission Tomography (AV-45-PET) at Week 12
Tijdsspanne: Baseline (LFAN Randomization), 12 weeks (LFBF)
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A radioactive tracer for PET that is a ligand for amyloid called [18F]-AV-45.
This permits the visualization of amyloid in the brains of Alzheimer's participants.
The outcome reported is the composite summary of the standard uptake value ratio for the cerebellar gray matter.
Least Squares (LS) Mean value was controlled for baseline value, age, and investigator.
Due to insufficient sample size, this analysis was not done.
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Baseline (LFAN Randomization), 12 weeks (LFBF)
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Change From Baseline in Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog11) at Week 12
Tijdsspanne: Baseline (LFAN Randomization), 12 weeks (LFBF)
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The cognitive subscale of the ADAS (ADAS-Cog11) consists of 11 items assessing areas of function most typically impaired in Alzheimer's Disease (AD): orientation, verbal memory, language, and praxis.
The scale ranges from 0 to 70, with higher scores indicating greater disease severity.
Least Square (LS) Mean value was controlled for baseline value, age, investigator, and concomitant standard of care (SOC) medication.
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Baseline (LFAN Randomization), 12 weeks (LFBF)
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Change From Baseline in Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog12) at Week 12
Tijdsspanne: Baseline (LFAN Randomization), 12 weeks (LFBF)
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ADAS-Cog12 is the ADAS-Cog11 augmented with the delayed free recall measure, resulting in a total score ranging from 0 to 80. Higher scores indicate greater disease severity.
Least Square (LS) Mean value was controlled for baseline value, age, investigator, and concomitant standard of care (SOC) medication.
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Baseline (LFAN Randomization), 12 weeks (LFBF)
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Change From Baseline in Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog14) at Week 12
Tijdsspanne: Baseline (LFAN Randomization), 12 weeks (LFBF)
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The ADAS-Cog14 is the ADAS-Cog11 augmented with delayed free recall, digit cancellation, and maze completion measures.
A score of 0 to 10 for delayed free recall and a conversion code of 0 to 5 for digit cancellation and maze completion provide total score ranges for this extended ADAS-Cog14 of 0 to 90.
Higher scores indicate greater disease severity.
Least Square (LS) Mean value was controlled for the baseline value, age, investigator, and concomitant standard of care (SOC) medication.
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Baseline (LFAN Randomization), 12 weeks (LFBF)
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Change From Baseline in Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory (ADCS-ADL) at Week 12
Tijdsspanne: Baseline (LFAN Randomization), 12 weeks (LFBF)
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The ADCS-ADL is a 23-item inventory developed as a rater-administered questionnaire answered by the participant's caregiver.
It measures both basic and instrumental activities of daily living.
The total score ranges from 0 to 78, with lower scores indicating greater disease severity.
Least Square (LS) Mean value was controlled for baseline value, age, investigator, and concomitant standard of care (SOC) medication.
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Baseline (LFAN Randomization), 12 weeks (LFBF)
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Mean Concentration of LY450139
Tijdsspanne: 3 months (pre-dose, 2, 4, and 6 hours after dosing )(LFBF)
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3 months (pre-dose, 2, 4, and 6 hours after dosing )(LFBF)
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Change From Baseline in Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog12) at Week 16 After Cessation of Study Drug
Tijdsspanne: Baseline (LFAN Randomization), 16 weeks (LFBF) after cessation of study drug
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ADAS-Cog12 is the ADAS-Cog11 augmented with the delayed free recall measure, resulting in a total score ranging from 0 to 80. Higher scores indicate greater disease severity.
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Baseline (LFAN Randomization), 16 weeks (LFBF) after cessation of study drug
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Change From Baseline in Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog14) at Week 16 After Cessation of Study Drug
Tijdsspanne: Baseline (LFAN Randomization), 16 weeks (LFBF) after cessation of study drug
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The ADAS-Cog14 is the ADAS-Cog11 augmented with delayed free recall, digit cancellation, and maze completion measures.
A score of 0 to 10 for delayed free recall and a conversion code of 0 to 5 for digit cancellation and maze completion provide total score ranges for this extended ADAS-Cog14 of 0 to 90.
Higher scores indicate greater disease severity.
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Baseline (LFAN Randomization), 16 weeks (LFBF) after cessation of study drug
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Change From Baseline in Clinical Dementia Rating Scale (Sum of Boxes) (CDR-SB) at Week 24
Tijdsspanne: Baseline (LFAN Randomization), 24 weeks (LFBF)
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The CDR-SB is a semi-structured interview of participants and their caregivers.
The participant's cognitive status is rated in 6 domains of functioning, including memory, orientation, judgment and problem solving, community affairs, home and hobbies, and personal care.
A severity score is assigned for each of the 6 domains with total score ranging from 0 to 18. Higher scores indicate greater disease severity.
Least Square (LS) Mean value was controlled for baseline value, age, investigator, and concomitant standard of care (SOC) medication.
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Baseline (LFAN Randomization), 24 weeks (LFBF)
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Change From Baseline in Mini-Mental State Examination (MMSE) at Week 24
Tijdsspanne: Baseline (LFAN Randomization), 24 weeks (LFBF)
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The MMSE is a brief screening instrument used to assess cognitive function in elderly participants.
It assesses orientation, memory, attention, and ability to name objects, follow verbal and written commands, write a sentence, and copy figures.
The total score ranges from 0 to 30, with a lower score indicating greater disease severity.
Least Square (LS) Mean value was controlled for baseline value, age, investigator, and concomitant standard of care (SOC) medication.
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Baseline (LFAN Randomization), 24 weeks (LFBF)
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Change From Baseline in Neuropsychiatric Inventory (NPI) at Week 24
Tijdsspanne: Baseline (LFAN Randomization), 24 weeks (LFBF)
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The NPI is a tool for assessing psychopathology in patients with dementia and other neurologic disorders.
Information is obtained from a caregiver familiar with the patient's behavior.
The score ranges from 12 to 144, with higher scores indicating greater disease severity.
Least Square (LS) Mean value was controlled for the baseline value, age, investigator, concomitant standard of care medication.
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Baseline (LFAN Randomization), 24 weeks (LFBF)
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Change From Baseline in EuroQol-5D (EQ-5D) at Week 24
Tijdsspanne: Baseline (LFAN Randomization), 24 weeks (LFBF)
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EQ-5D (proxy version) measures mobility, self-care, usual activities, pain/discomfort, anxiety/depression; each has 3 severity levels (no, some, severe problems) coded to a 1-digit number (1-3).
Digits are combined into 5-digit number describing health state.
Numbers 1-3 are not added for total score.
Visual Analog Scale (VAS) assesses caregiver's impression of participant's overall health state; VAS scores range=0-100, with lower scores indicating greater disease severity.
LS Mean value was controlled for baseline value, age, investigator, and concomitant standard of care (SOC) medication.
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Baseline (LFAN Randomization), 24 weeks (LFBF)
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Change From Baseline in Resource Utilization in Dementia-Lite Questionnaire (RUD-Lite) at Week 12
Tijdsspanne: Baseline (LFAN Randomization), 12 weeks (LFBF)
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RUD-Lite assesses the healthcare resource utilization of participants and their caregivers to determine the level of formal and informal care attributable to Alzheimer's Disease (AD).
Information on both caregivers (caregiving time, work status) and participants (accommodation and healthcare resource utilization) is collected from the baseline and follow-up interviews.
Reported the change in number of hospitalizations per participant to week 12.
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Baseline (LFAN Randomization), 12 weeks (LFBF)
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Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 december 2009
Primaire voltooiing (Werkelijk)
1 april 2011
Studie voltooiing (Werkelijk)
1 april 2011
Studieregistratiedata
Eerst ingediend
17 december 2009
Eerst ingediend dat voldeed aan de QC-criteria
17 december 2009
Eerst geplaatst (Schatting)
18 december 2009
Updates van studierecords
Laatste update geplaatst (Schatting)
25 september 2014
Laatste update ingediend die voldeed aan QC-criteria
22 september 2014
Laatst geverifieerd
1 september 2014
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 5930
- H6L-MC-LFBF (Andere identificatie: Eli Lilly and Company)
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