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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/show/NCT02670083




Registration number
NCT02670083
Ethics application status
Date submitted
28/01/2016
Date registered
1/02/2016
Date last updated
24/09/2019

Titles & IDs
Public title
CREAD Study: A Study of Crenezumab Versus Placebo to Evaluate the Efficacy and Safety in Participants With Prodromal to Mild Alzheimer's Disease (AD)
Scientific title
A Phase III, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Efficacy And Safety Study of Crenezumab in Patients With Prodromal to Mild Alzheimer's Disease
Secondary ID [1] 0 0
BN29552
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Alzheimer's Disease 0 0
Condition category
Condition code
Neurological 0 0 0 0
Alzheimer's disease
Neurological 0 0 0 0
Dementias

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Crenezumab
Treatment: Drugs - Placebo

Experimental: Crenezumab - Participants will receive IV infusion of crenezumab q4w for 100 weeks.

Placebo Comparator: Placebo - Participants will receive placebo q4w for 100 weeks.


Treatment: Drugs: Crenezumab
Crenezumab will be administered by IV infusion q4w for 100 weeks.

Treatment: Drugs: Placebo
Placebo will be administered as IV infusion q4w for 100 weeks.

Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Change from baseline to Week 105 in Clinical Dementia Rating-Sum of Boxes (CDR-SB) Score
Timepoint [1] 0 0
Baseline, Week 105
Secondary outcome [1] 0 0
Change from Baseline to Week 105 on Cognition, as assessed by Alzheimer's Disease Assessment Scale-Cognition (ADAS-Cog) (subscales) 13 (ADAS-Cog-13) and 11 (ADAS-Cog-11)
Timepoint [1] 0 0
Baseline, Week 105
Secondary outcome [2] 0 0
Change from Baseline to Week 105 on Severity of Dementia, Assessed Using the CDR-Gloal Score (CDR-GS)
Timepoint [2] 0 0
Baseline, Week 105
Secondary outcome [3] 0 0
Change from Baseline to Week 105 on Severity of Dementia, Assessed Using the Mini Mental State Evaluation (MMSE)
Timepoint [3] 0 0
Baseline, Week 105
Secondary outcome [4] 0 0
Change from Baseline to Week 105 on function as assessed by the ADCS-ADL total score and the ADCS-instrumental subscore
Timepoint [4] 0 0
Baseline, Week 105
Secondary outcome [5] 0 0
Change from Baseline to Week 105 on a measure of dependence derived from the ADCS-ADL score
Timepoint [5] 0 0
Baseline, Week 105
Secondary outcome [6] 0 0
Change from Baseline to Week 105 assessed using the Neuropsychiatric Inventory Questionnaire (NPI-Q)
Timepoint [6] 0 0
Baseline, Week 105
Secondary outcome [7] 0 0
Quality of Life-Alzheimer's Disease (QoL-AD) Scale Score
Timepoint [7] 0 0
Baseline up to Week 105
Secondary outcome [8] 0 0
Zarit Caregiver Interview for Alzheimer's Disease (ZCI-AD) Scale Score
Timepoint [8] 0 0
Baseline up to Week 105
Secondary outcome [9] 0 0
EQ-5D Questionnaire Domain Score
Timepoint [9] 0 0
Baseline up to Week 105
Secondary outcome [10] 0 0
Percentage of Participants with Adverse Event (AEs) and Serious Adverse Event (SAEs)
Timepoint [10] 0 0
Up to Week 105
Secondary outcome [11] 0 0
Percentage of Participants with Anti-Crenezumab Antibodies
Timepoint [11] 0 0
Baseline up to Week 105
Secondary outcome [12] 0 0
Serum Concentration of Crenezumab
Timepoint [12] 0 0
Pre-infusion (0 hour), 60-90 minutes post-infusion on Day 1 Week 1 and on Week 25; Weeks 5, 13, 37, 53, and 100 (infusion length = as per the Pharmacy Manual)
Secondary outcome [13] 0 0
Plasma Amyloid Beta (Abeta) Concentrations
Timepoint [13] 0 0
Screening (Weeks -8 to -1) ; Day 1 Week 1; Weeks 5, 25, 53, and 100
Secondary outcome [14] 0 0
Change from Baseline to Week 105 in Brain Volume as Determined by Magnetic Resonance Imaging (MRI)
Timepoint [14] 0 0
Baseline, Week 105
Secondary outcome [15] 0 0
Cerebrospinal Fluid (CSF) Concentration of Crenezumab
Timepoint [15] 0 0
At pre-defined intervals from baseline through week 105
Secondary outcome [16] 0 0
Brain Amyloid Load Over Time Measured by Amyloid-PET
Timepoint [16] 0 0
At pre-defined intervals from baseline through week 105
Secondary outcome [17] 0 0
Brain Tau Load Over Time Measured by Tau-PET
Timepoint [17] 0 0
At pre-defined intervals from baseline through week 105
Secondary outcome [18] 0 0
Cerebrospinal Fluid (CSF) Markers of Disease Over Time
Timepoint [18] 0 0
At pre-defined intervals from baseline through week 105

Eligibility
Key inclusion criteria
- Weight between 40 and 120 kilograms (Kg) inclusive

- Availability of a person (referred to as the "caregiver") who in the investigator's
judgment:

- Has frequent and sufficient contact with the participant to be able to provide
accurate information regarding the participant's cognitive and functional abilities,
agrees to provide information at clinic visits (which require partner input for scale
completion), signs the necessary consent form, and has sufficient cognitive capacity
to accurately report upon the participant's behavior and cognitive and functional
abilities

- Fluency in the language of the tests used at the study site

- Adequate visual and auditory acuity, in the investigator's judgment, sufficient to
perform the neuropsychological testing (eye glasses and hearing aids are permitted)

- Evidence of the AD pathological process, by a positive amyloid assessment either on
cerebrospinal fluid (CSF) amyloid beta 1-42 levels as measured on the Elecsys
beta-amyloid(1-42) test system or amyloid PET scan by qualitative read by the
core/central PET laboratory

- Demonstrated abnormal memory function at screening

- Screening mini mental state examination (MMSE) score of greater than or equal to (>=)
22 points and Clinical Dementia Rating-Global Score (CDR-GS) of 0.5 or 1.0

- Meets National Institute on Aging/Alzheimer's Association (NIAAA) core clinical
criteria for probable AD dementia or prodromal AD (consistent with the NIAAA
diagnostic criteria and guidelines for mild cognitive impairment (MCI)

- If receiving symptomatic AD medications, the dosing regimen must have been stable for
3 months prior to screening
Minimum age
50 Years
Maximum age
85 Years
Gender
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
- Any evidence of a condition other than AD that may affect cognition such as other
dementias, stroke, brain damage, autoimmune disorders (e.g. multiple sclerosis) or
infections with neurological sequelae.

- History of major psychiatric illness such as schizophrenia or major depression (if not
considered in remission)

- At risk of suicide in the opinion of the investigator

- Presence of significant cerebral vascular pathology as assessed by MRI central reader

- Unstable or clinically significant cardiovascular, kidney or liver disease (e.g.,
myocardial infarction)

- Uncontrolled hypertension

- Screening hemoglobin A1c (HbA1C) >8%

- Poor peripheral venous access

- History of cancer except:

If considered to be cured or If not being actively treated with anti-cancer therapy or
radiotherapy

- Known history of severe allergic, anaphylactic, or other hypersensitivity reactions to
chimeric, human, or humanized antibodies or fusion proteins

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s


The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint(s)
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
SA,VIC,WA
Recruitment hospital [1] 0 0
The Queen Elizabeth Hospital; Neurology - Woodville
Recruitment hospital [2] 0 0
Caulfield Hospital; Aged Psychiatry Research Unit - Caulfield
Recruitment hospital [3] 0 0
Heidelberg Repatriation Hospital; Medical and Cognitive Research Centre - Heidelberg West
Recruitment hospital [4] 0 0
Neurodegenerative Disorders Research; Neurology - West Perth
Recruitment postcode(s) [1] 0 0
5011 - Woodville
Recruitment postcode(s) [2] 0 0
3162 - Caulfield
Recruitment postcode(s) [3] 0 0
3081 - Heidelberg West
Recruitment postcode(s) [4] 0 0
6005 - West Perth
Recruitment outside Australia
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Burgos
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Mölndal
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Basel
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Istanbul
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Samsun
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Ukraine
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KIEV Governorate
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Ukraine
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Kiev
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United Kingdom
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Chertsey
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Coventry
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Newcastle Upon Tyne
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Oxford
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Preston
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United Kingdom
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Torquay

Funding & Sponsors
Primary sponsor type
Commercial sector/Industry
Name
Hoffmann-La Roche
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
This randomized, double-blind, placebo-controlled, parallel group study will evaluate the
efficacy and safety of crenezumab versus placebo in participants with prodromal to mild AD.
Participants will be randomized 1:1 to receive either intravenous (IV) infusion of crenezumab
or placebo every 4 weeks (q4w) for 100 weeks. The final efficacy and safety assessment will
be performed 52 weeks after the last crenezumab dose.
Trial website
https://clinicaltrials.gov/show/NCT02670083
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Clinical Trials
Address 0 0
Hoffmann-La Roche
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Summary results
Other publications