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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT04374136




Registration number
NCT04374136
Ethics application status
Date submitted
23/04/2020
Date registered
5/05/2020
Date last updated
26/07/2024

Titles & IDs
Public title
A Phase 3 Study to Evaluate Efficacy and Safety of AL001 in Frontotemporal Dementia (INFRONT-3)
Scientific title
A Phase 3, Multicenter, Randomized, Double Blind, Placebo Controlled Study to Evaluate the Efficacy and Safety of AL001 in Individuals at Risk for or With Frontotemporal Dementia Due to Heterozygous Mutations in the Progranulin Gene
Secondary ID [1] 0 0
AL001-3
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Frontotemporal Dementia 0 0
Condition category
Condition code
Neurological 0 0 0 0
Dementias
Neurological 0 0 0 0
Alzheimer's disease
Mental Health 0 0 0 0
Other mental health disorders
Neurological 0 0 0 0
Other neurological disorders
Neurological 0 0 0 0
Neurodegenerative diseases

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - AL001
Treatment: Drugs - Placebo
Treatment: Drugs - Open label - AL001

Experimental: AL001 - AL001 every 4 weeks

Placebo comparator: Placebo - Placebo every 4 weeks

Experimental: Open label - AL001 - AL001 every 4 weeks


Treatment: Drugs: AL001
Administered via intravenous (IV) infusion

Treatment: Drugs: Placebo
Administered via intravenous (IV) infusion

Treatment: Drugs: Open label - AL001
Administered via intravenous (IV) infusion
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Evaluation of efficacy of AL001 as measured by the CDR® plus NACC FTLD-SB
Timepoint [1] 0 0
Through study completion, on average up to 96 weeks
Secondary outcome [1] 0 0
Change in Clinical Global Impression-Severity (CGI-S) Score
Timepoint [1] 0 0
Baseline to 96 weeks
Secondary outcome [2] 0 0
Change in Clinical Global Impression-Improvement (CGI-I) Score
Timepoint [2] 0 0
Baseline to 96 weeks
Secondary outcome [3] 0 0
Change in Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) Score
Timepoint [3] 0 0
Baseline to 96 weeks
Secondary outcome [4] 0 0
Pharmacodynamic Biomarkers
Timepoint [4] 0 0
Baseline to 96 weeks
Secondary outcome [5] 0 0
Evaluation of safety and tolerability of AL001: Incidence of adverse events
Timepoint [5] 0 0
Baseline to 96 weeks

Eligibility
Key inclusion criteria
* Persons with a progranulin gene mutation and at risk of developing FTD symptoms as evidenced by a biomarker, or persons with a progranulin gene mutation and diagnosed with FTD.
* If symptomatic, one or more of the criteria for the diagnosis of possible behavioral variant FTD, or a diagnosis of Primary Progressive Aphasia.
* Study partner who consents to study participation and who cares for/visits the participant daily for at least 5 hours per week.
* Written informed consent must be obtained and documented (from the participant or, where jurisdictions allow it, from their legal decision maker).
Minimum age
25 Years
Maximum age
85 Years
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
* Dementia due to a condition other than FTD including, but not limited to, Alzheimer's disease, Parkinson's disease, dementia with Lewy bodies, Huntington disease, or vascular dementia.
* Known history of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric, human, or humanized antibodies or fusion proteins.
* Current uncontrolled hypertension, diabetes mellitus or thyroid disease. Clinically significant heart disease, liver disease or kidney disease. History or evidence of clinically significant brain disease other than FTD.
* Females who are pregnant or breastfeeding, or planning to conceive within the study period.
* Any experimental vaccine or gene therapy.
* History of cancer within the last 5 years.
* Current use of anticoagulant medications (e.g., coumadin, heparinoids, apixaban).
* Residence in a skilled nursing facility, convalescent home, or long term care facility at screening; or requires continuous nursing care.

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 administering the treatment/s
The people assessing the outcomes
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
Active, not recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
23/07/2020
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
11/10/2027
Actual
Sample size
Target
110
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
Box Hill Hospital - Box Hill
Recruitment hospital [2] 0 0
Royal Prince Alfred Hospital - Camperdown
Recruitment hospital [3] 0 0
The Queen Elizabeth Hospital - Woodville
Recruitment postcode(s) [1] 0 0
3128 - Box Hill
Recruitment postcode(s) [2] 0 0
2050 - Camperdown
Recruitment postcode(s) [3] 0 0
- Woodville
Recruitment outside Australia
Country [1] 0 0
United States of America
State/province [1] 0 0
Arizona
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United States of America
State/province [2] 0 0
California
Country [3] 0 0
United States of America
State/province [3] 0 0
Colorado
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United States of America
State/province [4] 0 0
Florida
Country [5] 0 0
United States of America
State/province [5] 0 0
Georgia
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United States of America
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Indiana
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United States of America
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Kansas
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United States of America
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Maryland
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Minnesota
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New York
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North Carolina
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Ohio
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Oregon
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Pennsylvania
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Tennessee
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United States of America
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Texas
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United States of America
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Wisconsin
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Argentina
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Ciudad Autónoma De BuenosAires
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Argentina
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Buenos Aires
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Argentina
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San Juan
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Belgium
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Vlaams Brabant
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Canada
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London
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Canada
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Toronto
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France
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Haute-Garonne
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France
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Seinne-Maritime
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France
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Bordeaux
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France
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Lille
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France
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Paris
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Germany
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Köln
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Germany
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Ulm
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Greece
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Attica
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Greece
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Evros
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Italy
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Emilia Romagna
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Italy
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Palermo
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Italy
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Baggiovara
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Italy
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Bologna
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Italy
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Brescia
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Italy
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Milano
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Italy
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Tricase
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Netherlands
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Rotterdam
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Portugal
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Coimbra
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Portugal
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Lisboa
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Portugal
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Porto
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Spain
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Cantabria
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Spain
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Barcelona
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Spain
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Donostia-san Sebastián
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Spain
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Madrid
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Sweden
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Huddinge
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Switzerland
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Basel
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Turkey
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Balcova
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Turkey
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Fatih
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United Kingdom
State/province [52] 0 0
London

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Alector Inc.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
TBD TBD
Address 0 0
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

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.

Results not provided in https://clinicaltrials.gov/study/NCT04374136