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Recruiting NCT06372821

A Trial Evaluating the Effect of NIO752 on Tau Synthesis Measured by a Process Known as SILK

Phase I Interventional Alzheimer Disease Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 2 (Disorder) Autosomal Dominant Alzheimer Disease Due to Mutation of Amyloid Precursor Protein (Disorder)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: NIO752, Placebo.
Who it may be relevant to
Registry conditions: Alzheimer Disease, Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder), Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 2 (Disorder), Autosomal Dominant Alzheimer Disease Due to Mutation of Amyloid Precursor Protein (Disorder). Basic parameters: 21 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States, United Kingdom
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

A Randomized, Participant & Investigator Blinded, Placebo-Controlled Study to Evaluate the Ability of Intrathecally Administered NIO752 to Lower CSF Total Tau Synthesis in Participants With AD Measured by Stable Isotope Labelling Kinetics

Overview

This study will assess if drug (NIO752) reduces production of a protein, tau, by the brain. Normally tau maintains the internal skeleton of nerve cells. In Alzheimer's disease (AD) it builds up in the brain, causing damage. Abnormal tau proteins cling to each other forming 'tangles' inside nerve cells, which interfere with how the nerve cells work, and eventually die. This is what causes the symptoms of dementia. It is thought that NIO752 reduces production of tau.

Interventions

  • Drug NIO752
    Antisense oligonucleotide
  • Other Placebo
    Saline

Primary outcome measures

  • Tau synthesis rate inhibition in individuals with sporadic AD and ADAD [Time frame: Day 23]
Secondary outcome measures (5)
  • Compare efficacy of knockdown of tau production in sporadic AD and ADAD by measuring the synthesis rate of tau by determining the ratio of labelled to unlabeled tau (tracer to tracee ratio) in serial cerebrospinal fluid samples. [Time frame: Day 23]
  • Number of participants with adverse events [safety and tolerability] [Time frame: Day 0 to Day 145]
  • Comparison of number of Adverse Events reported between participants receiving one dose of NIO752 versus those receiving two doses of NIO752. [Time frame: Day 0 to Day 145]
  • Compare rates of tau synthesis and clearance in sporadic AD and ADAD [Time frame: Day 23]
  • Determine CSF tau concentration to tau production relationships in humans [Time frame: 120 days]

Eligibility criteria

Inclusion criteria

  • Able to provide signed informed consent.
  • Between 21 to 80 years old (inclusive).
  • A diagnosis of mild or moderate Alzheimer's disease by a Clinical Dementia Rating score of 0.5 to 2, where the investigator believes they will be able to complete the study.
  • A history of cerebrospinal fluid, Positron Emission Topography (PET), or blood-based biomarkers supporting the diagnosis of Alzheimer's disease, or symptomatic approved presenilin (PSEN) or amyloid precursor protein (APP) mutation carriers. If blood biomarkers are equivocal then amyloid status can be confirmed using cerebrospinal fluid.
  • Fluency in English
  • Participant has a reliable study partner or caregiver
  • Able to undergo lumbar punctures, magnetic resonance imaging (MRI), cerebrospinal fluid draws, and blood draws.
  • Individuals will be willing to consent for their biological samples and personal data to be shared with the commercial partner (Novartis)

Exclusion criteria

  • Live in a skilled nursing facility or dementia care facility.
  • Any clinically significant laboratory abnormality
  • Attempted suicide, suicidal ideation with a plan that required hospital admission within 12 months prior to Screening
  • Any previous use of experimental therapy within 180 days or 5 half-lives prior to Day 1, whichever is greater.
  • Any previous use of MAPT antisense oligonucleotides (ASO) or any other ASO or other gene therapy meant as treatment for Alzheimer's disease.
  • History of hypersensitivity to any of the study treatments or its excipients or to drugs of similar chemical classes.
  • Any condition that increases risk of meningitis unless participant is receiving appropriate prophylactic treatment.
  • Current medical or non-Alzheimer's disease neurological condition that might impact cognition or performance on cognitive assessments
  • Have any other conditions which, in the opinion of the investigator, would make the participant unsuitable for inclusion or could interfere with the patient participating in or completing the study.
  • Unlikely to cooperate in the study; not able to attend scheduled examinations and visits; or not able to follow study instructions per the judgement of the investigator.
  • Current alcohol (>14 units per week) or current cannabis use; or history of alcohol or drug abuse or dependence (except nicotine dependence) within 2-years before the screening visit.
  • Treatment with immunosuppressants, antipsychotics, lithium, neuroleptics, dopaminergic agonists, L-dopa, or monoamine oxidase inhibitors at the time of screening. Current use of medications, other than cholinesterase inhibitors and/or memantine, that could alter cognition, as determined by the Investigator. If patients are taking cholinesterase inhibitors and/or memantine at screening, the dose must have been stable within 12-weeks prior to screening and must remain stable during the duration of the study.
  • Unable to undergo MRI due to for example claustrophobia, or presents absolute contraindications to MRI (e.g., metallic implants, metallic foreign bodies, pacemaker, defibrillator).
  • Significant signs of major cerebrovascular disease
  • Sexually active males, unless they agree to use a condom during intercourse from the time of consent until a minimum of 15 weeks after treatment.
  • Breast feeding women, pregnant women, and females of reproductive potential unless they use highly effective contraception methods, as specified in the protocol.
  • Patients on regular anticoagulants or anti-platelets that would preclude lumbar puncture are not eligible to participate
  • Seropositive for human immunodeficiency virus (HIV), Hepatitis B or hepatitis C.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Triple blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Washington University in St. Louis — St Louis
United Kingdom · 1 center
  • University College London Hospitals NHS Foundation Trust — London

Identifiers

NCT: NCT06372821 · 158160

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗