Alzheimer DiseasePhase 1NCT05469360
Study of Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of NIO752 in Early Alzheimer's Disease Participants
A Phase 1 study testing NIO752 in people with Alzheimer Disease and Mild Cognitive Impairment, run by Novartis Pharmaceuticals at 10 sites in 4 countries.
Trial summary
Phase 1b study to assess the pharmacodynamics, safety, tolerability, and pharmacokinetics of NIO752 in patients with early Alzheimer's disease (AD) Read more about this study
- Who is it for?
- Ages 30 to 74 years
- Conditions the study is for
- Alzheimer Disease, Mild Cognitive Impairment
- What is being tested?
- NIO752
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 38 participants
- Where
- 10 sitesin 4 countries
- Study dates
- 23 Feb 2023to 24 Sep 2027
- Phase
- Phase 1
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 30 to 74 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Main Inclusion Criteria (placebo-controlled part):
- Between 30 to 74 years old (both inclusive) at the time of informed consent.
- A diagnosis of mild Alzheimer's Disease (AD) or mild cognitive impairment (MCI) due to AD at screening with at least a 6-month decline in cognitive function prior to screening documented in the medical record. Both participants with sporadic AD as well as Amyloid Precursor Protein (APP), Presenilin-1 (PSEN1) or Presenilin-2 (PSEN2) mutation carriers are eligible.
- Participants must have a diagnosis of MCI due to AD or mild AD at screening as defined by a Clinical Dementia Rating Scale (CDR) Global Score of 0.5 or 1 and a Memory Score ≥ 0.5.
- A history of CSF biomarkers supporting the diagnosis of AD obtained at any time point prior to screening, including CSF amyloid (amyloid-β 42 and/or 42/40 ratio) AND tau species (total tau and/or phosphorylated tau). All participants must have documented historical confirmation of both CSF biomarkers (amyloid-β and tau species) with results supporting a diagnosis of AD prior to screening. This criterion will be determined individually for each participant taking into consideration the biomarker assay used in each case. For participants (Cohorts 1 \& 2 only) with no historical CSF biomarker information, a LP for CSF collection must be performed at the screening visit. For CSF collected at screening, participants must have confirmed positivity of amyloid-β-42 ≤ 1000 pg/mL as well as positivity on, at least, one of the following Tau biomarkers: phosphorylated-tau-181 > 12 pg/ml OR T-tau > 149.9 pg/mL as determined by the central laboratory.
- Participant has a reliable study partner or caregiver (e.g., spouse, sibling, close friend, adult child) who, is at least 18 years old.
- Participant resides in a proximity to the study site to allow a timely unscheduled visit to the study site, if necessary.
- Participant is able to undergo lumbar puncture (LP), CSF collections, and blood draws, tolerate brain MRI and PET scanning, and able to participate and tolerate all study procedures at study visit.
Main Inclusion Criteria (OLE part):
- Signed informed consent of protocol version inclusive of the OLE.
- Participant must complete Day 170 of the placebo-controlled part of this study.
Main Exclusion Criteria (placebo-controlled part):
- Participant lives in a skilled nursing facility or dementia care facility.
- Any previous use of experimental therapy within 180 days or 5 half-lives prior to Day 1, whichever is greater. Previous exposure to anti-tau and anti-β-amyloid antibodies is allowed if at the time of screening at least 180 days have passed since the last dose. Previous exposure to amyloid vaccines or tau vaccines meant to treat AD, or previous treatment with oligonucleotides or with gene therapy at any time frame is not allowed.
- Any current or past non-AD neurological conditions.
- Other medical conditions including but not limited to poorly controlled diabetes mellitus, unstable angina, myocardial infarction, chronic heart failure, clinical significant conduction abnormalities, impaired renal or kidney function, which, in the opinion of the Investigator, would make the participant unsuitable for inclusion or could interfere with the participation in or completion of the study.
- 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 the participant is receiving cholinesterase inhibitors and/or memantine, the dose must have been stable within 12 weeks prior to screening, and must remain stable during the duration of the study.
- Brain MRI at screening or within 12 months prior to screening showing evidence of cerebrovascular disease such as acute or sub-acute micro- or macrohemorrhage, significant signs of major cerebrovascular disease, or any other imaging evidence that, in the opinion of the Investigator, makes the participant unsuitable for the study.
Main Exclusion Criteria (OLE part):
- Use of any investigational drugs, or participation in a clinical trial with an investigational new drug (other than NIO752), after completing the initial placebo-controlled part of this trial
- Participants who withdrew informed consent while participating in the main placebo-controlled part of the study
Trial locations and contacts
10 sites in 4 countries.
10 sites in 4 countries
France3 sites
Novartis Investigative Site
Lille, 59037
Novartis Investigative Site
Paris, 75013
Novartis Investigative Site
Toulouse, 31059
Spain3 sites
Novartis Investigative Site
Barcelona, 08036
Novartis Investigative Site
Barcelona, 08041
Novartis Investigative Site
Valencia, Valencia, 46017
Finland2 sites
Novartis Investigative Site
Kuopio, 70210
Novartis Investigative Site
Turku, 20520
Sweden2 sites
Novartis Investigative Site
Malmö, 221 85
Novartis Investigative Site
Stockholm, 141 86
About this study
Official title: A Randomized, Participant and Investigator Blinded, Placebo-Controlled Study to Evaluate the Ability of a Single Intrathecally Administered Dose of NIO752 to Lower Cerebrospinal Fluid Total Tau Levels in Participants With Early Alzheimer's Disease
Phase 1b study to assess the pharmacodynamics, safety, tolerability, and pharmacokinetics of NIO752 in patients with early Alzheimer's disease (AD)
Read the detailed description
This is a phase 1b, randomized, double-blind, placebo-controlled study, in which 36 patients with early AD will be enrolled in one of three cohorts.
Cohorts 1 \& 2 will receive a single intrathecal (IT) dose of NIO752 or placebo in the placebo-controlled part of the study, and multiple administrations of NIO752 in the open-label extension (OLE) part of the study.
Cohort 3 will receive two single IT doses of NIO752 or placebo in the placebo-controlled part of the study, and a single administration of NIO752 in the OLE part of the study.
Each cohort will enroll 12 participants, and they will be randomized into receiving NIO752 or placebo in 2:1 ratio. Participants in cohorts 1\& 2 will remain in this study for approximately ~19 months, including ~18 in-clinic follow up visits during that period of time. In cohort 3, participants will remain in this study for a follow up period of approximately ~18 months including ~10 in-clinic follow up visits.
Cohorts will be enrolled sequentially.
Participants who complete the placebo-controlled part of the study will be eligible to continue in an OLE part of the study regardless of randomization assignment in the placebo-controlled part. All OLE participants will receive either two (cohorts 1 \& 2) or one (cohort 3) dose of NIO752.
Study assessments will include physical and neurological examinations, ECGs, vital signs, standard clinical laboratory evaluations (hematology, blood chemistry, and urinalysis), routine laboratory evaluation of CSF collected through lumbar puncture, adverse event, and serious adverse event monitoring. Cohort 3 participation will also require 3 MRI scans and 3 PET scans throughout the 18 months of the study.
- Conditions
- Alzheimer Disease, Mild Cognitive Impairment
- Being tested
- NIO752, Matching placebo
- Keywords
- Alzheimer Disease, Autosomal dominant Alzheimer disease, Early onset Alzheimer disease, Familial Alzheimer disease, Dementia, Brain Diseases, Central Nervous System Diseases, Nervous System Diseases, Tauopathies, Neurodegenerative Diseases, Neurocognitive Disorders, Memory loss, Placebo, Adult
- Medical subject headings
- Alzheimer Disease, Cognitive Dysfunction, Dementia, Brain Diseases, Central Nervous System Diseases, Nervous System Diseases, Tauopathies, Neurodegenerative Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
NIO752Drug
A single intrathecal (cerebrospinal) injection of NIO752 of Dose A
NIO752Drug
A single intrathecal (cerebrospinal) injection of NIO752 at dose B
Matching placeboDrug
A single intrathecal injection of matching placebo
NIO752Drug
Multiple intrathecal injections of NIO752 of Dose A
NIO752Drug
Two intrathecal injections of NIO752 at dose C
NIO752Drug
Single intrathecal injection of NIO752 at dose C
Matching placeboDrug
Two intrathecal injections of matching placebo
| Study group | Role | What they receive |
|---|---|---|
| NIO752 - Dose A - Cohort 1 | Experimental | A single intrathecal injection of Dose A Receives: Drug: NIO752 |
| Matching placebo - Cohort 1 | Placebo comparator | A single intrathecal injection of artificial cerebrospinal fluid (CSF) Receives: Drug: Matching placebo |
| NIO752 Dose B - Cohort 2 | Experimental | A single intrathecal injection of Dose B Receives: Drug: NIO752 |
| Matching placebo - Cohort 2 | Placebo comparator | A single intrathecal injection of artificial cerebrospinal fluid (CSF) Receives: Drug: Matching placebo |
| NIO752 OLE - Cohorts 1 and 2 | Experimental | Multiple intrathecal injections of Dose A Receives: Drug: NIO752 |
| NIO752 - Dose C - Cohort 3 | Experimental | Two intrathecal injections of Dose C Receives: Drug: NIO752 |
| Matching Placebo - Cohort 3 | Placebo comparator | Two intrathecal injections of artificial cerebrospinal fluid (CSF) Receives: Drug: Matching placebo |
| NIO752 OLE - Cohort 3 | Experimental | Single intrathecal injection of Dose C Receives: Drug: NIO752 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in cerebrospinal total tau from baseline to Day 85
Total tau protein levels in cerebrospinal fluid. More frequent timepoints might be added as deemed necessary per the site Investigator's judgment.
Measured: Baseline, Day 85
Secondary outcomes (7)
Number of adverse events and serious adverse events
Adverse events are assessed at each clinic visit. Laboratory values and other safety assessment values considered clinically significant by the investigator and meet the definition of adverse event will be reported.
Measured: Cohort 1 & 2: Baseline up to 170 days (placebo-controlled part) and up to 589 days (OLE part), Cohort 3: Baseline up to 169 days (placebo-controlled part) and up to 507 days (OLE part)
Concentration of NIO752 in cerebrospinal fluid (CSF)
Concentration of NIO752 in CSF
Measured: Cohorts 1 & 2: Pre-dose, Days 57, 85, 170 (placebo-controlled part) and Days 252, 420, and 588 (OLE part), Cohort 3: Pre-dose, day 1, 57, 85, 169 (placebo-controlled part) and Days 388 and 506 (OLE part)
Cmax, Ctrough in plasma
Maximum and trough level concentrations of NIO752 in plasma
Measured: Cohorts 1, 2 & 3: Pre-dose, 0.5, 1, 2, 3 4, 5, 6, 24 hours post first dose. Cohort 1 & 2: Days 14, 57, 85 and 170 (pbo-controlled part) and 252, 253, 420, 421, and 588 (OLE) Cohort 3: Days 14, 57, 85 and 169 (pbo-controlled part) and 338 and 506 (OLE)
Tmax in blood plasma
Time of Cmax in plasma post-IT injection
Measured: Cohorts 1, 2 & 3: Pre-dose, 0.5, 1, 2, 3 4, 5, 6, 24 hours post first dose. Cohort 1 & 2: Days 14, 57, 85 and 170 (pbo-controlled part) and 252, 253, 420, 421, and 588 (OLE) Cohort 3: Days 14, 57, 85 and 169 (pbo-controlled part) and 338 and 506 (OLE)
AUC-last in blood plasma
Area under curve (AUC) from time zero to the last measurable concentration sampling time (t-last) (mass x time x volume-1)
Measured: Cohorts 1, 2 & 3: Pre-dose, 0.5, 1, 2, 3 4, 5, 6, 24 hours post first dose. Cohort 1 & 2: Days 14, 57, 85 and 170 (pbo-controlled part) and 252, 253, 420, 421, and 588 (OLE) Cohort 3: Days 14, 57, 85 and 169 (pbo-controlled part) and 338 and 506 (OLE)
AUC-inf in blood plasma
The AUC from time zero to infinity (mass x time x volume-1)
Measured: Cohorts 1, 2 & 3: Pre-dose, 0.5, 1, 2, 3 4, 5, 6, 24 hours post first dose. Cohort 1 & 2: Days 14, 57, 85 and 170 (pbo-controlled part) and 252, 253, 420, 421, and 588 (OLE) Cohort 3: Days 14, 57, 85 and 169 (pbo-controlled part) and 338 and 506 (OLE)
Change in CSF total Tau
Evaluating the ability of NIO752 to lower CSF total tau in participants with early AD when administered as multiple doses
Measured: Cohorts 1 & 2: Pre-dose, Days 57, 85, 170 (placebo-controlled part) and Days 252, 420, and 588 (OLE part), Cohort 3: Pre-dose, day 1, 57, 85, 169 (placebo-controlled part) and Days 388 and 506 (OLE part)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Jul 2022
- Study start23 Feb 2023
- Primary completion30 Jul 2026
- Study completion24 Sep 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Alzheimer DiseaseStudies of the same condition, open and under way.
- More trials run by Novartis PharmaceuticalsThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Model description
- Phase 1b
- Masking
- Double blind
- Who is masked
- Participant, Investigator
- Enrolment
- 38 participants (actual)
Sponsor and investigators
- Lead sponsor
- Novartis Pharmaceuticals
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Madhav Thambisetty, MD PhD, Study director, Novartis Pharmaceuticals
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05469360
- Sponsor's protocol ID
- CNIO752B12201
- Other IDs
- 2024-514004-14
- Status last verified
- Sep 2026
- First submitted
- 11 Jul 2022
- Last updated
- 18 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized, Participant and Investigator Blinded, Placebo-Controlled Study to Evaluate the Ability of a Single Intrathecally Administered Dose of NIO752 to Lower Cerebrospinal Fluid Total Tau Levels in Participants With Early Alzheimer's Disease
- ClinicalTrials.gov ID
- NCT05469360
- Acronym / sponsor ID
- CNIO752B12201
- Conditions
- Alzheimer Disease, Mild Cognitive Impairment
- Keywords
- Alzheimer Disease, Autosomal dominant Alzheimer disease, Early onset Alzheimer disease, Familial Alzheimer disease, Dementia, Brain Diseases, Central Nervous System Diseases, Nervous System Diseases
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 38 participants (actual)
- Lead sponsor
- Novartis PharmaceuticalsIndustry (pharma, biotech, devices)
- Study start
- 23 Feb 2023 (actual)
- Primary completion
- 30 Jul 2026 (actual)
- Study completion
- 24 Sep 2027 (estimated)
- First posted
- 21 Jul 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Phase 1b study to assess the pharmacodynamics, safety, tolerability, and pharmacokinetics of NIO752 in patients with early Alzheimer's disease (AD)
Detailed description
This is a phase 1b, randomized, double-blind, placebo-controlled study, in which 36 patients with early AD will be enrolled in one of three cohorts.
Cohorts 1 \& 2 will receive a single intrathecal (IT) dose of NIO752 or placebo in the placebo-controlled part of the study, and multiple administrations of NIO752 in the open-label extension (OLE) part of the study.
Cohort 3 will receive two single IT doses of NIO752 or placebo in the placebo-controlled part of the study, and a single administration of NIO752 in the OLE part of the study.
Each cohort will enroll 12 participants, and they will be randomized into receiving NIO752 or placebo in 2:1 ratio. Participants in cohorts 1\& 2 will remain in this study for approximately ~19 months, including ~18 in-clinic follow up visits during that period of time. In cohort 3, participants will remain in this study for a follow up period of approximately ~18 months including ~10 in-clinic follow up visits.
Cohorts will be enrolled sequentially.
Participants who complete the placebo-controlled part of the study will be eligible to continue in an OLE part of the study regardless of randomization assignment in the placebo-controlled part. All OLE participants will receive either two (cohorts 1 \& 2) or one (cohort 3) dose of NIO752.
Study assessments will include physical and neurological examinations, ECGs, vital signs, standard clinical laboratory evaluations (hematology, blood chemistry, and urinalysis), routine laboratory evaluation of CSF collected through lumbar puncture, adverse event, and serious adverse event monitoring. Cohort 3 participation will also require 3 MRI scans and 3 PET scans throughout the 18 months of the study.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Sequential
- Masking
- Double blind (participant, investigator)
- Number of arms
- 8
- Model description
- Phase 1b
| Arm | Type | Receives |
|---|---|---|
| NIO752 - Dose A - Cohort 1 | Experimental | Drug: NIO752A single intrathecal injection of Dose A |
| Matching placebo - Cohort 1 | Placebo comparator | Drug: Matching placeboA single intrathecal injection of artificial cerebrospinal fluid (CSF) |
| NIO752 Dose B - Cohort 2 | Experimental | Drug: NIO752A single intrathecal injection of Dose B |
| Matching placebo - Cohort 2 | Placebo comparator | Drug: Matching placeboA single intrathecal injection of artificial cerebrospinal fluid (CSF) |
| NIO752 OLE - Cohorts 1 and 2 | Experimental | Drug: NIO752Multiple intrathecal injections of Dose A |
| NIO752 - Dose C - Cohort 3 | Experimental | Drug: NIO752Two intrathecal injections of Dose C |
| Matching Placebo - Cohort 3 | Placebo comparator | Drug: Matching placeboTwo intrathecal injections of artificial cerebrospinal fluid (CSF) |
| NIO752 OLE - Cohort 3 | Experimental | Drug: NIO752Single intrathecal injection of Dose C |
Who may qualify
- Ages
- 30 to 74 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| NIO752A single intrathecal (cerebrospinal) injection of NIO752 of Dose A | Drug | NIO752 - Dose A - Cohort 1 |
| NIO752A single intrathecal (cerebrospinal) injection of NIO752 at dose B | Drug | NIO752 Dose B - Cohort 2 |
| Matching placeboA single intrathecal injection of matching placebo | Drug | Matching placebo - Cohort 1, Matching placebo - Cohort 2 |
| NIO752Multiple intrathecal injections of NIO752 of Dose A | Drug | NIO752 OLE - Cohorts 1 and 2 |
| NIO752Two intrathecal injections of NIO752 at dose C | Drug | NIO752 - Dose C - Cohort 3 |
| NIO752Single intrathecal injection of NIO752 at dose C | Drug | NIO752 OLE - Cohort 3 |
| Matching placeboTwo intrathecal injections of matching placebo | Drug | Matching Placebo - Cohort 3 |
Primary outcome
Change in cerebrospinal total tau from baseline to Day 85
Time frame: Baseline, Day 85
Total tau protein levels in cerebrospinal fluid. More frequent timepoints might be added as deemed necessary per the site Investigator's judgment.
7 secondary outcomes
Number of adverse events and serious adverse events
Time frame: Cohort 1 & 2: Baseline up to 170 days (placebo-controlled part) and up to 589 days (OLE part), Cohort 3: Baseline up to 169 days (placebo-controlled part) and up to 507 days (OLE part)
Concentration of NIO752 in cerebrospinal fluid (CSF)
Time frame: Cohorts 1 & 2: Pre-dose, Days 57, 85, 170 (placebo-controlled part) and Days 252, 420, and 588 (OLE part), Cohort 3: Pre-dose, day 1, 57, 85, 169 (placebo-controlled part) and Days 388 and 506 (OLE part)
Cmax, Ctrough in plasma
Time frame: Cohorts 1, 2 & 3: Pre-dose, 0.5, 1, 2, 3 4, 5, 6, 24 hours post first dose. Cohort 1 & 2: Days 14, 57, 85 and 170 (pbo-controlled part) and 252, 253, 420, 421, and 588 (OLE) Cohort 3: Days 14, 57, 85 and 169 (pbo-controlled part) and 338 and 506 (OLE)
Tmax in blood plasma
Time frame: Cohorts 1, 2 & 3: Pre-dose, 0.5, 1, 2, 3 4, 5, 6, 24 hours post first dose. Cohort 1 & 2: Days 14, 57, 85 and 170 (pbo-controlled part) and 252, 253, 420, 421, and 588 (OLE) Cohort 3: Days 14, 57, 85 and 169 (pbo-controlled part) and 338 and 506 (OLE)
AUC-last in blood plasma
Time frame: Cohorts 1, 2 & 3: Pre-dose, 0.5, 1, 2, 3 4, 5, 6, 24 hours post first dose. Cohort 1 & 2: Days 14, 57, 85 and 170 (pbo-controlled part) and 252, 253, 420, 421, and 588 (OLE) Cohort 3: Days 14, 57, 85 and 169 (pbo-controlled part) and 338 and 506 (OLE)
AUC-inf in blood plasma
Time frame: Cohorts 1, 2 & 3: Pre-dose, 0.5, 1, 2, 3 4, 5, 6, 24 hours post first dose. Cohort 1 & 2: Days 14, 57, 85 and 170 (pbo-controlled part) and 252, 253, 420, 421, and 588 (OLE) Cohort 3: Days 14, 57, 85 and 169 (pbo-controlled part) and 338 and 506 (OLE)
Change in CSF total Tau
Time frame: Cohorts 1 & 2: Pre-dose, Days 57, 85, 170 (placebo-controlled part) and Days 252, 420, and 588 (OLE part), Cohort 3: Pre-dose, day 1, 57, 85, 169 (placebo-controlled part) and Days 388 and 506 (OLE part)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Sep 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Madhav Thambisetty, MD PhD study director
Novartis Pharmaceuticals
10 sites in 4 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing NIO752 in people with Alzheimer Disease and Mild Cognitive Impairment, run by Novartis Pharmaceuticals at 10 sites in 4 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 18 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 10 sites in France, Spain, Finland, Sweden. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in cerebrospinal total tau from baseline to Day 85 (time frame: Baseline, Day 85). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Sep 2026.