- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07611396
Crownlands Observing Progression With Neurons Study (CROWN-I)
Crownlands Observing Progression With Neurons I (CROWN-I)
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
Neurological diseases are difficult to characterize at the molecular level because disease-relevant tissue is rarely available in clinical practice. As a result, precision approaches in neurology have historically relied on indirect measures, including clinical assessments, neuroimaging, and biomarkers measured in blood, cerebrospinal fluid (CSF), and other biofluids. Although these tools have advanced diagnosis and monitoring, they provide limited access to neuron-specific and high-dimensional molecular information.
CROWN-I is a data-intensive longitudinal observational study designed to expand molecular and clinical characterization of Alzheimer's disease (AD) and mild cognitive impairment (MCI). The CROWN-I Study aims to track multiple high-dimensional molecular readouts in participants with AD and MCI as well as cognitively normal controls (CN). Participants will provide biospecimens at multiple time points and complete medical histories and clinical and cognitive assessments.
The study will analyze molecular signatures from olfactory neuron samples and blood. These data will be used to differentiate participant subgroups and may inform new therapeutic and clinical strategies for disease-modifying medicines.
Undersøgelsestype
Tilmelding (Anslået)
Kontakter og lokationer
Studiekontakt
- Navn: Mason Sanfilippo, MS
- Telefonnummer: (415) 623-8635
- E-mail: m.sanfilippo@crownlands.com
Studiesteder
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Maryland
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Germantown, Maryland, Forenede Stater, 20876
- Rekruttering
- Capital Neurology
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Informed consent provided by the participant or, where applicable, Legally Authorized Representative (LAR) or other substitute decision-maker where permitted by applicable law, as described in Section 8.2.
- Male or female, age ≥ 55 years at Screening.
- Fluency of subject and study partner in English sufficient to complete all cognitive and self-report assessments without interpreter assistance.
- Adequate visual and auditory acuity (with correction permitted) sufficient to complete neuropsychological testing.
- Not pregnant or lactating.
- Medications stable ≥ 4 weeks before screening.
- GDS-15 < 6 (i.e., 0-5 inclusive; no current significant depression).
- Available study partner who has known the participant for ≥ 12 months, maintains ~10+ hours per week of in-person or telephone contact, and is willing to attend study visits and complete informant-rated assessments.
- Willing to complete olfactory brushing, smell testing, and venous blood draw.
- Willing to commit to baseline and follow-up visits across study duration.
- In the opinion of the Investigator, able to comply with the protocol-specified visit schedule and procedures for the full study duration.
Exclusion Criteria:
- Current or active clinically significant neurological disorder (in the opinion of the Investigator) other than the disorders in the study arms, including but not limited to:
- Parkinson's disease, dementia with Lewy bodies, frontotemporal dementia, progressive supranuclear palsy, corticobasal degeneration, Huntington's disease, prion disease, multi-infarct dementia, normal pressure hydrocephalus, brain tumor, seizure disorder, subdural hematoma, multiple sclerosis, significant head trauma with persistent deficits, or known structural brain abnormalities.
- Active or unstable major psychiatric illness (DSM-5 schizophrenia spectrum, bipolar I, or severe major depressive disorder with active suicidality) within 6 months prior to Screening; history of schizophrenia at any time.
- Psychotic features, agitation, or behavioral problems within the last 3 months that could interfere with protocol compliance.
- Current substance use disorder (DSM-5 moderate or severe), or alcohol use disorder within 24 months prior to Screening.
- Active malignancy under treatment, or malignancy with expected survival < 30 months (excluding non-melanoma skin cancer and localized prostate cancer on active surveillance).
- Participation in studies collecting neuropsychological measures more than once per year.
- Presence of previous nasal surgery or other anatomical abnormalities that could interfere with the procedure on both sides of the nose, at the discretion of the clinician administering the Olfactory Brushing.
- Active respiratory infection or recent history of respiratory infection within the past two weeks.
- Known allergy or adverse reaction to topical anesthetics or decongestants used in the study (e.g., lidocaine, tetracaine, oxymetazoline).
- Any other medical or psychiatric condition or lab abnormality that, in the opinion of the Investigator, might preclude participation or render the participant unsuitable for study enrollment.
Cognitively Normal (CN) Additional Inclusion Criteria (CN)
- No subjective cognitive complaint reported by participant AND no cognitive -complaint reported by study partner.
- No current or prior clinical diagnosis of MCI, Alzheimer's disease, or any other dementia, and no current clinical diagnosis of a neurological or neuropsychiatric disease.
- MMSE score ≥ 27 / 30 at Screening.
- Global Clinical Dementia Rating (CDR) = 0 at Screening.
- CDR Sum of Boxes (CDR-SB) = 0 at Screening.
- Performance within 1.0 standard deviation of demographically adjusted norms on the Rey Auditory Verbal Learning Test (RAVLT) Delayed Recall.
Additional Exclusion Criteria (CN)
- Current or prior use of cholinesterase inhibitors (donepezil, rivastigmine, galantamine) or memantine for any indication.
- Current or prior use of anti-amyloid monoclonal antibody disease-modifying therapy (aducanumab, lecanemab, donanemab, or any investigational anti-amyloid mAb).
Mild Cognitive Impairment (MCI) Additional Inclusion Criteria (MCI)
- Subjective cognitive complaint reported by participant OR partner-verified memory complaint reported by study partner.
- MMSE score ≥ 24 and ≤ 30 at Screening.
- Global CDR = 0.5 at Screening.
- CDR-SB ≥ 0.5 and < 3 at Screening; CDR Memory Box ≥ 0.5.
- Performance ≥ 1.5 standard deviations below demographically adjusted norms on the RAVLT Delayed Recall (or equivalent episodic memory criterion per the Petersen / NIA-AA MCI framework).
- Preserved general functional ability such that the participant does not meet criteria for dementia (i.e., does not meet AD criteria in Section 7.3).
Alzheimer's Disease (AD) Additional Inclusion Criteria (AD)
- Confirmed clinical diagnosis of probable Alzheimer's disease by a qualified specialist (cognitive neurologist, geriatric psychiatrist, or equivalent), consistent with NIA-AA 2011 (McKhann et al.) or NIA-AA 2018 Research Framework biological criteria.
- MMSE score ≥ 16 and ≤ 26 at Screening.
- Global CDR ≥ 1 at Screening.
- CDR-SB ≥ 3 at Screening.
- CDR Memory Box score ≥ 0.5 at Screening.
- Partner-verified history of progressive cognitive decline of ≥ 6 months duration.
- Functional impairment consistent with dementia, as documented on the CDR Functional Domains (Community Affairs, Home & Hobbies, Personal Care); participant able to complete protocol.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
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Alzheimer's disease (AD)
Participants with diagnosed Alzheimer's disease
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Mild cognitive impairment (MCI)
Participants with diagnosed or apparent MCI
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Cognitively normal
Participants who are cognitively normal
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Rate of change in CDR-SB
Tidsramme: From enrollment to the end of the observational period at 18 months or final visit
|
The primary clinical outcomes are longitudinal changes from baseline in Clinical Dementia Rating - Sum of Boxes as administered by a qualified clinician.
The CDR-SB evaluates six domains (memory, orientation, judgment, community affairs, home/hobbies, and personal care) for a total score ranging from 0 to 18, with increases indicating worsening impairment.
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From enrollment to the end of the observational period at 18 months or final visit
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Change in olfactory neuron transcriptomic profile
Tidsramme: From enrollment to the end of the observational period at 18 months or final visit
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Change from baseline in olfactory neurons measured by Gateway in transcriptomic pathways associated with AD by human genetics.
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From enrollment to the end of the observational period at 18 months or final visit
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in p-tau217 in blood plasma
Tidsramme: From enrollment to the end of the observational period at 18 months or final visit
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Change in quantitative levels of p-tau217 in blood plasma over the study observational period.
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From enrollment to the end of the observational period at 18 months or final visit
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Change in Aβ42/Aβ40 in blood plasma
Tidsramme: From enrollment to the end of the observational period at 18 months or final visit
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Change in quantitative levels of amyloid β-peptide (Aβ) 42 : amyloid β-peptide (Aβ) 40 ratio in blood plasma over the study observational period.
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From enrollment to the end of the observational period at 18 months or final visit
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Change in whole blood transcriptomic profile
Tidsramme: From enrollment to the end of the observational period at 18 months or other endpoint
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Change from baseline in transcriptomic pathways associated with AD by human genetics in whole blood.
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From enrollment to the end of the observational period at 18 months or other endpoint
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Change in plasma proteomic profile
Tidsramme: From enrollment to the end of the observational period at 18 months or other endpoint
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Change from baseline in proteomic pathways associated with AD in plasma.
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From enrollment to the end of the observational period at 18 months or other endpoint
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Cross-sectional differences in olfactory neuron transcriptomics
Tidsramme: Baseline
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Difference between participants in different cohorts in olfactory neurons measured by Gateway in transcriptomic pathways associated with AD by human genetics.
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Baseline
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Change in clinical diagnosis
Tidsramme: From enrollment to the end of the observational period at 18 months or final visit
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Measuring new clinical diagnoses of MCI and/or AD in participants without the diagnosis at the first visit
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From enrollment to the end of the observational period at 18 months or final visit
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Rate of change in MMSE
Tidsramme: From enrollment to the end of the observational period at 18 months or final visit
|
A secondary outcome is longitudinal changes from baseline in Mini-Mental State Examination, a 30-point evaluation where lower scores indicate cognitive worsening.
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From enrollment to the end of the observational period at 18 months or final visit
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Rate of change on RAVLT
Tidsramme: From enrollment to the end of the observational period at 18 months or final visit
|
A secondary outcome is longitudinal changes from baseline in Rey Auditory Verbal Learning Test, an assessment where lower scores indicate worsening episodic memory.
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From enrollment to the end of the observational period at 18 months or final visit
|
Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- CLNDS-16530
Plan for individuelle deltagerdata (IPD)
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