2-Hydroxybenzylamine (2-HOBA) Study in Early Alzheimer's Patients

NCT ID: NCT06432166

Last Updated: 2025-05-08

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 48 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-09-01
• Study Completion Date: 2028-12-31

Brief Summary

Investigators propose a phase 1b/2a, randomized, double-blind, placebo-controlled, parallel group dose finding and biomarker study to evaluate the safety, tolerability, and biomarker activity of 2-HOBA in 48 MCI/AD participants. Participants will be randomized 1:1:1:1 to receive 250, 500, 750 mg 2-HOBA acetate TID or placebo for 16 weeks. Blood and cerebral spinal fluid (CSF) will be collected to measure markers of protein modification by dicarbonyls (IsoLGs- & MDA), pTau-181, YKL-40, and NF-L.

Detailed Description

This is a phase 1b/2a, randomized, double-blind, placebo-controlled, parallel group dose finding and biomarker study to evaluate the safety, tolerability, and biomarker activity of 2-HOBA in 48 MCI/AD participants. Participants will be randomized 1:1:1:1 to receive 250, 500, 750 mg 2-HOBA acetate TID or placebo for 16 weeks. Blood and CSF will be collected to measure markers of protein modification by dicarbonyls (IsoLGs- & MDA), pTau-181, YKL-40, and NF-L. Investigators anticipate screening 120 subjects to randomize up to 60 subjects with the goal of 48 patients completing the study (allowing for up to 25% dropout) for the 16-week study.

The primary aims of this project are to 1) Provide proof-of-concept that 2-HOBA protects proteins from covalent modification by inhibiting lysine-reacting dicarbonyls in the human brain. Investigators hypothesize that 16 weeks of 2-HOBA treatment will significantly reduce CSF levels of the dilysyl-MDA and IsoLG adduct of CSF proteins in a dose-responsive relationship. 2) Evaluate whether 2-HOBA is safe for extended use in patients with early AD. Investigators hypothesize that 2-HOBA will be safe and well tolerated through 16 weeks of use. Tolerability will be assessed by monitoring symptoms, adverse events, vital signs, ECG, and safety labs during the study.

The secondary aims are to evaluate the effect of 2-HOBA treatment on AD biomarkers, brain inflammation, disease severity, and cognitive performance.

Conditions

Alzheimer Disease; Mild Cognitive Impairment

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Placebo

Placebo treatment TID for 16 weeks.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Placebo taken three times per day for 16 weeks.

250 mg 2-HOBA acetate

250 mg of 2-hydroxybenzylamine (2-HOBA) acetate TID for 16 weeks.

Group Type: ACTIVE_COMPARATOR

2-hydroxybenzylamine acetate

Intervention Type: DRUG

2-hydroxybenzylamine acetate (2-HOBA) is taken three times per day for 16 weeks

500 mg 2-HOBA acetate

500 mg of 2-hydroxybenzylamine (2-HOBA) acetate TID for 16 weeks.

Group Type: ACTIVE_COMPARATOR

2-hydroxybenzylamine acetate

Intervention Type: DRUG

2-hydroxybenzylamine acetate (2-HOBA) is taken three times per day for 16 weeks

750 mg 2-HOBA acetate

750 mg of 2-hydroxybenzylamine (2-HOBA) acetate TID for 16 weeks.

Group Type: ACTIVE_COMPARATOR

2-hydroxybenzylamine acetate

Intervention Type: DRUG

2-hydroxybenzylamine acetate (2-HOBA) is taken three times per day for 16 weeks

Interventions

2-hydroxybenzylamine acetate

2-hydroxybenzylamine acetate (2-HOBA) is taken three times per day for 16 weeks

Intervention Type: DRUG

Placebo

Placebo taken three times per day for 16 weeks.

Intervention Type: OTHER

Other Intervention Names

2-HOBA

Eligibility Criteria

Inclusion Criteria

MCI due to AD:

1. Male or female, aged 55-85 years (both inclusive) at the time of signing informed consent.

2. Participant must have a subjective memory concern as reported by participant, study partner, or clinician.

3. Mini-Mental State Exam31 score between 24 and 30, inclusive

4. Clinical Dementia Rating (CDR)32 Global = 0.5. Memory Box score must be at least 0.5.

Mild AD:

1. Male or female, aged 55-85 years (both inclusive) at the time of signing informed consent.

2. Mild dementia of the Alzheimer's type according to the NIA-AA 2018 criteria.

3. CDR global score of 0.5 and CDR of 0.5 or more in at least one of the three instrumental activities of daily living categories (personal care, home & hobbies, community affairs) Or CDR global score of 1.0

4. MMSE ≥20

1. Age 55-85 (inclusive)

2. Abnormal memory function documented by scoring within the education adjusted ranges on the Logical Memory II subscale (Delayed Paragraph Recall) from the Wechsler Memory Scale - Revised:

• Less than or equal to 11 for 16 or more years of education
• Less than or equal to 9 for 8 - 15 years of education
• Less than or equal to 6 for 0 - 7 years of education

3. Amyloid positivity established using the C2N Precivity2 Plasma test (Aβ42/40 plus p- tau217/np-tau217. (This test uses a statistical algorithm to integrate a patient's Aβ42/40 Ratio and p-Tau217 Ratio to calculate the Amyloid Probability Score 2 (APS2) and determines whether a patient is positive or negative for brain amyloid deposition based on a binary cutoff value).

4. Stable permitted medications for 4 weeks or longer as specified in Section 4.6.3, including:

a. Memantine and cholinesterase inhibitors are allowable if stable for 12 weeks prior to screen.

5. Geriatric Depression Scale33 score of less than or equal to 14.

6. Study Partner is available who has frequent contact with the participant (e.g., an average of 10 hours per week or more) and can accompany the participant to most visits to answer questions about the participant.

7. Adequate visual and auditory acuity to allow neuropsychological testing.

8. Good general health with no additional diseases/disorders expected to interfere with the study.

9. Participant is not pregnant, lactating, or of childbearing potential (i.e., women must be two years post-menopausal or surgically sterile).

10. Completed six grades of education or has a good work history.

11. Must speak English fluently.

12. Provide written informed consent. Participants must have the capacity to consent.

Exclusion Criteria

1. Any other significant neurologic disease including Parkinson's disease, multi- infarct dementia, Huntington's disease, normal pressure hydrocephalus, brain tumor, progressive supranuclear palsy, seizure disorder, subdural hematoma, multiple sclerosis, or history of significant head trauma followed by persistent neurologic deficits or known structural brain abnormalities.

2. Major depression, bipolar disorder as described in DSM-V within the past 1 year or psychotic features, agitation, or behavioral problems within 3 months, which could lead to difficulty complying with the protocol.

3. History of schizophrenia (DSM V criteria).

4. History of alcohol or substance abuse or dependence within the past 2 years (DSM V criteria).

5. Clinically significant or unstable medical condition, including uncontrolled hypertension, uncontrolled diabetes, or significant cardiac, pulmonary, renal, hepatic (Class C defined by Child-Pugh criteria), endocrine, or other systemic disease in the opinion of the Investigator, may either put the participant at risk because of participation in the study, or influence the results, or the participant's ability to participate in the study.

6. Has had a history within the last 5 years of a primary or recurrent malignant disease with the exception of non-melanoma skin cancers, resected cutaneous squamous cell carcinoma in situ, basal cell carcinoma, cervical carcinoma in situ, or in situ prostate cancer with normal prostate-specific antigen post-treatment.

7. Clinically significant abnormalities in B12 or TFTs that might interfere with the study. A low B12 is exclusionary, unless the required follow-up labs (homocysteine (HC) and methylmalonic acid (MMA) indicate that it is not physiologically significant.

8. Clinically significant abnormalities in screening laboratories or ECG.

9. Residence in a skilled nursing facility.

10. Use of any excluded medication as described in Section 6.10, including:

• Use centrally acting anti-cholinergic drugs.
• Use of any investigational drugs within 4 weeks or 5 half-lives, whichever is longer, prior to screening.

11. A current blood clotting or bleeding disorder, or significantly abnormal PT or PTT at screening.

12. Contraindications for MRI studies, including claustrophobia, the presence of metal(ferromagnetic) implants, or cardiac pacemaker.

13. Participants whom the Site PI deems to be otherwise ineligible.

• Minimum Eligible Age: 55 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Vanderbilt University Medical Center

OTHER

Sponsor Role: collaborator

MTI Biotech Inc

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Paul Newhouse, M.D.

Role: PRINCIPAL_INVESTIGATOR

Vanderbilt University Medical Center

John A. Rathmacher, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

MTI Biotech Inc

Locations

Center for Cognitive Medicine, Vanderbilt University Medical Center

Nashville, Tennessee, United States

Countries

United States

Central Contacts

John A. Rathmacher, Ph.D.

Role: CONTACT

rathmacher@mtibiotech.com

515-296-9916

Facility Contacts

Amy R Boegel, Ph.D.

Role: primary

amy.r.boegel@vumc.org

(615) 875-0955

Other Identifiers

RC-201910-2019696

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

IRB 231544

Identifier Type: OTHER

Identifier Source: secondary_id

MTI2024-CS01

Identifier Type: -

Identifier Source: org_study_id