DISCOVER: Safety, Tolerability, PK and PD of Posiphen® in Subjects With Early Alzheimer's Disease

Sponsor

Annovis Bio Inc. (Industry)

Overall Status

Active, not recruiting

CT.gov ID

NCT02925650

Collaborator

Alzheimer's Disease Cooperative Study (ADCS) (Other)

Enrollment

Locations

Arms

Anticipated Duration (Months)

3.2

Patients Per Site

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This study evaluates the safety and pharmacological effects of 3 different doses of Posiphen® when compared to a placebo, in adult male and female patients with early Alzheimer's disease (AD).

Condition or Disease	Intervention/Treatment	Phase
Alzheimer's Disease	Drug: Posiphen Drug: Placebo	Phase 1/Phase 2

Detailed Description

Posiphen®, which was discovered by the US National Institute on Aging (NIA) is a small, orally active, experimental drug that specifically inhibits the synthesis of amyloid precursor protein (APP), Tau and α-Synuclein. It is distinct from other Alzheimer's disease drugs currently in development, because it inhibits the formation of several toxic proteins, rather than removing individual toxic protein after they are produced. Posiphen has potential utility as a disease modifying treatment for AD. The present study will confirm the pharmacokinetics (PK) of Posiphen and its metabolites in plasma and cerebral spinal fluid (CSF). It will also measure the effects of a 23-25 day treatment period with Posiphen on the CSF and plasma levels of a number of biomarkers, inflammatory factors and control proteins. It will also expand the safety data in humans by extending the treatment period from 10 days to a treatment period from 23-25 days. In addition, this study will measure concentrations of various soluble biomarkers in CSF and use the SILK™ assay methods to directly measure the effect of Posiphen on the fractional synthesis rate of Aβ40 in CSF, which will help guide the further development of Posiphen and determine the feasibility of SILK™ in a multicenter trial.

Study Design

Study Type:

Interventional

Actual Enrollment :

19 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Primary Purpose:

Treatment

Official Title:

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamic (PD) Effects of Posiphen® in Subjects With Early Alzheimer's Disease (AD)

Actual Study Start Date :

Mar 2, 2017

Actual Primary Completion Date :

Dec 31, 2021

Anticipated Study Completion Date :

Dec 31, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Low Dose The study drug Posiphen dosage of 60mg is to be taken orally in divided doses, three times per day for a total 23-25 days.	Drug: Posiphen oral solid dosage form capsule
Experimental: Medium Dose The study drug Posiphen dosage of 120mg is to be taken orally in divided doses, three times per day for a total 23-25 days.	Drug: Posiphen oral solid dosage form capsule
Experimental: High Dose The study drug Posiphen dosage of 180mg is to be taken orally in divided doses, three times per day for a total 23-25 days.	Drug: Posiphen oral solid dosage form capsule
Placebo Comparator: Placebo The Placebo comparator is to be taken orally in divided doses, three times per day for a total 23-25 days.	Drug: Placebo oral solid dosage form capsule

Outcome Measures

Primary Outcome Measures

Safety and Tolerability of multiple ascending doses of Posiphen: Reports of adverse events or study discontinuations [Up to 25 days]
Reports of adverse events or study discontinuations related to Posiphen
The levels of Posiphen and its metabolites will be determined in plasma [Up to 25 days]
Mean plasma concentrations of levels of posiphen tartrate, N1 desmethyl posiphen , and N8 desmethyl Posiphen metabolite will be determined for each of the three dose cohorts (posiphen 60 mg, 120 mg, 180 mg)
The levels of Posiphen and its metabolites will be determined in cerebrospinal fluid (CSF) [Up to 25 days]
Mean cerebrospinal fluid concentrations of posiphen tartrate, and N1 desmethyl posiphen, and N8 desmethyl pospiphen will be determined for each of the three dose cohorts (posiphen 60 mg, 120 mg, 180 mg)
Fractional synthesis rate of Aβ40 in CSF using the SILK™ technique with multiple doses of Posiphen [Up to 25 days]
The fractional synthesis rate (FSR) of Aβ40 will be measured in the CSF using the SILK™ technique

Secondary Outcome Measures

Feasibility of CSF catheter study with SILK™ technology to evaluate rates of enrollment [Up to 25 days]
Enrollment rates will be evaluated across participating sites.
Feasibility of CSF catheter study with SILK™ technology to evaluate %CSF samples with enough volume for testing [Up to 25 days]
The % of cerebrospinal fluid samples with sufficient volume for testing will be determined across study participants during the SILK sampling procedure
Feasibility of CSF catheter study with SILK™ technology to evaluate research satisfaction [Up to 25 days]
Research satisfaction will be evaluated by qualitative response to 14 questions asked to participants about their experience with the study procedures. Responses will be grouped and reported by common themes
Pharmacodynamic and PK-PD effects on CSF Alzheimer's Disease Biomarkers [Up to 25 days]
Alzheimer's Disease biomarkers including Beta Amyloid 38 (Aβ38), Aβ40, Aβ42, Soluble Amyloid Precursor Protein alpha (sAPPα), Soluble Amyloid Precursor Protein beta (sAPPβ), and T-Tau, will be measured in the CSF to determine if Posiphen has an effect on their levels.
Assessment of mental status effects [Up to 25 days]
The short-term effects of Posiphen on mental status will be measured using the Mini-Mental State Examination (MMSE).
Assessment of neuropsychiatric effects [Up to 25 days]
The short-term effects of Posiphen on neuropsychiatric symptoms will be measured using the Neuropsychiatric Inventory (NPI).
Assessment of cognitive effects [Up to 25 days]
The short-term effects of Posiphen on cognition will be measured using the Alzheimer's Disease Assessment Scale (ADAS-Cog12).

Other Outcome Measures

Fractional synthesis rates with normalized SILK curve sampling [Up to 25 days]
Exploratory analyses of the fractional synthesized rates with normalized SILK curve sampling; of Aβ38, Aβ42, Total Aβ, and ratio curve of Aβ42/40.
Absolute synthesis and clearance rates [Up to 25 days]
Measurements of newly generated Aβ38, Aβ40, Aβ42, Total Aβ, and ratio of Aβ42/40.

Eligibility Criteria

Criteria

Ages Eligible for Study:

55 Years to 89 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male or female aged 55 to 89 years (inclusive), in good health, no frailty.
Female participants must be post-menopausal for at least 2 consecutive years or surgically sterile (bilateral tubal ligation, hysterectomy or bilateral oophorectomy) for at least 6 months prior to screening.
Female participants will be given a urine pregnancy test at the screening visit for which they should test negative.
Clinical profile consistent with MCI or mild AD, consistent with the core clinical criteria outlined in the NIA-AA Guidelines (2011).
MMSE score between 17 and 30 (inclusive).
CDR global score of 0.5 with a memory score of 0.5 or greater, or CDR global score of 1.0.
Participant likely to tolerate all study procedures per PI judgment.
To qualify for entry, subjects will have a CSF Abeta42-Abeta40 ratio below 0.131 that is consistent with Alzheimers disease as measured via mass spectrometry by C2N.
General cognition and functional performance sufficiently preserved that the subject can provide written informed consent.
A minimum of 6 years of education or good work history.
Study partner is available who has frequent contact with the subject (e.g., average of 10 hours per week or more), and can accompany the subject to most visits to answer questions about the subject. The study partner is required to attend the entire screening visit and the baseline visit. The study drug is dispensed to the participant at the baseline visit and the study partner (or other individual) should also oversee study drug administration if needed to ensure compliance with dose regimen. At a minimum, the study partner should stay for the first 3 hours of the confinement visit and return at the discharge to drive the subject home.
No evidence of current suicidal ideation or previous suicide attempt in the past month as evaluated in the Columbia Suicide Severity Rating Scale.
MRI scan within the 12 months prior to screening without evidence of infection, infarction, or other focal lesions and without clinical symptoms suggestive of intervening neurological disease. Lacunes that are not believed to contribute to the subjects cognitive impairment are permissible. If there is no MRI available within a 12-month timeframe, then an MRI must be performed as part of the screening procedures for eligibility.
Stability of permitted medications for 4 weeks prior to baseline. NOTE: Cholinesterase inhibitors and or memantine are allowable only if stable for 12 weeks prior to screen. If taking Arciept (donezepil), no more than 10 mg/day is permitted during the course of the study.
Adequate visual and hearing ability (physical ability to perform all the study assessments).
Good general health with no disease expected to interfere with the study. Subjects may have common age-related disorders (i.e., hypertension, type II diabetes, dyslipidemia, and hypothyroidism) as long as these disorders are being controlled by diet or medication.
Must speak English, Spanish, or Korean fluently.

Exclusion Criteria:

Has a history of a psychiatric disorder such as schizophrenia, bipolar disorder or major depression according to the criteria of the most current version of the Diagnostic and Statistical Manual of Mental Disorders (DSM). Mild depression or history of depression that is stable on treatment with a tricyclic antidepressant SSRI or SNRI medication at a stable dose is acceptable.
Other neurodegenerative diseases, including Parkinsons disease and Huntingtons disease, or cerebral tumor.
Dementia other than AD, such as Acquired Immunodeficiency Syndrome (AIDS), Creutzfeldt-Jakob disease (CJD), Lewy Bodies dementia (LBD), Cerebrovascular dementia (CVD), Progressive Supranuclear Palsy (PSP), or normal pressure hydrocephalus (NPH).
History of a seizure disorder.
Clinically significant abnormalities in screening laboratory or ECG results.
Has current serious or unstable illness including cardiovascular, hepatic, renal, gastroenterologic, respiratory, endocrinologic, neurologic, psychiatric, immunologic, or hematologic disease or other conditions that, in the investigators opinion, makes them ineligible for participation in this study.
Has four or more microinfarcts as noted in the MRI scan.
Has cancer or has had a malignant tumor within the past 3 years, except patients who underwent potentially curative therapy with no evidence of recurrence. (Patients with stable untreated prostate cancer or skin cancers are not excluded).
According to the criteria of the most current version of the DSM, alcohol abuse, alcohol dependence, or drug abuse in the past 5 years.
Participation in another clinical trial with an investigational agent and have taken at least one dose of study medication, unless unblinded on placebo, within 16 weeks prior to screening. (The end of a previous investigational trial is the date the last dose of an investigational agent was taken).
Resides in a skilled nursing facility.
Subjects with infection or inflammation of the skin or skin disease at or in proximity to the lumbar puncture site.
History of lumbar spine surgery or chronic low back pain (CLBP).
Subjects whom the site PI deems to be otherwise ineligible.
Has a deep brain stimulator (DBS).

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	UCSD Alzheimer's Disease Research Center	La Jolla	California	United States	92037
2	IU Health Partners, Adult Neurology Clinic	Indianapolis	Indiana	United States	46202
3	Johns Hopkins Hospital	Baltimore	Maryland	United States	21287
4	Washington University Sleep Medicine Center	Brentwood	Missouri	United States	63144
5	Columbia University Medical Center Sergievsky Center Taub Institute	New York	New York	United States	10032
6	Cleveland Clinic	Cleveland	Ohio	United States	44195