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Active not recruitingPhase 2 / PHASE3

Piromelatine 20 mg in Participants With Mild Dementia Due to Alzheimer's Disease

Randomized, Delayed Start, Double Blind, Parallel Group, Placebo Controlled, Multicenter Study of Piromelatine 20 mg in Participants With Mild Dementia Due to Alzheimer's Disease

Asset

Piromelatine

Listed sites

37

Recruiting sites

-

Enrollment

225

estimated

Study population

Alzheimer’s disease

Key I/E criteria

•Alzheimer's disease•MMSE 20•Study partner/caregiver required

Primary endpoint

•ADAS-Cog

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT05267535
Org study IDNEUP11-7

Timeline

Milestones

Study first posted2022-03-04actual
Study start2022-05-12actual
Last update posted2024-06-21actual
Primary completion2025-06estimated (month precision)
Study completion2025-06estimated (month precision)

Assets

Drug assets

Piromelatine

Study populations

Who this study enrolls

Alzheimer’s disease

Eligibility

Who can enroll

Minimum age60 Years
Maximum age85 Years
SexAll
Healthy volunteersNot accepted

Inclusion criteria

•Male or female aged 60 85 years (inclusive).
•Participant is an outpatient living at home or in an assisted living facility and is willing to attend all planned visits during the study.
•The participant has a study partner (who is not expected to change during the study) who will accompany the patient to the clinic, and/or be available by telephone at designated times, monitor administration of prescribed medications, control the minimum 2 hour daily light exposure requirement. The study partner must, in the opinion of the investigator, have enough contact with the participant to be able to perform the duties described above.
•Signed informed consent from the patient who has the capacity to provide informed consent as judged by the study investigator
•Signed informed consent from the study partner.
•Meets NIA AA research criteria for probable AD (McKhann, Knopman et al. 2011).
•Patient has a clearly documented history of cognitive decline over at least 12 months.
•Patient has MRI/CT scan, performed within 12 months before Screening, with findings consistent with the diagnosis of AD without any other clinically significant comorbid pathologies as detailed in Appendix 3. If MRI/CT was not performed within 12 months before Screening, it can be done during the screening period
•MMSE score of 20 26 (inclusive) at Screening and stability of MMSE - no more than three-point change on successive screening and baseline visits before randomization.
•Patient has a CDR GS of 0.5 1 (mild dementia) at Screening.
•Patients taking acetylcholinesterase inhibitors and or memantine for the treatment of AD may be enrolled if the patient has been taking such medication for at least 6 months before Visit 2 (Baseline) and is stable on any dose for the last 4 months prior to Baseline, and if the dose is not expected to change during study participation.
•Patients not receiving acetylcholinesterase inhibitors may be enrolled but must be stable off acetylcholinesterase inhibitors for at least 3 months before Baseline, and agreeable to not starting throughout the first 26 weeks of the trial.
•Patient has a negative drug screen (benzodiazepines or opiates) at Screening. Positive drug screen of BZDs, is allowed only if the use is intermittent and drug intake was 4 days or more before the visit
•Female patients must have had last natural menstruation ≥ 24 months before Screening OR be surgically sterile.
•Male patients and their female spouse/partners who are of childbearing potential must agree to use highly effective methods of contraception, consisting of 2 forms of birth control (at least one of which must be a barrier method) starting at Screening, throughout the study and for 90 days post last dose, OR be surgically sterile.
•Patients who are taking medications for non excluded concurrent medical conditions should be on a stable dose for at least 4 weeks before Screening. Patients taking allowed antidepressants (see Section 12.9) should be on a stable dose for at least 3 months before Screening and throughout the study
•Patient has ability and commitment to spend at least 2 hours per day exposed to daylight (preferably outside but can be next to a window if weather or personal situation does not permit).
•Participant and study partner have the ability to read and write in English or Spanish and have hearing, vision, and physical abilities adequate to perform assessments (corrective aids allowed).
•Participant and study partner are fully vaccinated for COVID 19 including booster doses as indicated (6 months post second dose). Having been diagnosed with COVID 19 after completing the initial full Covid vaccine would meet the requirements for a booster shot

Exclusion criteria

•Declines whole genome screening for 2:107,510,000-107,540,000 polymorphism and APOE4 genotyping.
•Patient is 2:107,510,000-107,540,000 polymorphism carrier.
•Patient has an alternative cause for dementia other than AD.
•A past or recent CT or MRI scan or report indicating any cortical infarct defined as > 1.5 cm3; more than 2 lacunar infracts defined as ≤ 1.5 cm3; or diffuse white matter disease), Fazekas score of more than 1 on MRI or CT scan (more details Appendix 3).
•Patient has evidence of any clinically significant neurodegenerative disease, or other serious neurological disorders other than AD as detailed in Appendix 3,
•Patient has a concurrent psychiatric disorder that prevents his/her participation in the trial including but not limited to Schizophrenia, Bipolar and related disorders, Substance use disorders within the past 2 years, major depression, etc.
•Patient has a history of uncontrolled or untreated cardiovascular, endocrine, gastrointestinal, respiratory, or rheumatologic disorders within the past 5 years.
•Patient has a history of severe agitation and medically treated agitation.
•Patient has a history of serious infectious disease including:
-Neurosyphilis
-Meningitis
-Encephalitis
•Patient has a history of a primary or recurrent malignant disease that has not been in remission for > 5 years prior to the Screening visit, with the exceptions of excised cutaneous squamous cell carcinoma in situ, basal cell carcinoma without recurrences; and history of intraductal breast cancer, cervical carcinoma in situ, or in situ prostate cancer resected over 5 years previously. (For resected in situ prostate cancer, i.e., high grade intraepithelial neoplasia, the patient must have a normal prostate specific antigen [PSA] prior to Screening and no increase in PSA since his resection surgery).
•Patient has severe pain that is likely to interfere with sleep (in the opinion of the investigator).
•Patient has any concomitant documented progressive disease likely to interfere with the conduct of the study, particularly:
-Liver disease with aspartate aminotransferase (AST), alanine aminotransferase (ALT) or gamma glutamyltransferase (GGT) > 3 times the upper limits of normal (ULN)
-Total bilirubin > 3 times the ULN
-Mean corpuscular volume > 95 µ3 if due to chronic alcoholism
-Renal failure with creatinine < 30 ml / min
•Patients that are taking prohibited medications according to Appendix 2 See also section 12.9.
•Continuous use of benzodiazepines or other sedative hypnotics during the 2 weeks before Screening (see Section 12.9).
•Patient has a history of chronic use (more than 3 months of continuous use) and abuse of benzodiazepines or other sedative hypnotics.
•Use of any kind of melatonin/melatonin agonist during the 2 weeks before Screening (see Section 12.9).
•Patient has known or suspected hypersensitivity to exogenous melatonin or melatonin receptor agonists.
•Patient has clinically significant abnormal laboratory findings that have not been approved by the study safety officer.
•Patient has persistent bradycardia (heart beat < 50 bpm) or tachycardia (heart beat > 100 bpm).
•Patient has atrioventricular block (type II/Mobitz II and type III), congenital long QT syndrome, sinus node dysfunction or a marked prolongation of QTc interval (repeated demonstration in ECGs of QTc interval > 450 msec for males and > 470 msec for females using Fridericia's formula: QTc = QT/cube root of RR).
•Patient has other serious diseases that could interfere with patient assessment, in the opinion of the investigator.
•Patient has untreated B12 and/or folic acid deficiency.
•Patient has participated in a clinical trial with any investigational agent within 3 months before Screening. Participants in any former monoclonal antibody clinical trial for AD are not eligible until 6 months after the last visit of the previous study. Patients who have received active vaccine for AD in the past will be excluded.
•Patient with a body mass index (BMI) above 35 or below 18.
•Lifestyle exclusions:
•Patients unwilling to limit alcohol intake to less than 30 g of pure alcohol per day (see Appendix 1) and to abstain after 2000h throughout the study
•Patients unwilling to be exposed to at least 2 hours of daylight each day
•Divergence from the accepted level of study medication compliance (70% 130% of expected consumption) as verified at Visit 2 (see Section 12.10)
•Patients consuming more than 7 cups of tea or coffee (or equivalent amount of caffeine [650 mg] in other caffeinated beverages) per day
•Patients with an irregular lifestyle or life pattern (e.g., shift workers, patients likely to be jet lagged)
•Patients with evidence of serious risk of suicide based on the Columbia-Suicide Severity Rating Scale, i.e., active suicidal ideation with some intent to act, with or without a specific plan (a positive response to Suicidal Ideation Items 4 or 5) in the 6 months prior to Screening, OR with evidence of suicidal behavior in the 2 years prior to Screening (a positive response to any of the 5 Suicidal Behavior Items {actual attempt, interrupted attempt, aborted attempt, preparatory acts, or behavior}), OR who, in the opinion of the investigator, present a serious risk of suicide.

Endpoints (5)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Coverage by outcome category

Global cognition
2
Function / daily living
1
Safety / tolerability / PK
1
Other clinical outcomes
1

Global cognition

2 endpoints
Primary/protocol endpoint

Alzheimer's Disease Assessment Scale cognitive subscale (ADAS-cog 14)

Time frame:26 weeks

ADAS-Cog

change from baseline, improvement

Secondary/protocol endpoint

Mini-Mental State Examination (MMSE)

Time frame:26 weeks

Mini-Mental State Examination (MMSE)

change from baseline, improvement

Function / daily living

1 endpoint
Secondary/protocol endpoint

Alzheimer's Disease Cooperative Study - instrumental Activities of Daily Living (ADCS-iADL)

Time frame:26 weeks

ADCS-Activities of Daily Living (ADCS-ADL)

descriptive

Safety / tolerability / PK

1 endpoint
Secondary/protocol endpoint

Clinical Safety - descriptive statistics for Adverse Events

Time frame:26 weeks, 78 weeks

event count, event

Other clinical outcomes

1 endpoint
Secondary/protocol endpoint

ADCS-Clinical Global Impression of Change (CGIC)

Time frame:26 weeks

change from baseline, improvement

Publications (1)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Registry references + supporting bibliography

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 21, 2026
Endpoint classificationDelfa ADRD endpoint taxonomy
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 21, 2026 snapshot.