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PF-08161842

Phase 1

Alzheimer Disease | Small molecule | Neurology |Pfizer, Inc.|Trials Updated: Oct 30, 2026

PF-08161842 development status

Highest phase Phase 1
Registered trials 1 across 1 sponsor since Oct 2026

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindCONTROLLED
Total Trials1
Total Enrollment98

FDA Designations

No designations recorded

PF-08161842 clinical trials

PF-08161842 · 1 trial · 1 indication

Phase 1 1
NCT07897708A Study to Learn How Different Amounts of the Study Medicine Called PF-08161842 Are Tolerated and Act in the Body in Healthy and Older AdultsAlzheimer Disease
NOT YET_RECRUITING98 Analytics
PHASE1NOT YET_RECRUITING
A Study to Learn How Different Amounts of the Study Medicine Called PF-08161842 Are Tolerated and Act in the Body in Healthy and Older Adults
Alzheimer DiseaseUnlock trial analytics

Study Endpoints

Primary Endpoints

Number of Participants With Treatment Emergent Adverse Events (TEAEs)
From first dose through approximately 28 to 35 days after the last dose
Number of Participants With Serious Adverse Events (SAEs)
From first dose through approximately 28 to 35 days after the last dose
Number of Participants With Clinically Significant Laboratory Abnormalities
From first dose through approximately 28 to 35 days after the last dose
Number of Participants With Clinically Significant Vital Signs Abnormalities
From first dose through approximately 28 to 35 days after the last dose
Number of Participants With Clinically Significant Electrocardiogram (ECG) Findings
From first dose through approximately 28 to 35 days after the last dose
Number of Participants With Clinically Significant Columbia-Suicidality Severity Rating Scale (C-SSRS)
From first dose through approximately 28 to 35 days after the last dose

Secondary Endpoints

Area Under the Concentration-time Curve From Time Zero to the Time of the Last Quantifiable Concentration (AUClast)
Part A only: Up to Day 5
Area Under the Curve From Time Zero to end of Dosing Interval (AUCtau)
Part B only: Up to Day 17
Maximum Observed Plasma Concentration (Cmax)
Part A: Up to Day 5 Part B: Up to Day 17
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Study Design & Arms

AllocationRANDOMIZED
MaskingDOUBLE
ModelPARALLEL
PurposeBASIC_SCIENCE

Treatment Arms

ArmTypeDescription
Part A: Cohorts 1-6 and 7 (optional)EXPERIMENTALParticipants will receive PF-08161842 or matching placebo as a single dose on Day 1.
Part B: Cohort 8-12 and 13 (Optional)EXPERIMENTALParticipants will receive doses of PF-08161842 or matching placebo from Day 1 through Day 14.

Interventions

NameTypeDescription
PF-08161842DRUGOral tablet (Parts A and B).
Placebo for PF-08161842DRUGMatching placebo tablet (Parts A and B).
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Eligibility Criteria

Age Range18 Years to 85 Years
SexALL
Healthy VolunteersYes

Inclusion criteria: 1. Healthy adults, ages 18 to 64 years and healthy older adults, ages 65 to 85 years. 2. Body mass index (BMI) of 16-32 kg/m2; and a total body weight \>50kg (110 lb.). Exclusion criteria: 1. Evidence or history of clinically significant medical conditions. 2. Participation in...

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Recent Changes (Last 90 Days)

LOWOct 30, 2026NCT07897708lastUpdatePostDate: changed
LOWOct 30, 2026NCT07897708lastUpdatePostDate: changed
LOWOct 27, 2026NCT07897708NEW_TRIAL: changed
LOWOct 27, 2026NCT07897708NEW_TRIAL: changed