Rapamycin - Effects on Alzheimer's and Cognitive Health

NCT04629495 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2025-09-03

No results posted yet for this study

Summary

This study will evaluate the safety, tolerability, and feasibility of 12 month oral rapamycin treatment in older adults with amnestic mild cognitive impairment (aMCI) and early stage Alzheimer's disease (AD).

Conditions

Interventions

DRUG

Rapamycin

RAPA will be administered orally 1mg daily

OTHER

Placebo

Placebo will be administered orally once daily

Sponsors & Collaborators

  • Alzheimer's Association

    collaborator OTHER
  • The University of Texas Health Science Center at San Antonio

    lead OTHER

Principal Investigators

  • Sudha J Seshadri, MD · UT Health San Antonio

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
55 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-11
Primary Completion
2026-03-31
Completion
2026-03-31
FDA Drug
Yes

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04629495 on ClinicalTrials.gov