Viewing Study NCT04685590



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Last Modification Date: 2024-10-26 @ 1:52 PM
Study NCT ID: NCT04685590
Status: RECRUITING
Last Update Posted: 2023-12-14
First Post: 2020-12-22

Brief Title: Senolytic Therapy to Modulate the Progression of Alzheimers Disease SToMP-AD Study
Sponsor: Wake Forest University Health Sciences
Organization: Wake Forest University Health Sciences

Study Overview

Official Title: Phase II Clinical Trial to Evaluate the Safety and Feasibility of Senolytic Therapy in Alzheimers Disease
Status: RECRUITING
Status Verified Date: 2023-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SToMP-AD
Brief Summary: The objective of the study is to determine the safety feasibility and efficacy of senolytics in older adults with amnestic mild cognitive impairment MCI or early-stage AD Clinical Dementia Rating CDR05 or 1 who are tau PET positive
Detailed Description: This study is a Phase II multi-site randomized double-blind placebo controlled trial to determine safety feasibility and efficacy of senolytics in older adults with amnestic mild cognitive impairment MCI or early-stage AD Clinical Dementia Rating CDR05 or 1 who are tau PET positive

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: None