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Clinical trial intelligence report
The SARTAN-AD Trial: A Randomized, Open Label, Proof of Concept Study of Telmisartan vs. Perindopril in Mild-Moderate Alzheimer's Disease Patients
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT02085265-Jul 28, 2026
NCT ID
NCT02085265
Status
TERMINATED
Phase
Phase 2
Sponsor
Sunnybrook Health Sciences Centre
Executive brief
Investment-Ready Snapshot
The SARTAN-AD trial, sponsored by Sunnybrook Health Sciences Centre, aimed to explore the potential of repurposing Telmisartan, an angiotensin receptor blocker (ARB), as a neuroprotective agent in mild to moderate Alzheimer's Disease (AD) patients. The study's termination due to recruitment challenges highlights the difficulties in enrolling participants for Alzheimer's trials, a common issue in this therapeutic area. Should the proof of concept yield positive results, it could pave the way for larger studies, potentially altering treatment paradigms for AD and expanding market opportunities for Telmisartan and Perindopril in this indication. The competitive landscape includes established AD therapies and emerging candidates, necessitating a thorough assessment of clinical efficacy and safety profiles to ensure differentiation.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02085265
Indication
Alzheimer's Disease
Modality
small molecule
Target
Angiotensin II receptor (AT1 receptor) modulation via Telmisartan and Angiotensin-converting enzyme inhibition via Perindopril.
Intervention
Perindopril, Telmisartan
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.