Disease × agent evidence record

Prazosin for Alzheimer's Disease and Other Dementias: evidence, trials and status

Synthesis-level literature links Prazosin to Alzheimer's Disease and Other Dementias, but no registered trial in this database tests the pair, so the evidence is observational, pooled from other indications, or pre-dates registry practice.

0 registered trials 0 recruiting 2 publications Evidence tier A · Strong Score 27.0
Research Tracker › Pairs › Alzheimer's Disease and Other Dementias › Prazosin
Research map, not treatment advice. This page aggregates registry and literature records. It does not evaluate efficacy, dosing or safety for any individual. Discuss any treatment decision with a qualified clinician.

Summary

Prazosin has reached the approved stage (maximum clinical phase 4) for at least one indication, so its use in Alzheimer's Disease and Other Dementias would be drug repurposing rather than first-in-human development. This does not mean it is approved for Alzheimer's Disease and Other Dementias. No registered clinical trial in this database tests Prazosin specifically in Alzheimer's Disease and Other Dementias. The evidence below comes from published literature only, so any clinical signal has not yet been tested prospectively against this condition in a registered study. The literature layer holds 2 publications for this pair: 1 Cochrane review and 1 clinical trial publication. Publication years run from 2009 to 2022. Because at least one synthesis-level source exists (systematic review, meta-analysis or Cochrane review), this pair has been assessed beyond single studies, although the synthesis may concern a different indication.

The RepurpOS disease-intelligence file for Alzheimer's Disease and Other Dementias ranks 705 candidate therapeutics from Open Targets, ChEMBL, DGIdb and PubMed; only a minority carry direct clinical evidence, and this page covers one of those. Spontaneous remission context recorded for the condition: Progressive and irreversible by definition; MMSE decline 1.07-3.4 points/year untreated; no spontaneous remission.

Evidence table

Evidence tierA · Strong
Evidence score27.0 (trials 0.0, literature 7.0, tier 15, approved bonus 5.0)
Registered trials0 total: 0 recruiting, 0 active / not yet recruiting, 0 completed, 0 other
Linked publications2 (1 Cochrane review, 1 clinical trial publication)
Agent typeDrug (Small molecule)
Development stage (any indication)Approved
Mechanism / classNot recorded
Data sourcesOpen Targets, ChEMBL
Linked via biomarker / targetABCA1
How the evidence score is calculated
  • Each registered trial scores by status (recruiting / active / enrolling 3, completed 2.5, not yet recruiting 2, unknown 1, terminated / withdrawn / suspended 0.5) plus a phase bonus (phase 3-4 +2, phase 2 +1, phase 1 +0.5). The trial component is capped at 30.
  • Each literature item scores by design (Cochrane review 5, meta-analysis 4, systematic review 3, RCT 3, clinical trial publication 2, curated reference 1.5, other PubMed record 1). The literature component is capped at 30.
  • The existing evidence tier adds 15 (A / Strong), 10 (B / Moderate), 5 (C / Preliminary) or 0 (D / Anecdotal).
  • Agents approved for any indication (max clinical phase 4) add 5, because an approved agent has an established safety profile that lowers the barrier to repurposing trials.
  • The score ranks what has been studied, not what works. It does not read effect sizes or directions of effect.

Registered clinical trials

No registered trial links Prazosin to Alzheimer's Disease and Other Dementias in the current OSMF trial extract.

Search ClinicalTrials.gov for newer studies

Published literature

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Mechanism and notes

No mechanism of action is recorded for this pair in the source databases.

OSMF's existing evidence tier for this pair is A (Strong), derived from the strength of the disease association recorded in Open Targets and ChEMBL, in this case via the biomarker or target ABCA1. The tier describes how well the drug-disease link is documented, not how well the drug works.

Frequently asked questions

Is Prazosin approved for Alzheimer's Disease and Other Dementias?

Prazosin has reached the approved stage (maximum clinical phase 4) for at least one indication, so its use in Alzheimer's Disease and Other Dementias would be drug repurposing rather than first-in-human development. This does not mean it is approved for Alzheimer's Disease and Other Dementias. Approval status for the specific indication should always be confirmed with the relevant regulator and prescribing information.

Is Prazosin in clinical trials for Alzheimer's Disease and Other Dementias?

No registered clinical trial in this database tests Prazosin specifically in Alzheimer's Disease and Other Dementias. The evidence below comes from published literature only, so any clinical signal has not yet been tested prospectively against this condition in a registered study.

What does the evidence show for Prazosin in Alzheimer's Disease and Other Dementias?

Synthesis-level literature links Prazosin to Alzheimer's Disease and Other Dementias, but no registered trial in this database tests the pair, so the evidence is observational, pooled from other indications, or pre-dates registry practice. OSMF's existing evidence tier for this pair is A (Strong), derived from the strength of the disease association recorded in Open Targets and ChEMBL, in this case via the biomarker or target ABCA1. The tier describes how well the drug-disease link is documented, not how well the drug works.

Cite this page

Open Source Medicine Foundation. Prazosin for Alzheimer's Disease and Other Dementias: evidence, trials and status. OSMF Research Tracker. Updated 2026-07-05. https://research.opensourcemed.info/pairs/alzheimers-disease-and-other-dementias/prazosin.html

Data: ClinicalTrials.gov, PubMed, Open Targets, ChEMBL, DGIdb and the OSMF therapeutic agent database. Last updated 2026-07-05. Page built 2026-10-07.

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This is a research map, not treatment advice. Evidence tiers and scores summarise what has been studied, not whether a treatment works or is safe for you.