Disease × agent evidence record

Argipressin for Stroke (Ischaemic / Cerebrovascular Disease): evidence, trials and status

Argipressin has 2 completed registered trials for Stroke (Ischaemic / Cerebrovascular Disease) but no linked publication, which usually means results are unpublished, pending, or not yet matched to this record.

2 registered trials 0 recruiting 0 publications Evidence tier A · Strong Score 25.0
Research Tracker › Pairs › Stroke (Ischaemic / Cerebrovascular Disease) › Argipressin
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

Argipressin has reached the approved stage (maximum clinical phase 4) for at least one indication, so its use in Stroke (Ischaemic / Cerebrovascular Disease) would be drug repurposing rather than first-in-human development. This does not mean it is approved for Stroke (Ischaemic / Cerebrovascular Disease). ClinicalTrials.gov lists 2 registered trials linking Argipressin to Stroke (Ischaemic / Cerebrovascular Disease): 2 have completed. None of the registered studies carries a drug-development phase label, which is typical for behavioural, device and supplement protocols. It plans or enrolled 1102 participants. Registration activity spans 2006 to 2009. No published literature item is linked to Argipressin and Stroke (Ischaemic / Cerebrovascular Disease) in the OSMF database yet, so the record rests on registry entries alone. Registry entries describe intent to study, not outcomes.

The RepurpOS disease-intelligence file for Ischemic Stroke ranks 577 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: Spontaneous early neurological improvement in 10-20% within 24 hours of ischaemic stroke without intervention; functional independence at 3 months in only 40-50% without revascularisation; 15% 30-day mortality untreated.

Evidence table

Evidence tierA · Strong
Evidence score25.0 (trials 5.0, literature 0.0, tier 15, approved bonus 5.0)
Registered trials2 total: 0 recruiting, 0 active / not yet recruiting, 2 completed, 0 other
Linked publications0
Agent typeDrug (Small molecule)
Development stage (any indication)Approved
Mechanism / classNot recorded
Data sourcesDGIdb
Linked via biomarker / targetACE
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

NCT IDTitleStatusPhaseEnrolment
NCT00390962The "COSMOS"-Study (Copeptin in Osmoregulation and Stress Assessment)
2006
completedNot applicable469
NCT00878813Copeptin for Risk Stratification in Acute Stroke Patients: the CoRisk Study
2009
completedNot applicable1,102

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Published literature

No publication is linked to this pair yet.

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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 DGIdb, in this case via the biomarker or target ACE. The tier describes how well the drug-disease link is documented, not how well the drug works.

Frequently asked questions

Is Argipressin approved for Stroke (Ischaemic / Cerebrovascular Disease)?

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

Is Argipressin in clinical trials for Stroke (Ischaemic / Cerebrovascular Disease)?

ClinicalTrials.gov lists 2 registered trials linking Argipressin to Stroke (Ischaemic / Cerebrovascular Disease): 2 have completed. None of the registered studies carries a drug-development phase label, which is typical for behavioural, device and supplement protocols. It plans or enrolled 1102 participants. Registration activity spans 2006 to 2009.

What does the evidence show for Argipressin in Stroke (Ischaemic / Cerebrovascular Disease)?

Argipressin has 2 completed registered trials for Stroke (Ischaemic / Cerebrovascular Disease) but no linked publication, which usually means results are unpublished, pending, or not yet matched to this record. OSMF's existing evidence tier for this pair is A (Strong), derived from the strength of the disease association recorded in DGIdb, in this case via the biomarker or target ACE. The tier describes how well the drug-disease link is documented, not how well the drug works.

Cite this page

Open Source Medicine Foundation. Argipressin for Stroke (Ischaemic / Cerebrovascular Disease): evidence, trials and status. OSMF Research Tracker. Updated 2026-07-05. https://research.opensourcemed.info/pairs/ischemic-stroke/argipressin.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.