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NCT06994975: CHESTNUT

CHinese ischEmic Stroke Beyond 4.5 Hours With TeNecteplase Under Optimized Non-Contrast CT Selection

Recruiting now Phase 3 Last updated 22 December 2025
What this trial tests

Phase 3 trial testing 0.25mg/kg TNK in Acute Ischemic Stroke in 890 participants. Currently enrolling.

Timeline
3 November 2025
Primary endpoint
1 March 2028
1 June 2028

Quick facts

Lead sponsorHuashan Hospital
PhasePhase 3
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment890
Start date3 November 2025
Primary completion1 March 2028
Estimated completion1 June 2028
Sites2 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Huashan Hospital

Who can join

18 and older, any sex, with Acute Ischemic Stroke. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The CHESTNUT trial is a multicenter, open-label, blinded-endpoint, randomized, controlled, phase 3 trial. The primary objective of this study is to explore the efficacy and safety of the dose of 0.25 mg/kg tenecteplase (TNK) in Chinese acute ischemic stroke (AIS) patients without substantial infarction on non-contrast computed tomography (NCCT) in an extended time window.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Acute Ischemic Stroke

Currently open trials in the same condition.

Other Huashan Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06994975.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing