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NCT06696131: TNK in ICH

Tenecteplase (TNK) in the Treatment of Intracerebral Hemorrhage (ICH)

Not yet recruiting Phase 1 Last updated 23 April 2025
What this trial tests

Phase 1 trial testing TNK in Intracerebral Hemorrhage in 5 participants. Not yet recruiting.

Timeline
15 September 2025
Primary endpoint
15 January 2027
31 December 2027

Quick facts

Lead sponsorGaurav Gupta, MD
PhasePhase 1
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment5
Start date15 September 2025
Primary completion15 January 2027
Estimated completion31 December 2027

Drugs / interventions tested

Conditions studied

Sponsor

Gaurav Gupta, MD

Who can join

Adults 18 to 80, any sex, with Intracerebral Hemorrhage or Intracranial Hemorrhages. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The overall purpose of this study is to look at the safety and effectiveness of administering Tenecteplase (TNK) into the brain bleed (hematoma) instead of another clot-dissolving drug known as recombinant tissue plasminogen activator (rtPA), which is the current standard practice. Clot dissolving (Fibrinolytic) drugs work to break down blood clots and have been found to improve health outcomes when applied directly into the hematoma within the brain. Patients who take part in this study will undergo the same surgical procedure that would normally be performed to treat them, but with the exception of TNK not rtPA.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of TNK

Trials testing the same drug.

Other recruiting trials for Intracerebral Hemorrhage

Currently open trials in the same condition.

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/NCT06696131.

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