Stroke Clinical Trial Landscape

Daily monitoring for ischemic stroke, intracerebral hemorrhage (ICH), and post-stroke recovery trials, spanning tenecteplase vs. alteplase comparisons, ICH evacuation surgery, neuroprotection, secondary prevention, and rehabilitation. The live trial count is on this page. Updated daily from ClinicalTrials.gov.

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The stroke clinical trial landscape in 2026

Stroke remains one of the largest unmet medical needs in neurology. Despite decades of research, IV tPA and mechanical thrombectomy remain the only acute treatments with proven efficacy, and the treatment window for most patients remains narrow. This gap drives substantial ongoing trial activity across neuroprotection, extended reperfusion windows, hemorrhagic stroke management, and functional recovery.

Stroke trials are often large, multi-site, and operationally complex — making competitive landscape monitoring critical for sponsors managing enrollment against comparable studies.

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Acute ischemic stroke: extending treatment windows

The biggest unmet need in ischemic stroke is extending the treatment window for thrombectomy and thrombolysis. Most major stroke centers globally now perform thrombectomy up to 24 hours in selected patients following DAWN and DEFUSE 3, but the optimal patient selection criteria continue to be refined. Current trials focus on:

Neuroprotection: the field's biggest challenge

Neuroprotection remains the holy grail of stroke therapy — hundreds of compounds have failed in clinical trials after showing promise in animal models. Despite this history, new mechanisms continue to enter trials:

Intracerebral hemorrhage (ICH): an undertreated area

Hemorrhagic stroke has fewer proven treatments than ischemic stroke, making it an active area for new trials:

Stroke recovery and neurorehabilitation

Post-stroke recovery represents a large and growing segment of stroke trial activity. The unmet need is enormous — only 25% of stroke survivors recover full independence. Active trial areas include:

Secondary stroke prevention

With 25% of strokes being recurrent, secondary prevention generates ongoing trial activity:

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Key Phase 3 stroke trials (2025–2026)

The 2026 stroke Phase 3 landscape spans four broad areas: acute thrombolysis optimization, hemorrhagic stroke management, secondary prevention, and neurorehabilitation augmentation. Illustrative active programs:

Program / Drug Sponsor Area Key Question
Tenecteplase vs. alteplase Multiple (academic, NINDS, HRC) Acute ischemic stroke Non-inferiority vs. tPA; single bolus vs. infusion
Andexanet alfa (Andexxa) AstraZeneca / Alexion ICH — anticoagulant reversal Factor Xa reversal outcomes in anticoagulation-related ICH (ANNEXA-I)
Minimally invasive ICH evacuation Multiple (ENRICH, INVEST) ICH — surgical Catheter-directed vs. standard care for lobar/basal ganglia ICH
Inclisiran Novartis Secondary prevention siRNA PCSK9 inhibitor; twice-yearly dosing vs. statin in cerebrovascular outcomes
Colchicine (CONVINCE) Academic (University of Edinburgh) Secondary prevention Anti-inflammatory secondary stroke prevention after non-cardioembolic stroke
Vagus nerve stimulation (VNS) MicroTransponder / LivaNova Stroke recovery Paired VNS + rehabilitation for chronic stroke arm weakness (FDA-cleared)

Tenecteplase vs. alteplase: the biggest acute stroke trial question in 2026

The potential replacement of alteplase (tPA) with tenecteplase for acute ischemic stroke thrombolysis represents one of the most commercially and clinically significant Phase 3 questions in stroke. Tenecteplase offers practical advantages: it is given as a single IV bolus in 5–10 seconds versus alteplase's 1-hour infusion. This simplifies drip-and-ship transfers to thrombectomy centers and reduces the risk of tPA extravasation from long infusion lines.

Multiple major trials have reported results or are enrolling in 2026. The AcT trial in Canada showed non-inferiority; NORTEST-2 and other European programs added confirmatory data. Regulatory submissions are at different stages globally, but tenecteplase has effectively replaced alteplase in several healthcare systems as clinical practice moves ahead of formal approval in some markets. For sponsors developing devices or drugs that interact with IV thrombolysis, understanding the tenecteplase transition is critical competitive intelligence.

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FAQ

Frequently asked questions

How many stroke clinical trials are currently active?
As of September 2026, DataLookout's ClinicalTrials.gov-derived dataset shows 2542 active stroke trials, with 1531 actively recruiting. The pipeline spans acute ischemic stroke treatment, intracerebral hemorrhage management, stroke recovery and neurorehabilitation, and secondary prevention programs. 166 of the active trials are in Phase 3.
What are the key Phase 3 stroke trials running in 2026?
Active Phase 3 stroke trials in 2026 include continued tenecteplase vs. alteplase studies refining non-inferiority findings for acute ischemic stroke thrombolysis (tenecteplase received FDA approval for this indication in March 2025), and multiple intracerebral hemorrhage (ICH) minimally invasive evacuation studies building on the 2023 ENRICH trial, which showed a functional-outcome benefit for early minimally invasive removal of spontaneous ICH. Several DOAC (direct oral anticoagulant) optimal-start-time trials are also underway after cardioembolic stroke.
Is tenecteplase replacing alteplase for ischemic stroke treatment?
Yes. Tenecteplase (TNKase, Genentech) received FDA approval for acute ischemic stroke in March 2025, based on the Phase 3 AcT trial, which showed non-inferiority to alteplase (tPA) in a Canadian cohort of more than 1,500 patients. Tenecteplase offers practical advantages: it is given as a single 5 to 10 second intravenous bolus versus alteplase's roughly one-hour infusion, which simplifies drip-and-ship transfers to thrombectomy centers and reduces the risk of tPA extravasation from long infusion lines. With FDA approval secured, ongoing trials are now refining dosing and patient-selection criteria for both thrombectomy-eligible and non-thrombectomy patients.
How do I monitor stroke clinical trial registrations automatically?
DataLookout checks ClinicalTrials.gov every day and records what changed on each stroke trial (status, enrollment, phase, and more), delivered as an email digest. You can filter by stroke subtype (acute ischemic, hemorrhagic, secondary prevention, recovery), phase, sponsor, and trial status. The free plan ($0 forever) includes one sponsor watchlist, one disease watchlist, and one saved search with daily change detection and an email digest. No credit card required.
Live trial data Data as of 2026-09-16, ClinicalTrials.gov

2542 active trials, 1531 recruiting.

Industry sponsors run 169 of these trials. The rest are run by universities, hospitals, government bodies and other non-commercial sponsors. The table below lists the 5 largest of 138.

View the full Stroke pipeline on the dashboard

Notable trials Ranked by recent tracked changes, ClinicalTrials.gov data as of 2026-09-16
TrialStatusLatest tracked changeSeen
Glucagon-like Peptide-1 Receptor Agonists for Endovascular Stroke Thrombectomy NCT07511543Not Yet RecruitingCompletion moved earlier: 2031-12-30 → 2029-01-312026-09-15
Health, Functioning, Work, and Experiences of Social and Health Services of… NCT06575907Enrolling by InvitationCompletion moved earlier: 2027-12-31 → 2026-092026-09-11
Emergency Stroke Unit for Acute Cerebrovascular Events: A Prospective… NCT06728592RecruitingCompletion pushed: 2027-06-30 → 2028-12-312026-09-11
High-definition Transcranial Electrical Stimulation for Upper Extremity… NCT06409143RecruitingCompletion pushed: 2026-11-30 → 2027-11-302026-08-21
Enhancing Attention and Processing Speed Through Home-based Music… NCT07522463Not Yet RecruitingCompletion pushed: 2026-10-31 → 2027-12-312026-08-20

Each trial page shows every change DataLookout has recorded for that trial.

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DataLookout checks ClinicalTrials.gov every day and records what changed on each trial: status, enrollment, phase, primary endpoint, completion dates, sites, sponsor, and the stated reason a trial stopped. Add a sponsor or a disease to your watchlist, or save any search, and the changes arrive in a daily or weekly email digest.

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