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Acute Ischemic StrokePhase 2/3CAPTAINNCT06696820

Efficacy and Safety of Early Combined Therapy With PCSK9 Inhibitors and Statins in Acute Ischemic Stroke

A Phase 2/3 study testing PCSK9 inhibitors combined with atorvastatin/rosuvastatin and Atorvastatin/Rosuvastatin in people with Acute Ischemic Stroke, run by Xiang Luo at 2 sites in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study is an investigator-initiated, multicenter, prospective, open-label, endpoint-blinded, randomized controlled trial (PROBE design) that includes patients with moderate or severe symptomatic intracranial large vessel atherosclerotic stenosis (sICAS) who present with acute ischemic stroke within 48 hours of… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Acute Ischemic Stroke
What is being tested?
PCSK9 inhibitors combined with atorvastatin/rosuvastatin and Atorvastatin/Rosuvastatin
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
429 participants
Where
2 sitesChina
Study dates
29 Nov 2024to 3 Jun 2026
Phase
Phase 2/3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥ 18 years.
  • Acute ischemic stroke diagnosed by CT or MRI of the head.
  • Symptom onset to randomization within 48 hours, including wake-up strokes or strokes without a witnessed onset. The time of symptom onset is defined as the "last known normal time."
  • NIHSS score ≤ 20.
  • mRS score of 0-1 prior to the current stroke.
  • Moderate or severe intracranial stenosis or occlusion (≥50%) confirmed by CTA, MRA, or DSA, involving the responsible intracranial arteries: intradural internal carotid artery, M1-2 segments of the middle cerebral artery, A1 segment of the anterior cerebral artery, V4 segment of the vertebral artery, basilar artery, or P1 segment of the posterior cerebral artery.
  • The participant or legal representative has signed the informed consent form.

Who cannot join

  • Cardiogenic embolism (e.g., atrial fibrillation, cardiac valvular disease, etc.).
  • Symptomatic intracranial stenosis or occlusion due to arteritis, arterial dissection, moyamoya disease, or other similar conditions.
  • Patients who have received intravenous thrombolysis or mechanical thrombectomy.
  • Use of PCSK9 inhibitors within the 1 month prior to the onset of the stroke.
  • Allergy to statins or PCSK9 inhibitors.
  • Active liver disease, including unexplained persistent elevations of alanine aminotransferase (ALT) and/or aspartate aminotransferase (AST).
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  • Known severe renal impairment (creatinine clearance <30 mL/min).
  • Myopathy.
  • Concurrent use of cyclosporine.
  • Known pregnancy or breastfeeding, or a positive pregnancy test prior to randomization.
  • Life expectancy <3 months (e.g., due to severe cardiopulmonary disease, renal failure, malignancy, or other terminal conditions).
  • Participation in other interventional clinical trials that may impact outcome assessments.
  • Any other condition that, in the investigator's judgment, makes the patient unsuitable for participation or poses significant risks to the patient.

Trial locations and contacts

2 sites in 1 country.

China2 sites
  • Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology

    Wuhan, Hubei, 430030

  • Tongji Hospital,Tongji Medical College, Huazhong University of Science and Technology

    Wuhan, Hubei, 430030

Other trials in China

About this study

Official title: Efficacy and Safety of Early Combined Therapy With PCSK9 Inhibitors and Statins in Acute Ischemic Stroke (CAPTAIN)--A Multicenter, Prospective, Randomized Trial

This study is an investigator-initiated, multicenter, prospective, open-label, endpoint-blinded, randomized controlled trial (PROBE design) that includes patients with moderate or severe symptomatic intracranial large vessel atherosclerotic stenosis (sICAS) who present with acute ischemic stroke within 48 hours of symptom onset.

Patients will be centrally randomized in a 1:1 ratio into two groups:

Read more

Experimental Group: A single subcutaneous injection of 420 mg evolocumab upon admission, combined with standard doses of atorvastatin 20 mg or rosuvastatin 10 mg, along with other standard guideline-based medical treatments.

Control Group: Standard doses of atorvastatin 20 mg or rosuvastatin 10 mg, with the remainder of treatment based on current guidelines.

The primary objective of the study is to evaluate whether early combination therapy with a PCSK9 inhibitor and statins within 48 hours of symptom onset can reduce the incidence of early neurological deterioration in patients with symptomatic intracranial atherosclerotic stenosis (sICAS). The secondary objectives include comparing the effects of early PCSK9 inhibitor and statin combination therapy versus statin monotherapy on the 90-day neurological outcomes of AIS patients, improving early neurological recovery, and reducing the recurrence rate of stroke at 30 and 90 days. The safety objective is to assess whether the combination of early PCSK9 inhibitors and statins, compared to statin monotherapy, increases the incidence of moderate-to-severe systemic bleeding within 3 days post-randomization (based on the GUSTO scale), any type of intracranial hemorrhage (according to the ECASS III criteria), and all-cause mortality within 90 days.

Read the detailed description

Acute ischemic stroke (AIS) is a cerebrovascular disease with high incidence, recurrence, and disability rates, posing a serious threat to human health. Symptomatic intracranial atherosclerotic stenosis (ICAS) is one of the most common causes of ischemic stroke globally. In Asian populations, ICAS is the predominant subtype, accounting for approximately 50% of all ischemic strokes. Despite aggressive and standardized medical therapy, patients with ICAS still face a high recurrence rate of stroke and incidence of early neurological deterioration (END). Over 50% of cases of END occur within 72 hours of AIS onset and are defined as an increase in the NIHSS score by ≥2 or 4 points from baseline, which is closely linked to clinical outcomes. Two previous randomized controlled trials (RCTs) found that combined clopidogrel and aspirin dual antiplatelet therapy can prevent END and improve neurological outcomes in AIS patients. However, the occurrence of END remains high, as drug resistance and swallowing difficulties may hinder timely administration.

Multiple RCTs have shown that statin therapy can reduce the risk of recurrent stroke and improve neurological outcomes, and it is consistently recommended by both domestic and international ischemic stroke guidelines. The SPARCL study, published in the New England Journal of Medicine, demonstrated that in patients with a history of recent stroke, lowering LDL-C from ≥2.6 mmol/L to <1.8 mmol/L significantly reduces the risk of recurrent stroke and cardiovascular events. More recently, the INSPIRES study, published in JAMA Neurology, indicated that early statin therapy within 3 days of AIS onset significantly reduces adverse neurological outcomes, such as the proportion of patients with a 90-day mRS score of 2-6 (11.4% vs. 9.8%, P<0.05), compared to delayed statin therapy, although no significant difference was observed in recurrent stroke events within 90 days. As stroke guidelines have evolved, the LDL-C target for secondary prevention has been lowered from 2.6 mmol/L to below 1.8 mmol/L. Statins and other lipid-lowering agents work through different mechanisms affecting cholesterol synthesis, absorption, and clearance, and their combined use can produce a synergistic effect. At the 2024 annual meeting of the Chinese Stroke Society, experts proposed a new concept for lipid management in AIS patients, focusing on residual lipid risk and early combination therapy to achieve more rapid, sustained, and stable lipid control.

Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors are a novel class of monoclonal antibody-based lipid-lowering drugs that reduce serum LDL-C levels by inhibiting the binding of PCSK9 to LDL receptors. PCSK9 inhibitors are highly effective in lowering lipid levels with minimal adverse effects and high safety. The main PCSK9 inhibitors approved for clinical use are alirocumab and evolocumab. Recent international guidelines have clearly stated that PCSK9 inhibitors can be used in combination with statins or other lipid-lowering agents or as monotherapy in patients who are statin-intolerant or for whom statins are contraindicated. Due to the complementary mechanisms of action between statins and PCSK9 inhibitors, their combined use has been shown to provide a greater-than-additive lipid-lowering effect. Post-hoc analyses of the FOURIER study, published in Stroke, and the ODYSSEY study, published in Circulation, confirmed that in patients with atherosclerotic cardiovascular disease, combination therapy with statins and PCSK9 inhibitors significantly reduced the risk of ischemic stroke (1.2% vs. 1.5%, P=0.005; 1.2% vs. 1.6%, P=0.01), with no significant difference in the risk of hemorrhagic stroke between the groups.

However, it remains unclear whether the combination of statins and PCSK9 inhibitors improves neurological outcomes in acute ischemic stroke, particularly in patients with ICAS, as high-quality evidence is lacking. A multicenter, prospective cohort study found that for AIS patients with ICAS, early combination therapy with statins and PCSK9 inhibitors within 7 days of onset significantly reduced the risk of early stroke recurrence within 30 days (5.59% vs. 2.16%, P=0.039). A single-center, retrospective cohort study demonstrated that early combination therapy with statins and PCSK9 inhibitors within 24 hours of stroke onset significantly reduced the incidence of early neurological deterioration (increase in NIHSS score ≥2 points) within 72 hours compared to statin monotherapy (31.9% vs. 12.5%, P=0.005). Another single-center, retrospective cohort study found that for AIS patients undergoing thrombectomy, early combination therapy with statins and PCSK9 inhibitors reduced the proportion of patients with an NIHSS score at discharge and an mRS score of ≤3 (35.6% vs. 52.4%, P=0.041) without increasing the risk of symptomatic intracranial hemorrhage (8.7% vs. 2.4%, P=0.16). Although the reduction in early neurological deterioration was not statistically significant (20.1% vs. 11.9%, P=0.21), these studies support the effectiveness and safety of statin and PCSK9 inhibitor combination therapy in improving neurological outcomes in AIS, providing a reliable foundation for further high-quality RCTs.

This multicenter, prospective, randomized controlled study aims to investigate and evaluate the effects of early combination therapy with PCSK9 inhibitors and statins on early neurological deterioration and other neurological outcome measures in patients with symptomatic intracranial atherosclerotic stenosis, which holds significant clinical value.

Being tested
PCSK9 inhibitors combined with atorvastatin/rosuvastatin, Atorvastatin/Rosuvastatin
Keywords
Acute Ischemic Stroke, PCSK9 inhibitor
Medical subject headings
Ischemic Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • PCSK9 inhibitors combined with atorvastatin/rosuvastatinDrug

    A single subcutaneous injection of 420 mg Evolocumab upon admission, along with a standard dose of 20 mg Atorvastatin or 10 mg Rosuvastatin

  • Atorvastatin/RosuvastatinDrug

    Conventional Atorvastatin 20 mg / Rosuvastatin 10 mg

Study groups in NCT06696820
Study groupRoleWhat they receive
PCSK9 inhibitors combined with atorvastatin/rosuvastatinExperimentalNot described
Receives: Drug: PCSK9 inhibitors combined with atorvastatin/rosuvastatin
Atorvastatin/rosuvastatinSham comparatorNot described
Receives: Drug: Atorvastatin/Rosuvastatin

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proportion of early neurological deterioration

    The proportion of patients with an increase of ≥2 points in the NIHSS score from baseline within 3 days post-randomization

    Measured: Within 3 days of randomization

  2. The proportion of moderate-to-severe systemic bleeding within 3 days post-randomization (according to the GUSTO criteria)

    Measured: Within 3 days of randomization

Secondary outcomes (16)
  1. The proportion of patients with an increase of ≥4 points in the NIHSS score from baseline within 3 days post-randomization

    Measured: Within 3 days of randomization

  2. Proportion of early neurological improvement

    The proportion of patients with a reduction of ≥4 points in the NIHSS score from baseline or a score reduced to 0-1 within 3 days post-randomization.

    Measured: Within 3 days of randomization

  3. The change in NIHSS score from baseline to 1 day post-randomization.

    Measured: One day after randomization

  4. The change in NIHSS score from baseline to 3 day post-randomization.

    Measured: 3 day after randomization

  5. The change in NIHSS score from baseline to 7 day post-randomization.

    Measured: 7 days after randomization

  6. mRS score at 90 days post-randomization

    Measured: 90 days after randomization

  7. Proportion of patients with mRS score of 0-1 at 90 days post-randomization

    Measured: 90 days after randomization

  8. Proportion of patients with mRS score of 0-2 at 90 days post-randomization

    Measured: 90 days after randomization

  9. Proportion of patients with mRS score of 0-3 at 90 days post-randomization

    Measured: 90 days after randomization

  10. Stroke recurrence rate within 30 days post-randomization

    Measured: Within 30 days of randomization

  11. Stroke recurrence rate within 90 days post-randomization

    Measured: Within 90 days of randomization

  12. The change in lipid parameters from baseline to 7 days post-randomization or at discharge

    Measured: 7 days after randomization

  13. The proportion of systemic bleeding within 3 days post-randomization (according to the GUSTO criteria)

    Measured: Within 3 days of randomization

  14. The proportion of any type of intracranial hemorrhage within 3 days post-randomization (according to the ECASS III criteria)

    Measured: Within 3 days of randomization

  15. The incidence of any adverse events or serious adverse events within 90 days post-randomization

    Measured: Within 90 days of randomization

  16. All-cause mortality rate within 90 days post-randomization

    Measured: Within 90 days of randomization

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Nov 2024
  2. Study start29 Nov 2024
  3. Primary completion1 Mar 2026
  4. Study completion3 Jun 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2/3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
429 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06696820
Sponsor's protocol ID
1100939
Acronym
CAPTAIN
Status last verified
Jun 2026
First submitted
17 Nov 2024
Last updated
9 Jun 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Gutierrez J, Turan TN, Hoh BL, Chimowitz MI. Intracranial atherosclerotic stenosis: risk factors, diagnosis, and treatment. Lancet Neurol. 2022 Apr;21(4):355-368. doi: 10.1016/S1474-4422(21)00376-8. Epub 2022 Feb 7.

    PubMed 35143758

Questions about this trial

What is this clinical trial studying?

A Phase 2/3 study testing PCSK9 inhibitors combined with atorvastatin/rosuvastatin and Atorvastatin/Rosuvastatin in people with Acute Ischemic Stroke, run by Xiang Luo at 2 sites in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 9 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proportion of early neurological deterioration (time frame: Within 3 days of randomization). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06696820, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jun 2026.

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