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.
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).
Show all 13Show fewer
- 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
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.
- Conditions
- Acute Ischemic Stroke
- 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 group | Role | What they receive |
|---|---|---|
| PCSK9 inhibitors combined with atorvastatin/rosuvastatin | Experimental | Not described Receives: Drug: PCSK9 inhibitors combined with atorvastatin/rosuvastatin |
| Atorvastatin/rosuvastatin | Sham comparator | Not described Receives: Drug: Atorvastatin/Rosuvastatin |
What is being measured
The primary outcome is the main question the study is designed to answer.
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
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)
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
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
The change in NIHSS score from baseline to 1 day post-randomization.
Measured: One day after randomization
The change in NIHSS score from baseline to 3 day post-randomization.
Measured: 3 day after randomization
The change in NIHSS score from baseline to 7 day post-randomization.
Measured: 7 days after randomization
mRS score at 90 days post-randomization
Measured: 90 days after randomization
Proportion of patients with mRS score of 0-1 at 90 days post-randomization
Measured: 90 days after randomization
Proportion of patients with mRS score of 0-2 at 90 days post-randomization
Measured: 90 days after randomization
Proportion of patients with mRS score of 0-3 at 90 days post-randomization
Measured: 90 days after randomization
Stroke recurrence rate within 30 days post-randomization
Measured: Within 30 days of randomization
Stroke recurrence rate within 90 days post-randomization
Measured: Within 90 days of randomization
The change in lipid parameters from baseline to 7 days post-randomization or at discharge
Measured: 7 days after randomization
The proportion of systemic bleeding within 3 days post-randomization (according to the GUSTO criteria)
Measured: Within 3 days of randomization
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
The incidence of any adverse events or serious adverse events within 90 days post-randomization
Measured: Within 90 days of randomization
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.
- First posted20 Nov 2024
- Study start29 Nov 2024
- Primary completion1 Mar 2026
- Study completion3 Jun 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Acute Ischemic StrokeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Xiang Luo
- Sponsor type
- University, hospital or other
- Collaborators
- The Third People's Hospital of Hubei Province, Yichang Central People's Hospital, The Fifth Hospital of Wuhan, Shanghai Zhongshan Hospital, Renmin Hospital of Wuhan University, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan Third Hospital, Taihe Hospital, Tianyou Hospital Affiliated to Wuhan University of Science and Technology, Santai People's Hospital, The General Hospital of Central Theater Command, Minda Hospital of Hubei Minzu University, Hubei Shiyan People's Hospital, Zigong Fourth People's Hospital, Wuhan No.1 Hospital, Hanyang Hospital Affiliated to Wuhan University of Science and Technology, Changjiang Shipping General Hospital, Wuhan NO. 4 hospital, Affiliated Renhe Hospital of China Three Gorges University, China, Wuhan Central Hospital, Nanyang Central Hospital, Yichang Yiling Hospital, Mianyang Central Hospital, Xihua First Hospital, Neijiang No.2 People's Hospital, The Central Hospital of Huanggang, The Tirst People's Hospital of Mianyang, People's Hospital of Dangyang, Chengdu Jingdongfang Hospital, Wuhan Hankou Hospital, Zhongxiang Traditional Chinese Medicine (TCM) Hospital, Sichuan Science City Hospital, The People's Hospital of Huangpi, Ba Zhong Shi Zhong Yi Yi Yuan, Beichuan Qiang Autonomous County People's Hospital, The First People's Hospital of Mianyang
- Responsible party
- Sponsor-investigator, Xiang Luo, Tongji Hospital
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
Study at a glance
From the registry record, last updated by the sponsor on 9 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Efficacy and Safety of Early Combined Therapy With PCSK9 Inhibitors and Statins in Acute Ischemic Stroke (CAPTAIN)--A Multicenter, Prospective, Randomized Trial
- ClinicalTrials.gov ID
- NCT06696820
- Acronym / sponsor ID
- CAPTAIN / 1100939
- Conditions
- Acute Ischemic Stroke
- Keywords
- Acute Ischemic Stroke, PCSK9 inhibitor
- Phase
- Phase 2/3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 429 participants (actual)
- Lead sponsor
- Xiang LuoUniversity, hospital or other
- Collaborators
- The Third People's Hospital of Hubei Province, Yichang Central People's Hospital, The Fifth Hospital of Wuhan, Shanghai Zhongshan Hospital, Renmin Hospital of Wuhan University, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan Third Hospital, Taihe Hospital, Tianyou Hospital Affiliated to Wuhan University of Science and Technology, Santai People's Hospital, The General Hospital of Central Theater Command, Minda Hospital of Hubei Minzu University, Hubei Shiyan People's Hospital, Zigong Fourth People's Hospital, Wuhan No.1 Hospital, Hanyang Hospital Affiliated to Wuhan University of Science and Technology, Changjiang Shipping General Hospital, Wuhan NO. 4 hospital, Affiliated Renhe Hospital of China Three Gorges University, China, Wuhan Central Hospital, Nanyang Central Hospital, Yichang Yiling Hospital, Mianyang Central Hospital, Xihua First Hospital, Neijiang No.2 People's Hospital, The Central Hospital of Huanggang, The Tirst People's Hospital of Mianyang, People's Hospital of Dangyang, Chengdu Jingdongfang Hospital, Wuhan Hankou Hospital, Zhongxiang Traditional Chinese Medicine (TCM) Hospital, Sichuan Science City Hospital, The People's Hospital of Huangpi, Ba Zhong Shi Zhong Yi Yi Yuan, Beichuan Qiang Autonomous County People's Hospital, The First People's Hospital of Mianyang
- Study start
- 29 Nov 2024 (actual)
- Primary completion
- 1 Mar 2026 (actual)
- Study completion
- 3 Jun 2026 (actual)
- First posted
- 20 Nov 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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:
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| PCSK9 inhibitors combined with atorvastatin/rosuvastatin | Experimental | Drug: PCSK9 inhibitors combined with atorvastatin/rosuvastatin |
| Atorvastatin/rosuvastatin | Sham comparator | Drug: Atorvastatin/Rosuvastatin |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (7 listed)
- 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.
Key exclusion criteria (13 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PCSK9 inhibitors combined with atorvastatin/rosuvastatinA single subcutaneous injection of 420 mg Evolocumab upon admission, along with a standard dose of 20 mg Atorvastatin or 10 mg Rosuvastatin | Drug | PCSK9 inhibitors combined with atorvastatin/rosuvastatin |
| Atorvastatin/RosuvastatinConventional Atorvastatin 20 mg / Rosuvastatin 10 mg | Drug | Atorvastatin/rosuvastatin |
Primary outcome
Proportion of early neurological deterioration
Time frame: Within 3 days of randomization
The proportion of patients with an increase of ≥2 points in the NIHSS score from baseline within 3 days post-randomization
The proportion of moderate-to-severe systemic bleeding within 3 days post-randomization (according to the GUSTO criteria)
Time frame: Within 3 days of randomization
16 secondary outcomes
The proportion of patients with an increase of ≥4 points in the NIHSS score from baseline within 3 days post-randomization
Time frame: Within 3 days of randomization
Proportion of early neurological improvement
Time frame: Within 3 days of randomization
The change in NIHSS score from baseline to 1 day post-randomization.
Time frame: One day after randomization
The change in NIHSS score from baseline to 3 day post-randomization.
Time frame: 3 day after randomization
The change in NIHSS score from baseline to 7 day post-randomization.
Time frame: 7 days after randomization
mRS score at 90 days post-randomization
Time frame: 90 days after randomization
Proportion of patients with mRS score of 0-1 at 90 days post-randomization
Time frame: 90 days after randomization
Proportion of patients with mRS score of 0-2 at 90 days post-randomization
Time frame: 90 days after randomization
Proportion of patients with mRS score of 0-3 at 90 days post-randomization
Time frame: 90 days after randomization
Stroke recurrence rate within 30 days post-randomization
Time frame: Within 30 days of randomization
Stroke recurrence rate within 90 days post-randomization
Time frame: Within 90 days of randomization
The change in lipid parameters from baseline to 7 days post-randomization or at discharge
Time frame: 7 days after randomization
The proportion of systemic bleeding within 3 days post-randomization (according to the GUSTO criteria)
Time frame: Within 3 days of randomization
The proportion of any type of intracranial hemorrhage within 3 days post-randomization (according to the ECASS III criteria)
Time frame: Within 3 days of randomization
The incidence of any adverse events or serious adverse events within 90 days post-randomization
Time frame: Within 90 days of randomization
All-cause mortality rate within 90 days post-randomization
Time frame: Within 90 days of randomization
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 9 Jun 2026.
- Results publication: PubMed 35143758Gutierrez 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.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
2 sites in 1 country: see every site and its status.
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.