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Compound · clinical trials

Biweekly clinical trials

Also listed in trial records as PCSK9 inhibitor
Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 10 trials in our China and South Korea registers that name Biweekly as an intervention. Synced 28 Sep 2026
10Current trials
7Recruiting now
9Lead sponsors
2Country registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 โ€” Top 14 finalist
Compiled from ClinicalTrials.gov registry records ยท Last verified ยท Editorial standards
At a glance

Biweekly is named as an intervention in 10 current clinical trials in our China and South Korea registers. 7 are recruiting patients now. The most common phase is Not applicable. The sponsor with the most trials is Yun Dai Chen (2). The most-studied condition is Ischemic Stroke.

Trials by status

  • Recruiting770%
  • Not yet open330%

Trials by phase

  • Not applicable440%
  • Observational330%
  • Phase 4220%
  • Phase 2/3110%
01

Clinical trials of Biweekly

10 trials
StudyPhaseStatusLead sponsorRegisters
The Effect of InTensive Statin in Ischemic Stroke With inTracranial Atherosclerotic Plaques
NCT03753555 · ClinicalTrials.gov ↗ · Stroke, Ischemic, Atherosclerosis, Cerebral
Phase 4 Recruiting General Hospital of Shenyang Military Region China
Effect of PCSK9 Inhibitors on Coronary Atherosclerotic Plaques Derived From Optical Coherence Tomography
NCT06520904 · ClinicalTrials.gov ↗ · Coronary Artery Disease, Optical Coherence Tomography
Phase 4 Recruiting First Affiliated Hospital of Xinjiang Medical University China
Study of Predictive Factors Related to Prognosis of Patients With Ischemic Stroke Due to Large-artery Atherosclerosis
NCT04847752 · ClinicalTrials.gov ↗ · Ischemic Stroke, Large-Artery Atherosclerosis (Embolus/Thrombosis)
Observational Recruiting Tongji Hospital China
Multicenter Real-World Cohort Study Evaluating the Impact of Early Intensive Lipid-Lowering Therapy on the Prognosis of Acute Coronary Syndrome Patients(ELITE-ACS)
NCT06738758 · ClinicalTrials.gov ↗ · Acute Coronary Syndromes
Observational Recruiting Yun Dai Chen China
A Cohort Study Comparing PCSK9 Inhibitor Plus Statin With Statin Monotherapy for Carotid Artery Stenosis
NCT07036991 · ClinicalTrials.gov ↗ · Carotid Artery Stenosis
Observational Recruiting Changhai Hospital China
Improving Blood Lipid Management in Symptomatic Intracranial Atherosclerotic Stenosis on Clinical Outcome
NCT05397405 · ClinicalTrials.gov ↗ · Intracranial Artery Stenosis
Not applicable Recruiting Nanjing First Hospital, Nanjing Medical University China
Optimal Target Low-density Lipoprotein Cholesterol Level for Small Vessel Occlusion Stroke
NCT06649240 · ClinicalTrials.gov ↗ · Ischemic Stroke, Small Vessel Cerebrovascular Disease, Cholesterol, LDL
Not applicable Recruiting Seoul National University Hospital South Korea
PCSK9 Inhibitors in Acute Ischemic Stroke Patients Undergoing Endovascular Therapy
NCT07174375 · ClinicalTrials.gov ↗ · Acute Ischemic Stroke
Phase 2/3 Not yet open Nanfang Hospital, Southern Medical University China
Protective Effect of PCSK9 Inhibitor Against Negative Inflammatory Response and Organ Dysfunction After Coronary Artery Bypass Grafting (PANDA VIII)
NCT06730802 · ClinicalTrials.gov ↗ · Myocardial Ischaemic Syndrome, Coronary Heart Disease
Not applicable Not yet open Nanjing Medical University China
Assessing Coronary Non-Culprit Plaque Early with Start of PCSK9 Inhibitors in Acute Myocardial Infarction (ACCESS-AMI)
NCT06854523 · ClinicalTrials.gov ↗ · Acute Myocardial Infarction
Not applicable Not yet open Yun Dai Chen China

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Biweekly

16 conditions
Ischemic Stroke2Intracranial Artery Stenosis1Stroke, Ischemic1Atherosclerosis, Cerebral1Myocardial Ischaemic Syndrome1Coronary Heart Disease1Large-Artery Atherosclerosis (Embolus/Thrombosis)1Coronary Artery Disease1Optical Coherence Tomography1Carotid Artery Stenosis1Acute Myocardial Infarction1Acute Ischemic Stroke1
All 16 conditions
Condition (as registered)Trials
Ischemic Stroke2
Intracranial Artery Stenosis1
Stroke, Ischemic1
Atherosclerosis, Cerebral1
Myocardial Ischaemic Syndrome1
Coronary Heart Disease1
Large-Artery Atherosclerosis (Embolus/Thrombosis)1
Coronary Artery Disease1
Optical Coherence Tomography1
Carotid Artery Stenosis1
Acute Myocardial Infarction1
Acute Ischemic Stroke1
Acute Coronary Syndromes1
Small Vessel Cerebrovascular Disease1
Cholesterol, LDL1
Secondary Prevention1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Yun Dai Chen2
Nanjing First Hospital, Nanjing Medical University1
General Hospital of Shenyang Military Region1
Nanjing Medical University1
Tongji Hospital1
First Affiliated Hospital of Xinjiang Medical University1
Changhai Hospital1
Nanfang Hospital, Southern Medical University1
Seoul National University Hospital1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China96
Clinical trials in South Korea11

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Biweekly trials

How many clinical trials are testing Biweekly?

10 current trials in our China and South Korea registers name Biweekly (also registered as PCSK9 inhibitor) as a drug or biological intervention, as of the registry sync on 28 September 2026. Completed and withdrawn studies are not counted.

Are Biweekly trials recruiting patients?

Yes. 7 of the 10 trials are recruiting: 6 with sites in China and 1 with sites in South Korea. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Biweekly clinical trials?

Yun Dai Chen (2), Nanjing First Hospital, Nanjing Medical University (1), General Hospital of Shenyang Military Region (1) and Nanjing Medical University (1), among 9 lead sponsors in total. The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Biweekly works or whether it is effective, and it is not medical advice.

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How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records โ€” it is not written from memory, and nothing here describes how Biweekly works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Biweekly (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 28 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician โ€” our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us โ€” we correct promptly and log it.