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Intracranial Arteriosclerosis

3
Pipeline Programs
3
Companies
2
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
0
0
0
0
3
0
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Neurotech Pharmaceuticals
1 program
1
Experimental Device A, a self-expanding rapamycin target-eluting stentPhase 31 trial
Active Trials
NCT06925971Not Yet Recruiting279Est. Oct 2027
MicroPort
MicroPortChina - Shanghai
1 program
1
Experimental Device A, a self-expanding rapamycin target-eluting stentPhase 3
AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
1 program
1
Ticagrelor + AspirinPhase 31 trial
Active Trials
NCT05047172Active Not Recruiting1,683Est. Jan 2027

Trial Timeline

Clinical trial activity over time

2022
2023
2024
2025
2026
2027
Neurotech PharmaceuticalsExperimental Device A, a self-expanding rapamycin target-eluting stent
AstraZenecaTicagrelor + Aspirin

Clinical Trials (2)

Total enrollment: 1,962 patients across 2 trials

NCT06925971Neurotech PharmaceuticalsExperimental Device A, a self-expanding rapamycin target-eluting stent

A Randomized Trial of the Rapamycin Target Eluting Stent for the Treatment of Symptomatic Cerebral Artery Atherosclerotic Disease(TARGET-DREAM)

Start: Apr 2025Est. completion: Oct 2027279 patients
Phase 3Not Yet Recruiting
NCT05047172AstraZenecaTicagrelor + Aspirin

Comparison of Anti-coagulation and Anti-Platelet Therapies for Intracranial Vascular Atherostenosis

Start: Aug 2022Est. completion: Jan 20271,683 patients
Phase 3Active Not Recruiting

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

3 late-stage (Phase 3) programs, potential near-term approvals
3 companies competing in this space

The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.