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Chronic Subdural Hematoma

0
Pipeline Programs
3
Companies
3
Clinical Trials
1 recruiting
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
0
0
Early DiscoveryClinical DevelopmentMarket

Competitive Landscape

3 companies ranked by most advanced pipeline stage

Scientia Vascular
Scientia VascularUT - West Valley City
1 program
Matched pair Aristotle 14 guidewire and Plato 17 microcatheterN/A1 trial
Active Trials
NCT07324551Recruiting100Est. Jul 2029
Oregon Therapeutics
Oregon TherapeuticsFrance - Paris
1 program
Middle Meningeal Artery Embolization (MMAE) Outcomes for Chronic Subdural Hematoma (cSDH)N/A
BALT
BALTCA - Irvine
1 program
SQUIDN/A2 trials
Active Trials
NCT07255508Not Yet Recruiting100Est. Nov 2027
NCT04410146Completed310Est. May 2024

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
Scientia VascularMatched pair Aristotle 14 guidewire and Plato 17 microcatheter
BALTSQUID
BALTSQUID

Clinical Trials (3)

Total enrollment: 510 patients across 3 trials

NCT07324551Scientia VascularMatched pair Aristotle 14 guidewire and Plato 17 microcatheter

Microfabricated Microcatheter Advantages in Middle Meningeal Artery Embolization: an Early Experience at a Single Center

Start: Nov 2025Est. completion: Jul 2029100 patients
N/ARecruiting

Efficacy of Prostatic Arteries Embolization Using SQUIDPERI

Start: Nov 2025Est. completion: Nov 2027100 patients
N/ANot Yet Recruiting

The SQUID Trial for the Embolization of the Middle Meningeal Artery for Treatment of Chronic Subdural Hematoma (STEM)

Start: Nov 2020Est. completion: May 2024310 patients
N/ACompleted

Phase Legend

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

Key Insights

1 actively recruiting trials targeting 510 patients
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.