Microvention-Terumo
Microvention-Terumo sponsors 9 registered US clinical trials on ClinicalTrials.gov, 1 of them currently recruiting, and 6 completed. 0 of these trials are in Phase 3-4 (later-stage) and 1 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Arteriovenous Dural Fistula, with 1 trials.
Trial Pipeline
9 total, page 1 of 1
Post Approval Study - Evaluate the Long-Term Safety and Effectiveness of the WEB Device
NCT04839705
MicroVention, Inc. Flow Re-Direction Endoluminal Device X (FRED™ X™) Post-Approval Study
NCT05409989
Ruptured Aneurysms Treated With Hydrogel Coils
NCT03252314
REal-World Analyses of Stroke - Thrombus Occlusion REtrieval
NCT04451525
PHIL in the Treatment of Intracranial dAVF.
NCT03467542
The WEB-IT Clinical Study
NCT02191618
Pivotal Study of the LVIS (Low Profile Visualized Intraluminal Support)
NCT01793792
Pivotal Study of the FRED Stent System in the Treatment of Intracranial Aneurysms
NCT01801007
Feasibility Study of the LVIS™ (Low-profile Visualized Intraluminal Support)Device
NCT01541254
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 2 | 1 |
What the Pipeline for Microvention-Terumo Shows
According to the ClinicalTrials.gov registry, Microvention-Terumo is linked to 9 US clinical trials across every stage of research activity. Of those, 1 studies are currently recruiting, about 11% of the sponsor's indexed portfolio, and 6 are already marked complete, representing roughly 67% of the total.
The phase mix for Microvention-Terumo reports 0 late-stage studies (Phase 3 and Phase 4 combined) and 1 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Microvention-Terumo is Arteriovenous Dural Fistula with 1 linked trial, and 4 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.