W.L.Gore & Associates

53 total trials 11 currently recruiting 25 completed

W.L.Gore & Associates sponsors 53 registered US clinical trials on ClinicalTrials.gov, 11 of them currently recruiting, and 25 completed. 4 of these trials are in Phase 3-4 (later-stage) and 2 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Aortic Aneurysm, Thoracic, with 3 trials.

Trial Pipeline

53 total, page 1 of 2

RECRUITING NA

GORE® TAG® Thoracic Branch Endoprosthesis Zone 0/1 Post-Approval Study

NCT07166133

RECRUITING NA

GORE® Ascending Stent Graft in the Treatment of De Novo Type A Aortic Dissections

NCT06827990

RECRUITING

Long-term Characterization of GORE® TAG® Conformable Thoracic Stent Graft With ACTIVE CONTROL System Performance

NCT06658730

RECRUITING

Real-World Data Collection of the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis When Used in Covered Endovascular Reconstruction of the Aortic Bifurcation (CERAB) to Treat Aortoiliac Occlusive Disease

NCT06872905

RECRUITING NA

Tissue Reinforcement for Breast Reconstruction (TRBR) Pivotal Clinical Study (REDEFINE)

NCT06556654

RECRUITING

Endovascular AAA Intervention Using the GORE® EXCLUDER® Conformable AAA Endoprosthesis or Iliac Branch Endoprosthesis

NCT06218875

RECRUITING NA

The GORE VBX FORWARD Clinical Study: A Comparison of the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis to Bare Metal Stenting for Patients With Complex Iliac Occlusive Disease

NCT05811364

RECRUITING NA

The GORE® VIABAHN® FORTEGRA Venous Stent Iliofemoral Study

NCT05489588

RECRUITING NA

GORE® ENFORM Biomaterial Product Study

NCT04718168

RECRUITING NA

A Study to Evaluate the Safety and Effectiveness of the InnAVasc Arteriovenous Graft for Hemodialysis Access in Patients With End-Stage Renal Disease

NCT04671771

RECRUITING NA

GORE® CARDIOFORM Septal Occluder and Antiplatelet Medical Management for Reduction of Recurrent Stroke in Patients With Patent Foramen Ovale (PFO): the REDUCE Post Approval Study

NCT03821129

ACTIVE NOT RECRUITING NA

GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis Post-Approval Study

NCT06578741

ACTIVE NOT RECRUITING

Assessment of GORE® SYNECOR Biomaterial in Focused Patient Populations and Long-Term Application

NCT05094089

ACTIVE NOT RECRUITING NA

The GORE® VIABAHN® FORTEGRA Venous Stent IVC Study

NCT05409976

ACTIVE NOT RECRUITING NA

Evaluation of the GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis in the Treatment of Thoracoabdominal and Pararenal Aortic Aneurysms

NCT03728985

ACTIVE NOT RECRUITING NA

Evaluation of the GORE PV1 Device in Patients With Pulmonary Valve Dysfunction

NCT03441971

ACTIVE NOT RECRUITING NA

Assessment of the GORE® EXCLUDER® Conformable AAA Endoprosthesis in the Treatment of Abdominal Aortic Aneurysms

NCT02489539

ACTIVE NOT RECRUITING NA

Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 2

NCT02777593

ACTIVE NOT RECRUITING NA

Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 0/1

NCT02777528

ACTIVE NOT RECRUITING

ARISE: Evaluation of the GORE® Ascending Stent Graft in the Treatment of DeBakey Type I/II Aortic Dissection

NCT02380716

ACTIVE NOT RECRUITING

Global Registry for Endovascular Aortic Treatment (GREAT)

NCT01658787

TERMINATED NA

GORE® CARDIOFORM Septal Occluder Migraine Clinical Study

NCT04100135

TERMINATED NA

Evaluating the Safety and Effectiveness of the InnAVasc Graft for Dialysis Access in Patients With Kidney Failure

NCT03645681

COMPLETED NA

Safety and Efficacy Study of Transcatheter Closure of Ostium Secundum ASDs

NCT02985684

COMPLETED NA

GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis in the Treatment of Type IV Thoracoabdominal Aortic Aneurysms

NCT02528500

COMPLETED NA

In-Stent Restenosis Post-Approval Study

NCT02542267

COMPLETED NA

Early Feasibility of the Branched TAG® Device in the Treatment of Aortic Arch Aneurysms

NCT02264977

COMPLETED NA

A Study of the Gore VIABAHN BX for Treatment of Occlusive Disease in the Iliac Arteries.

NCT02080871

TERMINATED NA

Evaluation of Anti-platelet Factor 4/Heparin Antibodies in Hemodialysis Patients

NCT02165761

COMPLETED NA

Feasibility Study for GORE® TAG® Thoracic Branch Endoprosthesis to Treat Proximal Descending Thoracic Aortic Aneurysms

NCT02021812

COMPLETED NA

Evaluation of the GORE® EXCLUDER® Iliac Branch Endoprosthesis

NCT01883999

COMPLETED NA

The Gore SCAFFOLD Clinical Study

NCT01901874

TERMINATED

Evaluation of GORE® VIABAHN® Endoprosthesis for Popliteal Artery Aneurysm

NCT01902888

COMPLETED NA

Safety and Efficacy of the GORE® Septal Occluder to Treat Ostium Secundum Atrial Septal Defects

NCT01711983

COMPLETED NA

Evaluation of the GORE TIGRIS Vascular Stent

NCT01576055

COMPLETED NA

GORE Flow Reversal System and GORE Embolic Filter Extension Study

NCT01343667

COMPLETED

Open Complex Ventral Incisional Hernia Repair Using Biosynthetic Material for Midline Fascial Closure Reinforcement

NCT01325792

TERMINATED NA

Early TIPS for Ascites Study

NCT01236339

COMPLETED NA

Evaluation of the GORE Conformable TAG® for Treatment of Traumatic Transection

NCT00917852

COMPLETED NA

Evaluation of the GORE Conformable TAG® Thoracic Endoprosthesis for Treatment of Acute Complicated Type B Aortic Dissection

NCT00908388

COMPLETED NA

Thoracic Endoprosthesis for Treatment of Aneurysm of the Descending Thoracic Aortic

NCT00874250

COMPLETED NA

GORE® Septal Occluder Device for Patent Foramen Ovale (PFO) Closure in Stroke Patients

NCT00738894

COMPLETED Phase 3

GORE VIABAHN Endoprosthesis Versus Percutaneous Transluminal Angioplasty (PTA) to Revise AV Grafts in Hemodialysis

NCT00737672

TERMINATED NA

Bioabsorbable Staple Line Reinforcement in Colorectal,Coloanal and Ileoanal Anastomoses

NCT00663819

TERMINATED Phase 4

GORE PROPATEN Vascular Graft vs. Disadvantaged Autologous Vein Graft

NCT00617279

COMPLETED NA

GORE VIABAHN Endoprosthesis With Heparin Bioactive Surface in the Treatment of SFA Obstructive Disease (VIPER)

NCT00541307

COMPLETED Phase 2

GORE TAG® Thoracic Endoprosthesis - 45 mm for the Treatment of Aneurysms of the Descending Thoracic Aorta

NCT00608829

COMPLETED NA

Long-term Safety Study of the GORE® HELEX® Septal Occluder

NCT00581308

COMPLETED Phase 3

GORE Embolic Protection With Reverse Flow

NCT00594100

COMPLETED Phase 2

Study of the Large Diameter GORE EXCLUDER® AAA Endoprosthesis in Abdominal Aneurysms

NCT00615069

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What the Pipeline for W.L.Gore & Associates Shows

According to the ClinicalTrials.gov registry, W.L.Gore & Associates is linked to 53 US clinical trials across every stage of research activity. Of those, 11 studies are currently recruiting, about 21% of the sponsor's indexed portfolio, and 25 are already marked complete, representing roughly 47% of the total.

The phase mix for W.L.Gore & Associates reports 4 late-stage studies (Phase 3 and Phase 4 combined) and 2 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for W.L.Gore & Associates is Aortic Aneurysm, Thoracic with 3 linked trials, and 9 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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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.