NuVasive

28 total trials 27 completed

NuVasive sponsors 28 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 27 completed. 3 of these trials are in Phase 3-4 (later-stage) and 0 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Degenerative Disc Disease, with 4 trials.

Trial Pipeline

28 total, page 1 of 1

ACTIVE NOT RECRUITING

Long-term Assessment of the Safety and Performance of the NuVasive Simplify Disc

NCT05258435

COMPLETED

Retrospective Modulus ALIF Study

NCT05566704

COMPLETED

Post Approval Study Protocol for the Two Level Simplify® Cervical Artificial Disc

NCT04980378

COMPLETED

XLIF Decade Plate System Study

NCT04689880

COMPLETED NA

Post-Approval Study Protocol for the Simplify Cervical Artificial Disc

NCT04630626

COMPLETED

MSK Validation Study

NCT04422288

COMPLETED

Modulus in XLIF Study

NCT04418817

COMPLETED

MLX/XLX ACR Expandable Lumbar Interbody Implants

NCT04420143

COMPLETED NA

Investigation of the Two Level Simplify® Cervical Artificial Disc

NCT03123549

COMPLETED

Comprehensive Spinal Alignment Planning Study

NCT02606695

COMPLETED NA

Investigation of the Simplify® Cervical Artificial Disc

NCT02667067

COMPLETED

Advanced XLIF Monitoring Multicenter Study

NCT02272140

COMPLETED

Advanced XLIF Monitoring Pilot Study

NCT02192112

COMPLETED Phase 3

Post-Approval Clinical Trial of the PCM® Cervical Disc

NCT01905930

COMPLETED

A Prospective Non-concurrent Controlled Evaluation of Open and MAS® PLIF

NCT01640977

COMPLETED

Multimodality Neuromonitoring in XLIF

NCT01499680

COMPLETED

SpineTRACK Registry - Spinal Outcomes Registry

NCT01372592

COMPLETED

An Evaluation of Interlaminar Lumbar Instrumented (ILIF™)

NCT01019057

COMPLETED

XLIF® vs. MAS®TLIF for the Treatment of Symptomatic Lumbar Degenerative Spondylolisthesis With or Without Central Stenosis.

NCT01024699

COMPLETED Phase 3

XL TDR® eXtreme Lateral Total Disc Replacement for the Treatment of Lumbar Degenerative Disc Disease (DDD)

NCT00927238

COMPLETED

Osteocel® Plus in Posterior Lumbar Interbody Fusion (PLIF)

NCT00941980

COMPLETED

Osteocel® Plus in Transforaminal Lumbar Interbody Fusion (TLIF)

NCT00947583

COMPLETED

Osteocel® Plus in Anterior Lumbar Interbody Fusion (ALIF)

NCT00948831

COMPLETED

NeuroVision® Dynamic Screw Test Study

NCT01232517

COMPLETED

Osteocel® Plus in eXtreme Lateral Interbody Fusion (XLIF®)

NCT00948532

COMPLETED

Osteocel® Plus in Anterior Cervical Discectomy and Fusion (ACDF)

NCT00942045

COMPLETED NA

Evaluating The Safety and Effectiveness of The NeoDisc™ Versus ACDF in Subjects With Single-Level Cervical Disc Disease

NCT00478088

COMPLETED Phase 3

PCM Cervical Disc System

NCT00578812

What the Pipeline for NuVasive Shows

According to the ClinicalTrials.gov registry, NuVasive is linked to 28 US clinical trials across every stage of research activity. Of those, 0 studies are currently recruiting, about 0% of the sponsor's indexed portfolio, and 27 are already marked complete, representing roughly 96% of the total.

The phase mix for NuVasive reports 3 late-stage studies (Phase 3 and Phase 4 combined) and 0 earlier-phase studies (Phase 1 and Phase 2).

The top therapeutic focus area indexed for NuVasive is Degenerative Disc Disease with 4 linked trials, and 7 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.