# Conor Cobalt Chromium Reservoir Based Stent With Sirolimus Elution in Native Coronary Artery Lesions

> **NCT00714883** · PHASE2 · TERMINATED · sponsor: **Cordis US Corp.** · enrollment: 3 (actual)

## Conditions studied

- Coronary Disease

## Interventions

- **DEVICE:** NEVO™ Sirolimus-eluting Coronary Stent System

## Key facts

- **NCT ID:** NCT00714883
- **Lead sponsor:** Cordis US Corp.
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE2
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2008-06
- **Primary completion:** 2009-11
- **Final completion:** 2012-10
- **Target enrollment:** 3 (ACTUAL)
- **Why stopped:** The NEVO™ stent will not be commercialized. Cordis decided to close the study after 3 years. This decision took the absence of safety signals into account.
- **Last updated:** 2012-10-25

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00714883

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00714883, "Conor Cobalt Chromium Reservoir Based Stent With Sirolimus Elution in Native Coronary Artery Lesions". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT00714883. Licensed CC0.

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