Silk Road Medical Unveils Unprecedented Pivotal Data From The ROADSTER Trial

30 Day Stroke Rate of 1.4% Highlights Excellent Neuroprotection with Novel Hybrid Procedure for Carotid Artery Revascularization

Nov 24, 2014, 15:06 ET from Silk Road Medical, Inc.

SUNNYVALE, Calif., Nov. 24, 2014 /PRNewswire/ -- Silk Road Medical, Inc. announced the 30 day outcomes from the ROADSTER IDE Study were presented this month at the Late Breaking Clinical Trials Session at the 2014 Vascular InterVentional Advances (VIVA) Meeting in Las Vegas, with additional data presented at the VEITH Symposium in New York, NY.  The trial studied the ENROUTE™ Transcarotid Neuroprotection System (NPS) (Silk Road Medical, Inc., Sunnyvale, CA), which is designed to provide direct access to the carotid artery and reduce the risk of stroke during carotid angioplasty and stenting (CAS) by diverting dangerous debris away from the brain with a surgically-inspired mechanism to temporarily reverse blood flow.  The 1.4% 30 day stroke rate was the lowest seen to date of any contemporary prospective trial of CAS. 

Celebrating its 60th anniversary in 2013, carotid endarterectomy (CEA) has been the "Gold Standard" in carotid artery revascularization because of the low stroke and death rates in multiple prospective trials.  Yet CEA is not free of the potential for certain local and systemic complications such as cranial nerve injury and myocardial infarction.

Fifteen years ago transfemoral CAS was introduced with much initial excitement due to the minimally invasive, endovascular advantage, but fell out of favor for physicians and payors due to the excess risk of peri-procedural stroke compared to CEA.  In a standard surgical risk population, the CREST trial demonstrated peri-procedural strokes occur twice as often in transfemoral CAS patients.

ROADSTER was a prospective, multi-center, IDE study designed to evaluate the safety and effectiveness of the ENROUTE Transcarotid NPS in a hybrid procedure combining the best elements of CEA and CAS.  Richard Cambria, MD and Christopher Kwolek, MD of Massachusetts General Hospital served as the trial National Co-Principal Investigators.  Patients were enrolled at 15 vascular surgery sites, one neurosurgery site, and two multi-specialty sites. The primary endpoint was a composite of Any Stroke (S), Death (D), or Myocardial Infarction (MI) through 30 days.

208 (67 lead-in, 141 pivotal) symptomatic and asymptomatic patients who were at high risk for complications from CEA were enrolled.  FDA-approved carotid stent systems were delivered through the direct carotid access point under high rate flow reversal afforded by the ENROUTE Transcarotid NPS.  Baseline pivotal population characteristics included 26% Symptomatic, 35% Female, and 47% Age greater than or equal to 75. 

ROADSTER Trial

Results at 30 days

ITT Population

N=141

Per Protocol Population

N=136

Stroke/Death/MI

3.5%

2.9%

Stroke/Death

2.8%

2.2%

All Stroke

1.4%

0.7%

There were no strokes in patients Age greater than or equal to 75 nor in Symptomatic patients. There was one (0.7%) CNI presenting as hoarseness which fully resolved. 

"These stroke rates in a high surgical risk population are the lowest to date for CAS and comparable to the peri-procedural rates in the standard surgical risk CEA arm of CREST (2.3%).  The Silk Road procedure is less of an operation for the patient than a traditional CEA and can be performed in under an hour with local anesthesia.  With more experience and evidence, vascular specialists can look forward to incorporating this procedure as a true alternative to CEA for patients," commented Dr. Cambria.

Erica Rogers, CEO for Silk Road Medical, commented, "The ROADSTER data support our hypotheses that led to this device design and procedure.  It's all about stroke.  Doctors perform these procedures to reduce the risk of stroke, not to cause a stroke.  The ENROUTE transcarotid platform finally delivers a less invasive alternative with the neuroprotection you would expect from a CEA procedure."

The ENROUTE Transcarotid Platform Regulatory Status
The ENROUTE NPS and Stent Systems are limited by United States law to investigational use; the ENROUTE Transcarotid NPS has been submitted for 510(k) review and the ROADSTER trial also supports the pending Premarket Approval PMA for the ENROUTE Transcarotid Stent System. The ENROUTE Transcarotid NPS and the ENROUTE Transcarotid Stent System have been granted CE Mark.

About Silk Road Medical
Silk Road Medical, Inc. is a private company located in Sunyvale, CA, that develops and manufactures less-invasive medical devices intended to improve the treatment of intra- and extra-cranial cerebrovascular disease through proprietary transcarotid access platforms.  Detailed information about Silk Road Medical can be found at www.silkroadmed.com.

SOURCE Silk Road Medical, Inc.



RELATED LINKS

http://www.silkroadmed.com