InspireMD Engages Hart Clinical Consultants to Conduct Clinical Trial for CGuard Carotid Stent System in the United States
Tel Aviv, Israel – February 24, 2021 – InspireMD, Inc. (NYSE American: NSPR), developer of the CGuard™ Embolic Prevention System (EPS) for the prevention of stroke caused by carotid artery disease, announced today that it has engaged Hart Clinical Consultants (HCC), a leading Contract Research Organization (CRO) to conduct the clinical trial for its CGuard Carotid Stent System in the United States.
Potential gain:100/+250
Reward/Risk:5-12
Timeframe: up to 1 year
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Tel Aviv, Israel – February 24, 2021 – InspireMD, Inc. (NYSE American: NSPR), developer of the CGuard™ Embolic Prevention System (EPS) for the prevention of stroke caused by carotid artery disease, announced today that it has engaged Hart Clinical Consultants (HCC), a leading Contract Research Organization (CRO) to conduct the clinical trial for its CGuard Carotid Stent System in the United States.
Potential gain:100/+250
Reward/Risk:5-12
Timeframe: up to 1 year
I always try to present the charts in a simple comprehensive format to prevent any confusion.
This is just my technical view, neither a fundamental comment,nor a recommendation to trade..!
Please review my track record and calculate the odds for yourself..!
You’re likes and comments encourage me to continue this.
Stay tuned great live stream and quality content videos coming soon..!
Trade active:
With this clinical trial result, better to consider their FDA approval in their hands:
Results
There were 729 patients (73.03 ± 7.84 years; 516 male) enrolled. Of 131 patients (17.96%), 96 presented with a TIA, 23 with a minor stroke, and 12 with a major stroke. Mean carotid stenosis was 80.13% ± 8.51% (median, 80%; range, 50%-99%). An embolic protection device was employed in 727 patients: distal filter in 589 (80.79%) and proximal occlusion in 138 (18.93%). Technical success was achieved in all but two patients (99.86%), whereas procedural success was 100%. At 24 hours from the procedure, one patient died of a hemorrhagic stroke; two minor strokes and six TIAs were also noted. One patient suffered a nonfatal AMI; ECA occlusion was evident in eight patients (1.09%). To June 2019, 529 patients completed 1-month follow-up. Three new neurologic adverse events were recorded (one minor stroke, two TIAs). One patient suffered an AMI in the absence of a fatal event; ECA patency was 97.6%. Data from 253 patients with 1-year follow-up showed no further neurologic events, whereas 7 deaths were reported (2 fatal AMIs, 4 neoplasms, and 1 suicide). ECA patency was 95.65%.
Results
There were 729 patients (73.03 ± 7.84 years; 516 male) enrolled. Of 131 patients (17.96%), 96 presented with a TIA, 23 with a minor stroke, and 12 with a major stroke. Mean carotid stenosis was 80.13% ± 8.51% (median, 80%; range, 50%-99%). An embolic protection device was employed in 727 patients: distal filter in 589 (80.79%) and proximal occlusion in 138 (18.93%). Technical success was achieved in all but two patients (99.86%), whereas procedural success was 100%. At 24 hours from the procedure, one patient died of a hemorrhagic stroke; two minor strokes and six TIAs were also noted. One patient suffered a nonfatal AMI; ECA occlusion was evident in eight patients (1.09%). To June 2019, 529 patients completed 1-month follow-up. Three new neurologic adverse events were recorded (one minor stroke, two TIAs). One patient suffered an AMI in the absence of a fatal event; ECA patency was 97.6%. Data from 253 patients with 1-year follow-up showed no further neurologic events, whereas 7 deaths were reported (2 fatal AMIs, 4 neoplasms, and 1 suicide). ECA patency was 95.65%.
Trade closed: stop reached