Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 65/100

Failure Rate

17.4%

4 terminated/withdrawn out of 23 trials

Success Rate

81.8%

-4.7% vs industry average

Late-Stage Pipeline

4%

1 trials in Phase 3/4

Results Transparency

50%

9 of 18 completed trials have results

Key Signals

9 with results

Enrollment Performance

Analytics

N/A
13(72.2%)
Phase 1
4(22.2%)
Phase 4
1(5.6%)
18Total
N/A(13)
Phase 1(4)
Phase 4(1)

Activity Timeline

Global Presence

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Clinical Trials (23)

Showing 20 of 23 trials
NCT02497950Completed

HeartMate 3 ELEVATE™ Registry

Role: collaborator

NCT01571037Phase 1Completed

Inhaled Milrinone Use in Patients Receiving HeartMate II LVAD: A Pilot Study

Role: collaborator

NCT02279979Not ApplicableTerminated

Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial

Role: collaborator

NCT00121472Not ApplicableCompleted

Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Bridge to Cardiac Transplantation

Role: collaborator

NCT02170363Not ApplicableCompleted

HeartMate 3™ CE Mark Clinical Investigation Plan

Role: collaborator

NCT00121485Not ApplicableCompleted

Thoratec HeartMate II Left Ventricular Assist System (LVAS) for Destination Therapy

Role: collaborator

NCT02224755Not ApplicableCompleted

MOMENTUM 3 IDE Clinical Study Protocol

Role: collaborator

NCT01568424Not ApplicableCompleted

CentriMag RVAS U.S. Post-approval Study Protocol

Role: collaborator

NCT00819793Not ApplicableCompleted

CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulmonary Bypass

Role: collaborator

NCT01452802Completed

Risk Assessment and Comparative Effectiveness of Left Ventricular Assist Device (LVAD) and Medical Management

Role: collaborator

NCT02475460Not ApplicableCompleted

HeartMate 3™ LIS Study

Role: collaborator

NCT01171950Not ApplicableWithdrawn

CentriMag Ventricular Assist System in Treating Failure-to-Wean From Cardiopulmonary Bypass for Pediatric Patients

Role: collaborator

NCT01485666Completed

Thoratec's Reduce Driveline Trauma Through Stabilization and Exit Site Management Study

Role: collaborator

NCT02158403Not ApplicableCompleted

PREVENtion of HeartMate II Pump Thrombosis

Role: collaborator

NCT01577433Completed

Driveline Silicone Skin Interface Registry

Role: collaborator

NCT00983190Not ApplicableCompleted

BeneMACS Study:HeartMate 2 (HM2)Left Ventricular Assist Device (LVAD) Survival in Non Transplant Patients is Equal/Better Than Results in Medical Literature

Role: collaborator

NCT02156583Completed

Frailty: Prevalence and Response to Left Ventricular Assist Device Therapy in Older Heart Failure Patients

Role: collaborator

NCT02460770Phase 1Withdrawn

Bone Marrow-derived Mesenchymal Stem Cells (MSC) Administration in Weaning From Left Ventricular Assist Device

Role: collaborator

NCT00585546Phase 1Terminated

Harefield Recovery Protocol Study for Patients With Refractory Chronic Heart Failure

Role: collaborator

NCT01977703Not ApplicableCompleted

Prospective Randomized Evaluation of an Ultra Conservative Approach to Implantable Defibrillator (ICD) Programming in Patients With a Left Ventricular Assist Device (LVAD).

Role: collaborator