Key Insights

Highlights

Success Rate

96% trial completion (above average)

Published Results

15 trials with published results (21%)

Research Maturity

54 completed trials (76% of total)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

2.8%

2 terminated out of 71 trials

Success Rate

96.4%

+9.9% vs benchmark

Late-Stage Pipeline

28%

20 trials in Phase 3/4

Results Transparency

28%

15 of 54 completed with results

Key Signals

15 with results96% success

Data Visualizations

Phase Distribution

50Total
Not Applicable (19)
P 1 (4)
P 2 (7)
P 3 (6)
P 4 (14)

Trial Status

Completed54
Unknown9
Recruiting2
Terminated2
Active Not Recruiting1
Withdrawn1

Trial Success Rate

96.4%

Benchmark: 86.5%

Based on 54 completed trials

Clinical Trials (71)

Showing 20 of 20 trials
NCT04475380Completed

Complex All-comers and Patients With Diabetes or Prediabetes, Treated With Xience Sierra Everolimus-eluting Stents

NCT04280029Not ApplicableActive Not RecruitingPrimary

SELUTION SLR™ 014 In-stent Restenosis

NCT05471245Not ApplicableCompletedPrimary

AnGiographic Performance With A Sirolimus-elutiNG Balloon in the TrEatment of De Novo CoronaRy Artery Disease

NCT07239921Not Yet Recruiting

Disease Characteristics of R-CAD

NCT05089864Not ApplicableCompleted

STAR and Deferred Stenting Study

NCT06075602Recruiting

COMPLEX Registry - a Prospective COhort Study to Describe the Management and Outcomes of Patients Presenting with CompLEX and Calcified Coronary Artery Disease

NCT04988685Recruiting

SIROOP Registry - a Prospective Registry Study to Evaluate the Outcomes of Coronary Artery Disease Patients Treated with SIROlimus or Paclitaxel Eluting Balloon Catheters

NCT03074305Not ApplicableWithdrawn

DEB Versus 2nd Generation DES in Patients With In-Scaffold Restenosis of Bioresorbable Vascular Scaffold

NCT01106534Phase 4Completed

XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort

NCT00106587Phase 1CompletedPrimary

Treatment of In-Stent Restenosis by Paclitaxel Coated PTCA Balloons (PACCOCATH - ISR I)

NCT01262703Not ApplicableCompleted

Safety Study of a Bioresorbable Coronary Stent

NCT03667313Phase 3CompletedPrimary

Treatment of In-Stent Restenosis 2 Study

NCT04915391UnknownPrimary

Restenosis in Coronary Stents And Cutaneous HEaLing

NCT01674803Not ApplicableCompleted

Comparison of BIOdegradable Polymer and DuRablE Polymer Drug-eluting Stents in an All COmeRs PopulaTion (BIO-RESORT)

NCT04494750Unknown

Physiology and Residual Ischemia After Percutaneous Coronary Intervention

NCT03242096Not ApplicableCompletedPrimary

Treatment of Coronary In-stent Restenosis (ISR) by a Sirolimus Coated or a Paclitaxel Coated Balloon

NCT00714545Phase 4Completed

SCRIPPS V: Intracoronary Brachytherapy for Recurrent Restenosis After Multiple Drug-Eluting Stents

NCT01894152Completed

XIENCE PRIME Everolimus Eluting Coronary Stent System (EECSS) China Single-Arm Study

NCT01205776Not ApplicableCompleted

EXCEL Clinical Trial

NCT02151812Not ApplicableCompleted

Comparison of Agent™ and SeQuent® Please Paclitaxel Coated Balloon Catheters in Coronary In-stent Restenosis (AGENT-ISR)

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