Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

11.3%

9 terminated/withdrawn out of 80 trials

Success Rate

88.0%

+1.5% vs industry average

Late-Stage Pipeline

1%

1 trials in Phase 3/4

Results Transparency

47%

31 of 66 completed trials have results

Key Signals

2 recruiting31 with results7 terminated

Enrollment Performance

Analytics

N/A
40(80.0%)
Phase 1
5(10.0%)
Phase 2
4(8.0%)
Phase 4
1(2.0%)
50Total
N/A(40)
Phase 1(5)
Phase 2(4)
Phase 4(1)

Activity Timeline

Global Presence

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Clinical Trials (80)

Showing 20 of 80 trials
NCT06604026Not ApplicableCompleted

Investigational Study With the BD PosiFlush™ SafeScrub on NADs

Role: lead

NCT07555548Not Yet Recruiting

UK PureWick™ At-Home Pilot Study

Role: lead

NCT06052449Not ApplicableCompleted

Assessing Social Determinants of Health to Increase Cancer Screening

Role: collaborator

NCT04916067Not ApplicableTerminated

Stoma Closure and Reinforcement Trial ll

Role: collaborator

NCT06806709Not ApplicableRecruiting

Reducing Blood Culture Contamination With the Use of a Needle-less Blood Draw Device (The PIVO Trial)

Role: collaborator

NCT05090722Not ApplicableSuspended

A Pilot Study to Evaluate PureWick for Nocturia

Role: collaborator

NCT06632496Completed

BD Prevue(TM) II Peripheral Vascular Access System With Cue(TM) Needle Tracking Technology Clinical Study

Role: lead

NCT06632509Completed

BD SiteRite(TM) 9 Ultrasound System - Clinical Study

Role: lead

NCT05953363Completed

Prospective Clinical Evaluation of BD NRFit™ Devices and Accessories.

Role: lead

NCT07282860Not ApplicableEnrolling By Invitation

An Evaluation of the PureWick™ Male External Catheter Versus an Established Comparator Overnight in the Home Setting for Incontinence in Adult Males

Role: collaborator

NCT06426121Completed

Clinical Validation of BACTEC™ Plus Aerobic/F Culture Vials Compared With Equivalent Product

Role: lead

NCT04788849Completed

Extended VALidation of HUman Papillomavirus Assays and Collection DEvices for HPV Testing on Self-samples

Role: collaborator

NCT06666426Not ApplicableCompleted

This Study Will Collect Clinical and Patient Reported Experience Data From Participants Requiring Urine Output Management Overnight in the Home Setting.

Role: collaborator

NCT05710718Not ApplicableCompleted

PureWick™ France and U.S. At-Home Pilot Study

Role: collaborator

NCT04461678Not ApplicableCompleted

Clinical Trial for Registration of HPV Nucleic Acid Genotyping Assay Kit

Role: lead

NCT06850259Not ApplicableCompleted

This Study Will Collect Clinical and Patient Reported Satisfaction Data From Males Requiring Urine Output Management Overnight in the Home Setting.

Role: collaborator

NCT06822036Not ApplicableRecruiting

EFFICACY of INTRAOPERATIVE ARISTA POLYSACCHARIDE APPLICATION on the POSTOPERATIVE BLOOD LOSS in PATIENTS UNDERGOING RARP for the TREATMENT of PROSTATE CANCER

Role: collaborator

NCT05553418Not ApplicableCompleted

Investigational On-body Injector Clinical Study

Role: lead

NCT05130762Not ApplicableCompleted

A Post-Market Clinical Follow Up Study to Evaluate BD PureHub™ Disinfecting Cap Use on Needle-Free Connectors

Role: lead

NCT05557422Completed

BD OneFlow CLPD Panel (BD OneFlow LST, and B-CLPD T1 to T4 Assays) on the BD FACSLyric System.

Role: lead