Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 25/100

Failure Rate

8.3%

1 terminated/withdrawn out of 12 trials

Success Rate

91.7%

+5.2% vs industry average

Late-Stage Pipeline

17%

2 trials in Phase 3/4

Results Transparency

55%

6 of 11 completed trials have results

Key Signals

6 with results

Enrollment Performance

Analytics

Phase 2
6(50.0%)
Phase 1
4(33.3%)
Phase 3
2(16.7%)
12Total
Phase 2(6)
Phase 1(4)
Phase 3(2)

Activity Timeline

Global Presence

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Clinical Trials (12)

Showing 12 of 12 trials
NCT06167707Phase 1Completed

Pharmacokinetics and Pharmacodynamics of Subcutaneous vs Intravenous Furosemide in Healthy Volunteers

Role: lead

NCT05528588Phase 2Completed

Furoscix in Heart Failure Patients With Diuretic Resistance

Role: collaborator

NCT04593823Phase 2Completed

Avoiding Treatment in the Hospital With Furoscix for the Management of Congestion in Heart Failure - A Pilot Study

Role: lead

NCT03458325Phase 3Completed

Furoscix Real-World Evaluation for Decreasing Hospital Admissions in Heart Failure

Role: lead

NCT02329834Phase 2Completed

Crossover Study to Compare the Pharmacokinetics and Bioavailability of a Novel Furosemide Regimen Administered Subcutaneously vs. the Same Dose Administered Intravenously in Subjects With Chronic Heart Failure

Role: lead

NCT04161482Phase 1Completed

An Open Label Study to Evaluate the Impact of Duration of Subcutaneous Infusion of a Novel, pH Neutral Formulation of Furosemide (Furoscix®) on Safety and Local Skin Tolerability

Role: lead

NCT02804282Phase 3Completed

Product Design Clinical Performance Study of sc2Wear Furosemide Combination Product

Role: lead

NCT02350725Phase 1Completed

Furosemide Pharmacodynamics and Pharmacokinetics After Subcutaneous or Oral Administration

Role: lead

NCT02579057Phase 2Completed

Sub-Q Versus IV Furosemide in Acute Heart Failure

Role: collaborator

NCT02804035Phase 2Completed

Pilot Study for First Clinical Use of sc2Wear Furosemide Combination Product

Role: lead

NCT02561442Phase 2Completed

Crossover Study to Compare the Pharmacokinetics of Subcutaneous and Intravenous Ceftriaxone Administration

Role: lead

NCT02721511Phase 1Withdrawn

A Study to Investigate the Safety and Efficacy of a Novel Furosemide Regimen

Role: collaborator

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