Success Metrics

Clinical Success Rate
78.3%

Based on 18 completed trials

Completion Rate
78%(18/23)
Active Trials
0(0%)
Results Posted
67%(12 trials)
Terminated
5(15%)

Phase Distribution

Ph phase_1
3
9%
Ph early_phase_1
1
3%
Ph not_applicable
6
18%
Ph phase_2
4
12%
Ph phase_3
8
24%
Ph phase_4
5
15%

Phase Distribution

4

Early Stage

4

Mid Stage

13

Late Stage

Phase Distribution27 total trials
Early Phase 1First-in-human
1(3.7%)
Phase 1Safety & dosage
3(11.1%)
Phase 2Efficacy & side effects
4(14.8%)
Phase 3Large-scale testing
8(29.6%)
Phase 4Post-market surveillance
5(18.5%)
N/ANon-phased studies
6(22.2%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

62.1%

18 of 29 finished

Non-Completion Rate

37.9%

11 ended early

Currently Active

0

trials recruiting

Total Trials

33

all time

Status Distribution
Active(1)
Completed(18)
Terminated(11)
Other(3)

Detailed Status

Completed18
Withdrawn6
Terminated5
unknown3
Not yet recruiting1

Development Timeline

Analytics

Development Status

Total Trials
33
Active
0
Success Rate
78.3%
Most Advanced
Phase 4

Trials by Phase

Early Phase 11 (3.7%)
Phase 13 (11.1%)
Phase 24 (14.8%)
Phase 38 (29.6%)
Phase 45 (18.5%)
N/A6 (22.2%)

Trials by Status

completed1855%
unknown39%
not_yet_recruiting13%
terminated515%
withdrawn618%

Recent Activity

Clinical Trials (33)

Showing 20 of 33 trialsScroll for more
NCT07228663Phase 3

Hip Fracture Surgery Arterial and Venous Thrombotic Events Prevention

Not Yet Recruiting
NCT02744092Not Applicable

Direct Oral Anticoagulants (DOACs) Versus LMWH +/- Warfarin for VTE in Cancer

Completed
NCT01499953Phase 3

Superficial Vein Thrombosis (SVT) Treated With Rivaroxaban Versus Fondaparinux

Completed
NCT00789399Not Applicable

A Study of the Efficacy of Preventive Dosing of Fondaparinux Sodium Versus Placebo for the Prevention of Venous Thromboembolism (VTE) in Patients Undergoing Coronary Bypass Surgery Receiving Routine Mechanical Prophylaxis

Terminated
NCT00493896Phase 3

Safety of Fondaparinux as Routine VTE Prophylaxis in Medical ICU Patients

Terminated
NCT01727401Phase 4

Thromboprophylaxis of Venous Thromboembolism in Acutely-ill Medical Inpatients With Thrombocytopenia

Terminated
NCT04368377Phase 2

Enhanced Platelet Inhibition in Critically Ill Patients With COVID-19

Completed
NCT00673439Phase 2

Fondaparinux for the Treatment of Heparin-Induced Thrombocytopenia (HIT)

Terminated
NCT00603824Phase 4

Fondaparinux in Patients With Acute Heparin-Induced Thrombocytopenia (HIT)

Withdrawn
NCT00894283Early Phase 1

Comparing Enoxaparin to Fondaparinux to Prevent Venous Thromboembolism (VTE) in Bariatric Surgical Patients

Completed
NCT01857583Phase 3

Safety and Pharmacokinetics Study of DU-176b Administered to Patients With Severe Renal Impairment Undergoing Orthopedic Surgery of The Lower Limbs

Completed
NCT00320424Phase 3

Hip Fracture Study of GSK576428 (Fondaparinux Sodium)

Completed
NCT00320398Phase 3

Total Hip Replacement Study Of GSK576428 (Fondaparinux Sodium)

Completed
NCT01304238

Retrospective Registry of Patients With Acute Heparin-induced Thrombocytopenia Type II

Completed
NCT01444612

Comparative Analysis of Injectable Anticoagulants for Thromboprophylaxis Post Cancer-related Surgery

Completed
NCT00378027

Arixtra PE Study- Outpatient Management of Stable Acute Pulmonary Embolism: Once Daily Subcutaneous Fondaparinux

Withdrawn
NCT00139815Phase 3

Michelangelo - Oasis 5

Completed
NCT00346879Phase 1

Study to Determine Effective Dosing of Fondaparinux in Obese Persons

Withdrawn
NCT01467583Phase 4

Fondaparinux in Critically Ill Patients With Renal Failure

Completed
NCT01406301

Fondaparinux EU-RMP (Adherence)

Completed

Drug Details

Intervention Type
DRUG
Total Trials
33