Success Metrics

Clinical Success Rate
100.0%

Based on 10 completed trials

Completion Rate
100%(10/10)
Active Trials
0(0%)
Results Posted
60%(6 trials)

Phase Distribution

Ph phase_2
4
36%
Ph phase_3
3
27%
Ph phase_1
4
36%

Phase Distribution

4

Early Stage

4

Mid Stage

3

Late Stage

Phase Distribution11 total trials
Phase 1Safety & dosage
4(36.4%)
Phase 2Efficacy & side effects
4(36.4%)
Phase 3Large-scale testing
3(27.3%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

90.9%

10 of 11 finished

Non-Completion Rate

9.1%

1 ended early

Currently Active

0

trials recruiting

Total Trials

11

all time

Status Distribution
Completed(10)
Terminated(1)

Detailed Status

Completed10
Withdrawn1

Development Timeline

Analytics

Development Status

Total Trials
11
Active
0
Success Rate
100.0%
Most Advanced
Phase 3

Trials by Phase

Phase 14 (36.4%)
Phase 24 (36.4%)
Phase 33 (27.3%)

Trials by Status

withdrawn19%
completed1091%

Recent Activity

Clinical Trials (11)

Showing 11 of 11 trials
NCT01387230Phase 3

Evaluate the Efficacy and Safety of GSK573719 Delivered Via a Novel Dry Powder Inhaler in Subjects With COPD

Completed
NCT01372410Phase 2

A Randomized, Double Blind, Placebo Controlled, Incomplete Block, Crossover, Dose Ranging Study to Evaluate the Dose Response of GSK573719 Administered Once or Twice Daily Over 7 Days in Patients With Chronic Obstructive Pulmonary Disease (COPD)

Completed
NCT00515502Phase 2

Safety Study Using GSK573719 And Tiotropium In Patients With Chronic Obstructive Pulmonary Disease

Completed
NCT00475436Phase 1

A Single Centre Randomized Study Evaluating The Safety And Tolerability Of GSK573719 In Healthy Volunteers

Completed
NCT00976144Phase 1

Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Effects of GSK573719 (LAMA) and GW642444 (LABA)Administered Individually and Concurrently in Healthy Japanese Subjects

Completed
NCT01128634Phase 1

Pharmacokinetic and Safety of GSK573719 and GW642444 Administered Individually and Concurrently, With Verapamilin in Healthy Subjects

Completed
NCT01521377Phase 1

QTc Study GSK573719+GW642444

Completed
NCT01316913Phase 3

24-week Trial Comparing GSK573719/GW642444 With GSK573719 and With Tiotropium in Chronic Obstructive Pulmonary Disease

Completed
NCT01702363Phase 3

Long-term Safety Study for GSK573719 in Japanese

Completed
NCT00732472Phase 2

A Study to Assess the Safety and Tolerability of Once Daily Inhaled Doses of GSK573719 Made With Magnesium Stearate in Subjects With Chronic Obstructive Pulmonary Disease(COPD)for 7 Days

Completed
NCT01653483Phase 2

Aura Adolescent PK Study GSK2829332

Withdrawn

All 11 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
11