Success Metrics

Clinical Success Rate
100.0%

Based on 14 completed trials

Completion Rate
100%(14/14)
Active Trials
0(0%)
Results Posted
36%(5 trials)

Phase Distribution

Ph phase_1
9
64%
Ph phase_3
5
36%

Phase Distribution

9

Early Stage

0

Mid Stage

5

Late Stage

Phase Distribution14 total trials
Phase 1Safety & dosage
9(64.3%)
Phase 3Large-scale testing
5(35.7%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

100.0%

14 of 14 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

0

trials recruiting

Total Trials

14

all time

Status Distribution
Completed(14)

Detailed Status

Completed14

Development Timeline

Analytics

Development Status

Total Trials
14
Active
0
Success Rate
100.0%
Most Advanced
Phase 3

Trials by Phase

Phase 19 (64.3%)
Phase 35 (35.7%)

Trials by Status

completed14100%

Recent Activity

Clinical Trials (14)

Showing 14 of 14 trials
NCT02183441Phase 1

Bioavailability of BI 1356 After Co-administration With Ritonavir Compared to the Bioavailability of BI 1356 Alone in Healthy Male Volunteers

Completed
NCT02173639Phase 1

Bioavailability of Combination Tablet BI 1356/Metformin Compared With Single BI 1356 and Metformin Administered Together to Healthy Male and Female Subjects

Completed
NCT02183402Phase 1

Pharmacokinetics, Safety and Tolerability of Digoxin With or Without Co-administration of BI 1356 in Healthy Volunteers

Completed
NCT02183337Phase 1

Bioavailability of BI 1356 With and Without Co-administration of Pioglitazone and the Bioavailability of Pioglitazone With and Without Coadministration of BI 1356 in Healthy Male and Female Volunteers

Completed
NCT02183428Phase 1

Bioavailability of BI 1356 and Glyburide in Healthy Male and Female Volunteers

Completed
NCT02183376Phase 1

Pharmacokinetics and Pharmacodynamics of BI 1356 in Subjects With Different Degrees of Liver Impairment as Compared to Healthy Subjects

Completed
NCT02175394Phase 1

Effect of Multiple BI 1356 Doses of on the Multiple-dose Pharmacokinetics of a Combination of Ethinylestradiol and Levonorgestrel in Healthy Female Premenopausal Subjects

Completed
NCT02183493Phase 1

Bioavailability of BI 1356 Administered With and Without Food to Healthy Male and Female Subjects

Completed
NCT02183389Phase 1

Bioavailability of Warfarin After Coadministration With Multiple Doses of BI 1356 Compared to the Bioavailability of Warfarin Alone in Healthy Male Volunteers

Completed
NCT00819091Phase 3

Randomized, Double-blind (db), Placebo-controlled 18 Week Study of Linagliptin (BI 1356) in Type 2 Diabetic Patients With Insufficient Glycaemic Control on a Sulfonylurea Drug

Completed
NCT00800683Phase 3

Safety and Efficacy in Type 2 Diabetic Patients With Severe Chronic Renal Impairment, 5 mg BI 1356 (Linagliptin) vs. Placebo, Insulin Background Inclusive

Completed
NCT00622284Phase 3

Efficacy and Safety of BI 1356 in Combination With Metformin in Patients With Type 2 Diabetes

Completed
NCT00798161Phase 3

Safety and Efficacy of Linagliptin (BI 1356) Plus Metformin in Type 2 Diabetes, Factorial Design

Completed
NCT00654381Phase 3

Japanese P III vs Voglibose and Placebo

Completed

All 14 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
14