Success Metrics

Clinical Success Rate
100.0%

Based on 17 completed trials

Completion Rate
100%(17/17)
Active Trials
0(0%)
Results Posted
18%(3 trials)

Phase Distribution

Ph phase_4
1
5%
Ph phase_2
9
47%
Ph not_applicable
3
16%
Ph phase_3
3
16%
Ph phase_1
2
11%

Phase Distribution

2

Early Stage

9

Mid Stage

4

Late Stage

Phase Distribution18 total trials
Phase 1Safety & dosage
2(11.1%)
Phase 2Efficacy & side effects
9(50.0%)
Phase 3Large-scale testing
3(16.7%)
Phase 4Post-market surveillance
1(5.6%)
N/ANon-phased studies
3(16.7%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

94.4%

17 of 18 finished

Non-Completion Rate

5.6%

1 ended early

Currently Active

0

trials recruiting

Total Trials

19

all time

Status Distribution
Completed(17)
Terminated(1)
Other(1)

Detailed Status

Completed17
Withdrawn1
unknown1

Development Timeline

Analytics

Development Status

Total Trials
19
Active
0
Success Rate
100.0%
Most Advanced
Phase 4

Trials by Phase

Phase 12 (11.1%)
Phase 29 (50.0%)
Phase 33 (16.7%)
Phase 41 (5.6%)
N/A3 (16.7%)

Trials by Status

withdrawn15%
unknown15%
completed1789%

Recent Activity

Clinical Trials (19)

Showing 19 of 19 trials
NCT04243629Not Applicable

Co-administration of Pramlintide and Insulin Via an Automated Dual-hormone Artificial Pancreas System in Adults With Type 1 Diabetes

Unknown
NCT04163874Not Applicable

Alleviating Carbohydrate Counting for Patients With Type 1 Diabetes Using a Novel Insulin-plus-pramlintide Artificial Pancreas

Completed
NCT00732147Not Applicable

Effects of Pramlintide on Endogenous Production of Very-low-density-lipoprotein (VLDL)-Triglyceride and Glucose in the Post Prandial State in T2DM

Withdrawn
NCT02500979Phase 1

Effect of a Fixed Pramlintide: Insulin Dose Ratio on Postprandial Glucose in Type 1 Diabetes Mellitus

Completed
NCT00042601Phase 2

Evaluation of the Effect of Pramlintide on Satiety and Food Intake

Completed
NCT00042458Phase 3

Evaluation of Dose-titration of Pramlintide During Initiation of Therapy in Patients Trying to Improve Glucose Control

Completed
NCT00042471Phase 2

Evaluation of the Bioavailability of Pramlintide

Completed
NCT00107107Phase 3

Study of the Long-Term Safety of Pramlintide in Subjects With Type 1 Diabetes Mellitus

Completed
NCT00444561Phase 2

Exploratory Study to Evaluate Various Pharmacodynamic Effects of Subcutaneously Infused or Injected Pramlintide in Obese Subjects

Completed
NCT00189514Phase 2

A Study to Examine the Long Term Effect of Pramlintide on Body Weight and Its Safety and Tolerability in Obese Subjects

Completed
NCT00108004Phase 3

Clinical Utility and Safety of Pramlintide in Subjects With Type 1 and Type 2 Diabetes Mellitus

Completed
NCT00044707Phase 2

Evaluation of an Orally Administered Medication When Taken in Conjunction With Pramlintide

Completed
NCT00673387Phase 2

Study to Examine Safety, Tolerability, and Effect on Body Weight of Metreleptin Administered in Conjunction With Pramlintide in Obese and Overweight Subjects

Completed
NCT00112021Phase 2

A Study to Examine the Effect of Pramlintide on Body Weight and Its Safety and Tolerability in Obese Subjects

Completed
NCT00240253Phase 4

A Study Evaluating the Efficacy and Safety of Adding Symlin® to Lantus® (Insulin Glargine) in Subjects With Type 2 Diabetes

Completed
NCT00229658

An Observational Study Evaluating SYMLIN® (Pramlintide Acetate) Injection Use in Insulin Using Patients With Type 2 and Type 1 Diabetes

Completed
NCT00313183Phase 2

A Study to Evaluate Symlin in Adolescent Subjects With Type 1 Diabetes Mellitus

Completed
NCT00402077Phase 2

A Study to Examine the Safety, Tolerability, and Body Weight Effect of Pramlintide Alone and in Combination With Oral Antiobesity Agents in Overweight and Obese Subjects

Completed
NCT01708044Phase 1

Effect of Different Fixed Pramlintide:Insulin Dose Ratios on Postprandial Glucose in T1DM

Completed

All 19 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
19