Success Metrics

Clinical Success Rate
95.8%

Based on 23 completed trials

Completion Rate
96%(23/24)
Active Trials
1(4%)
Results Posted
30%(7 trials)
Terminated
1(4%)

Phase Distribution

Ph phase_4
1
4%
Ph phase_1
14
52%
Ph phase_3
3
11%
Ph not_applicable
5
19%
Ph phase_2
4
15%

Phase Distribution

14

Early Stage

4

Mid Stage

4

Late Stage

Phase Distribution27 total trials
Phase 1Safety & dosage
14(51.9%)
Phase 2Efficacy & side effects
4(14.8%)
Phase 3Large-scale testing
3(11.1%)
Phase 4Post-market surveillance
1(3.7%)
N/ANon-phased studies
5(18.5%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

88.5%

23 of 26 finished

Non-Completion Rate

11.5%

3 ended early

Currently Active

1

trials recruiting

Total Trials

27

all time

Status Distribution
Active(1)
Completed(23)
Terminated(3)

Detailed Status

Completed23
Withdrawn2
Recruiting1
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
27
Active
1
Success Rate
95.8%
Most Advanced
Phase 4

Trials by Phase

Phase 114 (51.9%)
Phase 24 (14.8%)
Phase 33 (11.1%)
Phase 41 (3.7%)
N/A5 (18.5%)

Trials by Status

withdrawn27%
completed2385%
recruiting14%
terminated14%

Recent Activity

Clinical Trials (27)

Showing 20 of 27 trialsScroll for more
NCT05571878Not Applicable

Is Brain Insulin Resistance a Feature of the Biology of Depression in Adolescents

Completed
NCT06532461Not Applicable

A Trial of Three- and Seven-days Insulin Infusions Set

Recruiting
NCT06153329Phase 1

A Trial to Evaluate the Pharmacokinetics and Pharmacodynamics of THDB0206 Injection in Healthy Chinese Subjects

Completed
NCT03262116Phase 2

Individualizing Automated Closed Loop Glucose Control Through Pharmacokinetic Profiling in an Insulin-Only Bionic Pancreas

Terminated
NCT04254380Phase 3

Gan & Lee Evaluation of New Biosimilar for Type 1 Lispro

Withdrawn
NCT03916640Phase 1

A Trial to Assess a Co-formulation of an Insulin Analog and Pramlintide in Subjects With Type 1 Diabetes Mellitus

Completed
NCT00705536Phase 1

Pharmacokinetic (PK), Pharmacodynamic (PD), and Safety Study of Subcutaneously Administered Humalog® With and Without Recombinant Human Hyaluronidase (rHuPH20)and Humulin-R® With and Without rHuPH20

Completed
NCT00774800Phase 2

Phase II Pharmacokinetics Study of Humalog and Humulin-R With and Without rHuPH20 in Type 1 Diabetes Mellitus

Completed
NCT03512236Phase 1

A Trial to Investigate Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of BioChaperone® Pramlintide Insulin in Patients With Type 1 Diabetes Mellitus

Completed
NCT03102476Not Applicable

Environmental Effects Type 1 Diabetes Mellitus

Completed
NCT03604575Not Applicable

A Study to Compare Pharmacokinetics and Pharmacodynamics of Insulin Lispro to Humalog® in Healthy Subjects

Completed
NCT02273180Phase 3

Comparison of SAR342434 to Humalog as the Rapid Acting Insulin in Adult Patients With Type 1 Diabetes Mellitus Also Using Insulin Glargine

Completed
NCT02294474Phase 3

Comparison of SAR342434 to Humalog as the Rapid Acting Insulin in Adult Patients With Type 2 Diabetes Mellitus Also Using Insulin Glargine

Completed
NCT02915250Phase 1

A Trial to Compare Post Prandial Blood Glucose Control of BioChaperone® Combo With Humalog® Mix25 and With Simultaneous Injections of Humalog® and Lantus® in Subjects With Type 2 Diabetes

Completed
NCT02213146Phase 1

A Double-blinded, Randomised, Three-period Crossover Euglycaemic Clamp Trial Investigating the Pharmacokinetics, Glucodynamics and Safety of BioChaperone Human Insulin, Human Insulin (Huminsulin® Normal) and Insulin Lispro (Humalog®) in Subjects With Type 1 Diabetes

Completed
NCT02344992Phase 1

Blood Glucose Control With BioChaperone Insulin Lispro Compared to Insulin Lispro (Humalog®) After Ingestion of a Standardized Meal

Completed
NCT02029924Phase 1

A Double-blinded, Randomised, Two -Period Crossover Euglycemic Clamp Trial Investigating the Pharmacokinetics, Glucodynamics and Safety of BioChaperone Insulin Lispro and Insulin Lispro (Humalog®) in Subjects With Type 1 Diabetes

Completed
NCT01971047Phase 4

Safety and Efficacy Study of Correcting Hyperglycemia in Patients With Diabetes Having Out-patient Surgery

Withdrawn
NCT02562313Phase 1

A Trial Investigating the Continuous Subcutaneous Insulin Infusion of a Liquid Formulation of BioChaperone Insulin Lispro in Comparison to Humalog®

Completed
NCT02660502Phase 1

An Euglycemic Clamp Trial to Evaluate Pharmacokinetics of Single Doses of BioChaperone Insulin Lispro in Healthy Japanese Subjects

Completed

Drug Details

Intervention Type
DRUG
Total Trials
27