Success Metrics

Clinical Success Rate
95.2%

Based on 20 completed trials

Completion Rate
95%(20/21)
Active Trials
0(0%)
Results Posted
35%(7 trials)
Terminated
1(3%)

Phase Distribution

Ph not_applicable
3
10%
Ph phase_1
9
31%
Ph phase_3
7
24%
Ph phase_4
8
28%

Phase Distribution

9

Early Stage

0

Mid Stage

15

Late Stage

Phase Distribution27 total trials
Phase 1Safety & dosage
9(33.3%)
Phase 3Large-scale testing
7(25.9%)
Phase 4Post-market surveillance
8(29.6%)
N/ANon-phased studies
3(11.1%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

95.2%

20 of 21 finished

Non-Completion Rate

4.8%

1 ended early

Currently Active

0

trials recruiting

Total Trials

29

all time

Status Distribution
Completed(20)
Terminated(1)
Other(8)

Detailed Status

Completed20
unknown8
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
29
Active
0
Success Rate
95.2%
Most Advanced
Phase 4

Trials by Phase

Phase 19 (33.3%)
Phase 37 (25.9%)
Phase 48 (29.6%)
N/A3 (11.1%)

Trials by Status

terminated13%
completed2069%
unknown828%

Recent Activity

Clinical Trials (29)

Showing 20 of 29 trialsScroll for more
NCT04872400Phase 4

Acute Application of Antibiotic Powder in Open Fracture Wounds

Completed
NCT02526004Not Applicable

Cystic Fibrosis Microbiome-determined Antibiotic Therapy Trial in Exacerbations: Results Stratified

Completed
NCT05429671Phase 3

Antibiotic Loaded Cement After TKA

Completed
NCT03705962Phase 3

Locally Applied Antibiotics for Infection Prophylaxis in Treatment of Open Fractures

Terminated
NCT02918409Phase 4

IV Colistin for Pulmonary Exacerbations: Improving Safety and Efficacy

Completed
NCT02873806Phase 4

Two Trabecular Micro-bypass Stents & Postoperative Travoprost to Treat Glaucoma Subjects on Two Hypotensive Agents

Completed
NCT03673956Phase 1

Topical Antibiotics in Chronic Rhinosinusitis

Completed
NCT05313828

Effect of Various Treatment Modalities on Dendritic Vial Ulcer

Unknown
NCT03485456Phase 1

DPI-Tobra-Kind Cyclops® in Children With Cystic Fibrosis

Unknown
NCT03904836Phase 1

Tobramycin Administered at the Beginning of Dialysis

Completed
NCT01111383Phase 3

A Single Arm 48-Week Follow-on Safety Study to a Core Study Comparing the Efficacy and Tolerability of Tobrineb®/Actitob®/Bramitob® Versus TOBI®

Completed
NCT03308253Phase 4

Study for Antibiotic Impregnated Calcium Sulfate Beads as Prophylaxis for Surgical Site Infection

Unknown
NCT02207426Phase 1

Pharmacokinetic and Pharmacoscintigraphic Comparison of TobrAir® 6.0 With TOBI® and TOBI® Podhaler™

Completed
NCT00634192Phase 3

Pharmacokinetic Evaluation of an 8 -Week Treatment With Inhaled Tobramycin

Completed
NCT02269969Phase 1

Once Daily Aminoglycoside Pharmacokinetics and Optimal Dosing in the Burn Population: A Prospective Study

Completed
NCT02489955Not Applicable

Antibiotic Nephrotoxicity in Adult Patients With Cystic Fibrosis

Unknown
NCT00004829Phase 3

Phase III Randomized Study of the Inhalation of Tobramycin in Patients With Cystic Fibrosis

Completed
NCT00705159Phase 4

Safety and Efficacy of Zylet vs Lotemax, Tobramycin and Vehicle in Pediatric Blepharoconjunctivitis

Completed
NCT02035488Phase 1

Pharmacokinetic Evaluation and Tolerability of Dry Powder Tobramycin by a Novel Device in Patients With Non Cystic Fibrosis Bronchiectasis

Completed
NCT01155999Phase 3

Clinical Efficacy and Safety of T1225 Versus Tobramycin 0.3 % Eye Drops in the Treatment of Purulent Bacterial Conjunctivitis of Children.

Completed

Drug Details

Intervention Type
DRUG
Total Trials
29