Success Metrics

Clinical Success Rate
92.5%

Based on 270 completed trials

Completion Rate
92%(270/292)
Active Trials
26(7%)
Results Posted
61%(165 trials)
Terminated
22(6%)

Phase Distribution

Ph phase_4
10
3%
Ph early_phase_1
1
0%
Ph phase_1
55
16%
Ph phase_3
123
35%
Ph not_applicable
15
4%
Ph phase_2
145
41%

Phase Distribution

56

Early Stage

145

Mid Stage

133

Late Stage

Phase Distribution349 total trials
Early Phase 1First-in-human
1(0.3%)
Phase 1Safety & dosage
55(15.8%)
Phase 2Efficacy & side effects
145(41.5%)
Phase 3Large-scale testing
123(35.2%)
Phase 4Post-market surveillance
10(2.9%)
N/ANon-phased studies
15(4.3%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

88.2%

270 of 306 finished

Non-Completion Rate

11.8%

36 ended early

Currently Active

26

trials recruiting

Total Trials

350

all time

Status Distribution
Active(34)
Completed(270)
Terminated(36)
Other(10)

Detailed Status

Completed270
Terminated22
Recruiting16
Withdrawn14
Active, not recruiting10
unknown9

Development Timeline

Analytics

Development Status

Total Trials
350
Active
26
Success Rate
92.5%
Most Advanced
Phase 4

Trials by Phase

Early Phase 11 (0.3%)
Phase 155 (15.8%)
Phase 2145 (41.5%)
Phase 3123 (35.2%)
Phase 410 (2.9%)
N/A15 (4.3%)

Trials by Status

recruiting165%
terminated226%
active_not_recruiting103%
suspended10%
withdrawn144%
enrolling_by_invitation10%
unknown93%
completed27077%
not_yet_recruiting72%

Recent Activity

Clinical Trials (350)

Showing 20 of 350 trialsScroll for more
NCT03502434Phase 1

A Repeat Insult Patch Test (RIPT) Study Evaluating the Sensitization Potential of Topical SM04755 Solution in Healthy Volunteers

Completed
NCT07838129Phase 4

Evaluation of Corneal Endothelium Health Following Articaine Ophthalmic Solution Administration

Not Yet Recruiting
NCT07395232Phase 3

An Efficacy and Safety Study of DFL24498 in the Treatment of AKC

Recruiting
NCT05586152Phase 1

Study of INV-102 Ophthalmic Solution in Adults With Moderate Symptomatic Dry Eye Disease

Completed
NCT05636228Phase 2

Study of INV-102 Ophthalmic Solution in Adults With Acute Infectious Keratoconjunctivitis

Completed
NCT06370039Phase 2

Study of INV-102 Ophthalmic Solution in Adults With Moderate to Severe Dry Eye Disease

Completed
NCT06164743Phase 2

Phase 2: VVN461 Ophthalmic Solution for Post -Operative Ocular Inflammation After Cataract Surgery

Completed
NCT07453888Phase 3

Efficacy and Safety of Intranasal Cenegermin in Adult Participants With Non-Arteritic Anterior Ischemic Optic Neuropathy (NAION)

Recruiting
NCT07355075Phase 2

A Double-Blind, Randomized, Vehicle-Controlled Phase 2 Study to Assess the Efficacy and Safety of GX-03 in Adult Subjects With Moderate to Severe Atopic Dermatitis (Eczema)

Recruiting
NCT05565950Phase 1

AI-09 In Subjects With Glabellar Lines, GL-101

Completed
NCT07578363Phase 3

An Investigation of FID 123472 Ophthalmic Solution to Vehicle for the Reduction of Ocular Redness in Adults

Not Yet Recruiting
NCT07531043Phase 3

Efficacy and Safety of FID 123472 Ophthalmic Solution for Ocular Redness in Adults

Not Yet Recruiting
NCT05688904Phase 1

The Effect of Topical Imipramine on Pain and Effectiveness of Topical Photodynamic Therapy

Recruiting
NCT06195605Not Applicable

Investigating Age Dependence of Fibroblast and Extracellular Matrix Responses to Cross-linked Hyaluronic Acid Filler in Human Skin

Active Not Recruiting
NCT00744211Not Applicable

Proteolytic Enzyme Induction Within the Human Myocardial Interstitium

Completed
NCT06128369Phase 3

A Phase 3 Study Evaluating the Efficacy and Safety of OCS-01 Opthalmic Suspension Compared to Vehicle for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery

Terminated
NCT03918915Phase 3

The Safety and Efficacy of SYD-101 in Children With Myopia

Completed
NCT07519902Phase 3

An Efficacy and Safety Study of Cenegermin Ophthalmic Solution Compared With Vehicle in the Treatment of PCED

Recruiting
NCT07128628Phase 2

A Study Evaluating the Safety and Efficacy of a Fixed-Dose Combination for Dry Eye Disease

Completed
NCT06073132Phase 2

An International, Multicenter, Randomized, Double-Blind, Parallel Group, Vehicle-Controlled, Phase 2/3 Study With Open-Label Extension Evaluating the Efficacy and Safety of Diacerein 1% Ointment for the Treatment of Generalized Epidermolysis Bullosa Simplex (EBS)

Active Not Recruiting

Drug Details

Intervention Type
OTHER
Total Trials
350