Success Metrics

Clinical Success Rate
84.8%

Based on 28 completed trials

Completion Rate
85%(28/33)
Active Trials
2(4%)
Results Posted
32%(9 trials)
Terminated
5(11%)

Phase Distribution

Ph phase_4
11
24%
Ph phase_2
11
24%
Ph not_applicable
8
18%
Ph phase_1
7
16%
Ph phase_3
8
18%

Phase Distribution

7

Early Stage

11

Mid Stage

19

Late Stage

Phase Distribution45 total trials
Phase 1Safety & dosage
7(15.6%)
Phase 2Efficacy & side effects
11(24.4%)
Phase 3Large-scale testing
8(17.8%)
Phase 4Post-market surveillance
11(24.4%)
N/ANon-phased studies
8(17.8%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

82.4%

28 of 34 finished

Non-Completion Rate

17.6%

6 ended early

Currently Active

2

trials recruiting

Total Trials

45

all time

Status Distribution
Active(2)
Completed(28)
Terminated(6)
Other(9)

Detailed Status

Completed28
unknown9
Terminated5
Recruiting2
Withdrawn1

Development Timeline

Analytics

Development Status

Total Trials
45
Active
2
Success Rate
84.8%
Most Advanced
Phase 4

Trials by Phase

Phase 17 (15.6%)
Phase 211 (24.4%)
Phase 38 (17.8%)
Phase 411 (24.4%)
N/A8 (17.8%)

Trials by Status

recruiting24%
terminated511%
unknown920%
withdrawn12%
completed2862%

Recent Activity

Clinical Trials (45)

Showing 20 of 45 trialsScroll for more
NCT02390284Phase 3

Stop Retinal Ganglion Cell Dysfunction Study

Terminated
NCT06666855Phase 3

A Phase III Study in Subjects With Primary Open Angle Glaucoma or Ocular Hypertension in China

Recruiting
NCT06239324Phase 1

Evaluation of Latanoprost Combined With Fractional Erbium- YAG Laser

Recruiting
NCT00579969Phase 2

Comparison of Latanoprost Vs. Timolol

Terminated
NCT00572936Phase 2

Circadian Rhythms of Aqueous Humor Dynamics in Humans

Completed
NCT04811326Phase 4

Latanoprost Plus NB-UVB Versus Each Alone in Non-segmental Vitiligo: Clinical and Laboratory Evaluation

Unknown
NCT00934089Phase 2

A Phase 2 Study Of The 24-Hour Intraocular Pressure Lowering And Systemic Exposure Of PF-04217329

Completed
NCT04737928Not Applicable

Prospective, Single Center Switching Study of 0.0015% Tafluprost Ophthalmic Solution in Primary Open-angle Glaucoma and Ocular Hypertension Patients With Corneal Disorders (Switching From 0.005% Latanoprost Ophthalmic Solution)

Completed
NCT00716859Phase 3

A Phase 3 Prospective, Randomized, Double-Masked, 12-Week, Parallel Group Study In Pediatric Subjects With Glaucoma.

Completed
NCT00647101Phase 4

A Study to Assess the Efficacy of 3 Months of Latanoprost Treatment in Reducing the Intraocular Pressure in Patients With Ocular Hypertension or Open-angle Glaucoma

Completed
NCT00638742Phase 1

A Phase 1, Open-Label Study of Latanoprost Acid Plasma Concentrations in Pediatric and Adult Glaucoma Patients Treated With Latanoprost.

Completed
NCT00846989Phase 1

Efficacy, Tolerability and Safety of RKI983 (0.05% & 0.10%) vs Xalatan in Patients With POAG or Ocular Hypertension

Completed
NCT04178863Phase 4

CATS Tonometer IOP Reduction Latanoprost Verses Timolol

Unknown
NCT03419975Phase 3

A Multi-center, Randomized, Blinded Evaluator, Active Control, Parallel, Phase III Study to Evaluate the Efficacy and Safety of TJO-002 in POAG or Ocular Hypertension Patients

Completed
NCT02656979Not Applicable

Blood Flow of Ophthalmic Artery and Glaucoma

Unknown
NCT03966560Phase 4

Choroidal Thickness and Its Correlations With Ocular Parameters in Primary Open-angle Glaucoma

Completed
NCT03762369Phase 3

A Clinical Study to Evaluate the Efficacy and Safety of CKD-351

Unknown
NCT03611348Phase 2

Microneedling and Latanoprost in Acrofacial Vitiligo

Unknown
NCT03480906Not Applicable

Eyenovia MiDD Usability Study

Completed
NCT01223378Phase 2

Study Comparing the Safety and Efficacy of BOL-303259-X to Latanoprost in Subjects With Glaucoma or Ocular Hypertension

Completed

Drug Details

Intervention Type
DRUG
Total Trials
45