Key Insights

Highlights

Success Rate

78% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 39/100

Termination Rate

9.5%

2 terminated out of 21 trials

Success Rate

77.8%

-8.7% vs benchmark

Late-Stage Pipeline

14%

3 trials in Phase 3/4

Results Transparency

43%

3 of 7 completed with results

Key Signals

3 with results78% success

Data Visualizations

Phase Distribution

14Total
Not Applicable (5)
P 1 (5)
P 2 (1)
P 3 (2)
P 4 (1)

Trial Status

Completed7
Unknown6
Withdrawn3
Not Yet Recruiting2
Terminated2
Recruiting1

Trial Success Rate

77.8%

Benchmark: 86.5%

Based on 7 completed trials

Clinical Trials (21)

Showing 20 of 20 trials
NCT06926478Phase 1Not Yet Recruiting

Subconjunctival Humira for Boston Keratoprosthesis

NCT03585946WithdrawnPrimary

Outcomes in Stevens Johnsons Syndrome and Toxic Epidermal Necrolysis

NCT02987257Phase 3CompletedPrimary

NATIENS: Optimal Management and Mechanisms of SJS/TEN

NCT04313725Not ApplicableTerminatedPrimary

Evaluation of Tangible Boost for Patients With Stevens Johnson Syndrome, Sjogren's Syndrome, and Graft Vs Host Disease

NCT06474078Not ApplicableCompletedPrimary

Study To Evaluate The Efficacy Of Tofacitinib In Patients With SJS/TEN

NCT07014059Phase 2Not Yet Recruiting

Autologous Serum Obtained by a Closed-Circuit Collection Device

NCT02945176Not ApplicableCompleted

Safety and Performance Study of the ARGOS-IO System in Patients Undergoing Boston Keratoprosthesis Implantation

NCT05520086Phase 1Unknown

Clinical Trial to Evaluate Safety and Efficacy of Cell Therapy in Patients With Cicatricial Conjuntivitis.

NCT06263140CompletedPrimary

Vitamin D Levels in Non-immediate Drug Hypersensitivity Case-control Study

NCT03659227RecruitingPrimary

Drug Reactions Sampling (COLLECTIONTOXIDERMIES)

NCT05284929Unknown

Human Leukocyte Antigen Class II (DRB1 and DQB1) Alleles and Haplotypes Frequencies in Patients With Pemphigus Vulgaris Among the Russian Population

NCT05145959Not ApplicableUnknownPrimary

Meibomian Gland Probing in the Sub-Acute Phase of Patients With Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis

NCT02126020Phase 1WithdrawnPrimary

Topical Infliximab in Autoimmune Eyes With Keratoprosthesis

NCT03046914Not ApplicableUnknownPrimary

HLA-B*5801 Screening to Prevent Allopurinol-induced Severe Cutaneous Adverse Reaction

NCT02037347Phase 1Terminated

Study to Evaluate the Use of Palifermin to Treat Toxic Epidermal Necrolysis

NCT02149732Unknown

Clinical Trial on the Effect of Autologous Oral Mucosal Epithelial Sheet Transplantation

NCT01256489Phase 1WithdrawnPrimary

Infliximab to Improve Retention of the Boston Keratoprosthesis in Patients After Stevens Johnson Syndrome/ Toxic Epidermal Necrolysis (SJS/TENS)

NCT01696500Phase 3CompletedPrimary

Phase III Clinical Trial of NPB-01 in Patients With Stevens-Johnson Syndrome/ Toxic Epidermal Necrolysis Unresponsive to Corticosteroids.

NCT01488396Phase 4CompletedPrimary

Efficacy of 0.05% Cyclosporin Eye Drop in Stevens Johnson Syndrome Patient With Chronic Dry Eye

NCT01122303UnknownPrimary

Corneal Epitheliotropic Factors in Autologous Serum Eye Drops in Nonautoimmune and Stevens-Johnson Syndrome With Dry Eye

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