Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

High Risk

Score: 80/100

Failure Rate

35.3%

6 terminated/withdrawn out of 17 trials

Success Rate

57.1%

-29.4% vs industry average

Late-Stage Pipeline

6%

1 trials in Phase 3/4

Results Transparency

163%

13 of 8 completed trials have results

Key Signals

2 recruiting13 with results6 terminated

Enrollment Performance

Analytics

N/A
14(93.3%)
Phase 4
1(6.7%)
15Total
N/A(14)
Phase 4(1)

Activity Timeline

Global Presence

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Clinical Trials (17)

Showing 17 of 17 trials
NCT07365735Not ApplicableActive Not Recruiting

TearCare MGX™ System With and Without Warming Hold

Role: lead

NCT06991270Not ApplicableRecruiting

OMNI 3.1 Surgical System in Subjects With Primary Open-Angle Glaucoma

Role: lead

NCT04795752Not ApplicableCompleted

Safety And Effectiveness Of The TearCare® System In The Treatment Of The Signs And Symptoms Of Dry Eye Disease (SAHARA)

Role: lead

NCT02928289Not ApplicableTerminated

Safety and Effectiveness of the Sight Sciences VISCO™360 Versus SLT in Primary Open Angle Glaucoma

Role: lead

NCT03804502Not ApplicableCompleted

Pilot Study of TearCare System - Long-Term Extension

Role: lead

NCT04658095Not ApplicableTerminated

Study of OMNI Surgical System and iStent for Eyes With OAG (Trident)

Role: lead

NCT03006978Not ApplicableCompleted

A Pilot Study of the TearCare System in Adults With Dry Eye Disease

Role: lead

NCT03857919Not ApplicableCompleted

TearCare System to Treat Dry Eye Disease

Role: lead

NCT03502447Not ApplicableTerminated

Randomized Study of the Safety and Effectiveness of the TearCare System for the Signs and Symptoms of Dry Eye Disease

Role: lead

NCT03588624Not ApplicableCompleted

Study of the TearCare System in Dry Eye Disease

Role: lead

NCT06948773Not ApplicableRecruiting

A Study of the Helix Surgical System in Primary Open-Angle Glaucoma (POAG) and Cataract (HELIX)

Role: lead

NCT04872348Completed

An Observational Multicenter Clinical Study To Assess The Safety And Effectiveness Of The OMNI® Surgical System In Pseudophakic Eyes With Primary Open Angle Glaucoma (ORION 2.0)

Role: lead

NCT06407973Phase 4Terminated

A Clinical Trial Comparing the OMNI Surgical System to Standard Medical Treatment in Patients With Primary Open Angle Glaucoma

Role: lead

NCT05044793Completed

A Clinical Study To Assess The Safety And Effectiveness Of The OMNI® Surgical System

Role: lead

NCT03861169Not ApplicableCompleted

Study of OMNI System in OAG (GEMINI)

Role: lead

NCT04616573Not ApplicableTerminated

A Post-market Study Of Use Of The OMNI® Surgical System In Open Angle Glaucoma

Role: lead

NCT04465630Not ApplicableTerminated

A Prospective, Multicenter Study of the OMNI® Surgical System in Pseudophakic Eyes With Open Angle Glaucoma

Role: lead

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