Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 45/100

Failure Rate

23.5%

4 terminated/withdrawn out of 17 trials

Success Rate

76.5%

-10.0% vs industry average

Late-Stage Pipeline

35%

6 trials in Phase 3/4

Results Transparency

69%

9 of 13 completed trials have results

Key Signals

9 with results

Enrollment Performance

Analytics

Phase 2
6(35.3%)
Phase 3
6(35.3%)
Phase 1
5(29.4%)
17Total
Phase 2(6)
Phase 3(6)
Phase 1(5)

Activity Timeline

Global Presence

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Clinical Trials (17)

Showing 17 of 17 trials
NCT00983814Phase 2Completed

Study of Droxidopa Treatment in Adults With Attention Deficit Hyperactivity Disorder With Co-administration of Carbidopa

Role: lead

NCT01323374Phase 2Completed

Study To Assess The Clinical Benefit Of Droxidopa And Droxidopa/Carbidopa In Subjects With Fibromyalgia

Role: lead

NCT01132326Phase 3Completed

Clinical Study of Droxidopa in Patients With Neurogenic Orthostatic Hypotension (NOH) (Droxi-304)

Role: lead

NCT01927055Phase 3Terminated

A Clinical Study of Patients With Symptomatic NOH to Assess Sustained Effects of Droxidopa Therapy

Role: lead

NCT00657046Phase 2Completed

Safety and Benefit Study of Droxidopa to Treat Patients With Intradialytic Hypotension

Role: lead

NCT00977171Phase 2Terminated

Study To Assess The Clinical Benefit Of Droxidopa In Subjects With Chronic Fatigue Syndrome

Role: lead

NCT01176240Phase 3Completed

A Two Part Study (306A/306B) to Assess Droxidopa in Treatment of NOH in Patients With Parkinson's Disease

Role: lead

NCT00633880Phase 3Completed

Clinical Study of Droxidopa in Patients With Neurogenic Orthostatic Hypotension (NOH)

Role: lead

NCT00738062Phase 3Completed

Open-Label Clinical Study of Droxidopa in Patients With Neurogenic Orthostatic Hypotension (NOH)

Role: lead

NCT00782340Phase 3Completed

A Clinical Study for Patients With Neurogenic Orthostatic Hypotension (NOH) Using Droxidopa

Role: lead

NCT01354158Phase 1Completed

A Dose Titration of Droxidopa in Patients With Spinal Cord Injury

Role: collaborator

NCT01116141Phase 2Completed

A Study of CH-4051 in Patients With Rheumatoid Arthritis (RA)

Role: lead

NCT00658047Phase 2Completed

A Study to Assess CH1504 in Patients With Active Rheumatoid Arthritis

Role: lead

NCT01468259Phase 1Withdrawn

A Multi-Center, Open-Label Study

Role: lead

NCT01331122Phase 1Withdrawn

Study to Assess Droxidopa in the Treatment of Freezing Of Gait Symptoms in Patients With Parkinson's Disease

Role: lead

NCT01149629Phase 1Completed

Study of the Fed-Fast Pharmocokinetics and Bioequivalance of 300mg Capsules of Droxidopa

Role: lead

NCT01327066Phase 1Completed

Electrocardiographic (ECG) Safety Study of Droxidopa at Clinical and Supratherapeutic Dose

Role: lead

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