Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 35/100

Failure Rate

4.5%

1 terminated/withdrawn out of 22 trials

Success Rate

95.5%

+8.9% vs industry average

Late-Stage Pipeline

23%

5 trials in Phase 3/4

Results Transparency

24%

5 of 21 completed trials have results

Key Signals

5 with results

Enrollment Performance

Analytics

Phase 2
13(59.1%)
Phase 3
5(22.7%)
Phase 1
4(18.2%)
22Total
Phase 2(13)
Phase 3(5)
Phase 1(4)

Activity Timeline

Global Presence

Loading network data...

Clinical Trials (22)

Showing 20 of 22 trials
NCT01868516Phase 2Completed

Study Evaluating the Safety, Tolerability, and Efficacy of Dexmecamylamine (TC-5214) for Treatment of Overactive Bladder

Role: lead

NCT01488929Phase 2Completed

Efficacy, Safety, and Tolerability of TC-5619 as Augmentation Therapy to Improve Negative Symptoms and Cognition in Outpatients With Schizophrenia

Role: lead

NCT01466088Phase 2Completed

Efficacy, Safety, & Tolerability of AZD3480 Patients With Mild to Moderate Dementia of the Alzheimer's Type (AD)

Role: lead

NCT02187094Phase 1Completed

Study Evaluating the Effect of TC-6499 on Gastric Emptying Time in Diabetic Subjects With Gastroparesis

Role: lead

NCT01157078Phase 3Completed

A Study to Assess the Efficacy and Safety of TC-5214 as an Adjunct Therapy in Patients With Major Depressive Disorder (MDD)

Role: collaborator

NCT01197508Phase 3Completed

A Study to Assess the Efficacy and Safety of TC-5214 as an Adjunct Therapy in Patients With Major Depressive Disorder.

Role: collaborator

NCT01153347Phase 3Completed

A Study to Assess the Efficacy and Safety of TC-5214 as an Adjunct Therapy in Patients With Major Depressive Disorder

Role: collaborator

NCT01152554Phase 3Completed

A Study to Assess the Long- Term Safety of TC-5214 as an Adjunct Therapy in Patients With Major Depressive Disorder

Role: collaborator

NCT01180400Phase 3Completed

A Study to Assess the Efficacy and Safety of TC-5214 as an Adjunct Therapy in Patients With Major Depressive Disorder

Role: collaborator

NCT01149200Phase 2Completed

Proof-of-Principle Study of TC-6499 in the Treatment of Constipation Predominant Irritable Bowel Syndrome (IBS)

Role: lead

NCT01003379Phase 2Completed

TC-5619 as Augmentation Therapy to Improve Cognition in Outpatients With Cognitive Dysfunction in Schizophrenia

Role: lead

NCT00899977Phase 1Terminated

TC-5214 as Augmentation Therapy in Patients With Refractory Hypertension

Role: lead

NCT01124708Phase 2Completed

Efficacy, Safety, and Tolerability of TC-5619 in Adults With Attention Deficit/Hyperactivity Disorder (ADHD)

Role: lead

NCT01293669Phase 2Completed

Glycemic Control, Safety and Tolerability of TC-6987 Monotherapy in Type 2 Diabetes Mellitus

Role: lead

NCT01296087Phase 2Completed

TC-6987 for the Treatment of Mild to Moderate Asthma

Role: lead

NCT01254448Phase 1Completed

Multiple Ascending Dose Study of TC-5619 in Healthy Elderly Subjects and Subjects With Alzheimer's Disease

Role: lead

NCT00692445Phase 2Completed

TC-5214 as add-on the Treatment of Major Depressive Disorder

Role: lead

NCT01472991Phase 2Completed

Safety & Efficacy of TC-5619 in Adults With Inattentive-predominant Attention Deficit/Hyperactivity Disorder (ADHD)

Role: lead

NCT00683462Phase 2Completed

An Exploratory Trial of AZD3480 (TC-1734) for the Treatment of Adult Attention-Deficit/Hyperactivity Disorder (ADHD)

Role: collaborator

NCT00109564Phase 2Completed

A Safety and Efficacy Study of Ispronicline (TC-1734-112) in Subjects With Age Associated Memory Impairment (AAMI)

Role: lead